The promise(s) of mesenchymal stem cell therapy in averting preclinical diabetes: lessons from in vivo and in vitro model systems

Kotikalapudi, Nagasuryaprasad; Sampath, Samuel Joshua Pragasam; Sukesh Narayan, Sinha; R., Bhonde; Nemani, Harishankar; Mungamuri, Sathish Kumar; Venkatesan, Vijayalakshmi

doi:10.1038/s41598-021-96121-0

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Published: 20 August 2021

The promise(s) of mesenchymal stem cell therapy in averting preclinical diabetes: lessons from in vivo and in vitro model systems

Nagasuryaprasad Kotikalapudi¹,
Samuel Joshua Pragasam Sampath¹,
Sinha Sukesh Narayan²,
Bhonde R.³^nAff5,
Harishankar Nemani⁴,
Sathish Kumar Mungamuri² &
…
Vijayalakshmi Venkatesan¹

Scientific Reports volume 11, Article number: 16983 (2021) Cite this article

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An Author Correction to this article was published on 28 September 2021

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Abstract

Obesity (Ob) poses a significant risk factor for the onset of metabolic syndrome with associated complications, wherein the Mesenchymal Stem Cell (MSC) therapy shows pre-clinical success. Here, we explore the therapeutic applications of human Placental MSCs (P-MSCs) to address Ob-associated Insulin Resistance (IR) and its complications. In the present study, we show that intramuscular injection of P-MSCs homed more towards the visceral site, restored HOMA-IR and glucose homeostasis in the WNIN/GR-Ob (Ob-T2D) rats. P-MSC therapy was effective in re-establishing the dysregulated cytokines. We report that the P-MSCs activates PI3K-Akt signaling and regulates the Glut4-dependant glucose uptake and its utilization in WNIN/GR-Ob (Ob-T2D) rats compared to its control. Our data reinstates P-MSC treatment's potent application to alleviate IR and restores peripheral blood glucose clearance evidenced in stromal vascular fraction (SVF) derived from white adipose tissue (WAT) of the WNIN/GR-Ob rats. Gaining insights, we show the activation of the PI3K-Akt pathway by P-MSCs both in vivo and in vitro (palmitate primed 3T3-L1 cells) to restore the insulin sensitivity dysregulated adipocytes. Our findings suggest a potent application of P-MSCs in pre-clinical/Ob-T2D management.

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Introduction

Obesity presenting with insulin resistance (IR), impaired glucose tolerance (IGT), and hyperglyceridemia (HG) has posed as a significant public health concern linked to several comorbidities like cardiovascular diseases, hypertension, chronic kidney disease, Alzheimer's disease, and certain cancers^1,2. There has been an exponential increase in these associated metabolic pathologies, posing severe health threats worldwide, affecting over 40 to 50% of the adult population, because of which ~ 2.8 million people lose their lives globally every year^3,4. The critical determinant underlying this pathophysiological state attributes to the inflammatory milieu (enlarged adipose tissue and macrophage infiltration) with sustained release of pro-inflammatory cytokines (TNFα, IL-1β, and IL-6)^5,6, In addition, acute-phase cytokines and altered inflammatory signaling pathways in adipose tissue form a linking factor for several metabolic syndromes like Obesity and Type 2 Diabetes (Ob-T2D)². Adipose tissue is the major contributor for the circulating IL-1β, TNFα, IL-6 during obese conditions, wherein IL-1β receptors are shown to induce major inflammatory signaling kinases and transcriptional pathways that result in impaired insulin receptor functions and altered Glut4 translocation in adipose tissue^5,6. In obese people, the risk of T2D is primarily determined by the site of fat accumulation^7,8,9. Adipose tissue, skeletal muscle, liver, and brain to a lesser extent, etc., are the significant depots of fat accumulation. Excess free fatty acids (FFA) in the obese condition contribute to the IR observed in these target tissues resulting in altered energy homeostasis¹⁰. Obesity has been associated with high infiltration and accumulation of macrophages within the adipose tissue¹¹, and it is of utmost interest to note that macrophages can induce and secrete a range of pro-inflammatory cytokines that cause tissue inflammation and trigger the secretion of other pro-inflammatory molecules¹².

Current therapies widely being used for Ob-T2D includes metformin, wherein it lowers liver glucose production^13,14, besides its beneficial role in improving insulin sensitivity in the skeletal muscle^15,16, and in the at WAT^17,18. The other approved drugs for T2D include DPP-4 inhibitors, Sulfonylureas, and Meglitinides, whose treatment generally increases insulin secretion and/or glucose utilization^19,20, in addition to exogenous insulin application to effectively ameliorate hyperglycemia and also improve the insulin response in target tissues, but owes limitations of short-term duration. Recent advances in identifying stem cells, more so adult stem cells/mesenchymal stem cells (MSCs) have gained attention in regenerative research due to their inherent immunomodulatory, multilineage, self-renewal, and potent secretome functions. MSCs modulate their cellular microenvironment, activate endogenous/resident progenitor cells, and secrete various factors²¹, and appear to hold promise(s) to improve healthcare by either augmenting body's own regenerative potential, such as in wound healing, ischemic diseases, neurological disorders, and diabetes mellitus, or development of new therapies²². The therapeutic effects of MSCs have been reported in diabetic subjects, diabetic models²³ showing that MSCs could lower blood glucose levels. Other strategies to promote β-cell regeneration/repopulation vis-à-vis overcome IR in the target tissues (muscle/adipose) also open up alternate options for the management of T2D. Despite several options, the precise mechanism(s) underlying these effects are still obscure.

The impetus obtained from our earlier studies^24,25, and other related studies portrays Ob-T2D as a state of profound stress and inflammation^5,6. Interestingly, immunomodulatory effects of the human placental mesenchymal stem cells (P-MSCs) to blunt inflammatory response and allow tissue remodeling after injury^26,27 reinstate their efficacy for safe transplantation. Recently, the promise(s) of Wharton's Jelly-derived MSCs to differentiate into islet-like clusters (ILCs)²⁸, P-MSCs into ILCs²² have renewed interest for several β-cell researchers. The efficacy and feasibility of MSC therapy in obesity-induced pre-clinical diabetic conditions, interfacing with the onset of chronic diseases, have not been explored to date.

In the present study, we aim to explore the possible therapeutic efficacy of P-MSCs using WNIN/GR-Ob (Ob-T2D) rats as they portray both obesity & diabetic-related phenotype with IR^24,25,26,27, developed indigenously at the National Center for Laboratory Animals Science (NCLAS) facility of ICMR-National Institute of Nutrition (NIN). They also show accelerated aging with a reduced average life span being 1.5 years compared to 2.5–3 years seen in the controls^24,25,26,27. In the present study, we report for the first time the beneficial effects of P-MSCs treatment in WNIN/GR-Ob (Ob-T2D) mutant rats, depicting pre-clinical/clinical T2D and presents with frank obesity, IR, lean body mass, higher fat mass, hyper-insulinemia, hyper-triglyceridemia, hyper-cholesterolemia, and hyper-leptinemia, akin to human subjects of obesity/obesity-induced T2D. To pin down the mechanistic insights of P-MSCs in situ, we carried out in vitro experiments with adipocytes derived from palmitate primed 3T3-L1 cells and co-cultured with and without P-MSCs to assess the beneficial effects of P-MSCs.

We hypothesize that intramuscular injections of P-MSCs to WNIN/GR-Ob (Ob-T2D) rats with IR would ameliorate the obesogenic milieu in adipose tissue and counter the IR. These injections are likely to modulate the microenvironment/niche of adipose tissue to modulate adipokine secretions so as to blunt inflammation vis-à-vis enhance glucose sensitivity via Glut4 translocation to overcome IR. To test our hypothesis, we aim to explore the possible therapeutic efficacy of P-MSCs using WNIN/GR-Ob (Ob-T2D) rats studied in both subcutaneous and visceral depots and compare them with WNIN/Controls to evaluate) glycaemic status (IGTT, ITT, HOMA-IR), cytokine profiling, insulin signaling, metabolites, and Glut4 transportation and translocation.

Results

In vitro characterization of P-MSCs

Human P-MSCs were isolated from the placenta's chorionic side, which was highly proliferative, and showed colony-forming units in the bright field microscope (Fig. 1a). These cells were positive for CD133, STRO-1, CD90, and CD105 and were negative for CD34. P-MSCs demonstrated multilineage capacity and differentiated into adipogenic, chondrogenic, and osteogenic lineages, when cultured in appropriate differentiation conditions. These results support their mesenchymal phenotype (Fig. 1b,c).

P-MSCs home to the visceral region in WNIN/GR-Ob (Ob-T2D) rats

We next studied the homing capacity of P-MSCs to assess their migration in WNIN/Control and WNIN/GR-Ob (Ob-T2D) rats. We intramuscularly injected the P-MSCs (1 × 10⁶ in 100 µl 1× PBS), that were labeled with DiD (DilC₁₈(5) solid (1,1′-Dioctadecyl-3,3,3′,3′-Tetramethylindodicarbocyanine, 4-Chlorobenzenesulfonate Salt). We followed its epifluorescence in a time-course manner (24 h to 7 weeks at regular intervals) using in vivo imaging. Our results show that the injected P-MSCs homed primarily to the visceral region in WNIN/GR-Ob (Ob-T2D) rats as compared to the WNIN/Control rats (Fig. 2a).

P-MSCs treatment clears peripheral blood glucose and restores insulin utilization in WNIN/GR-Ob (Ob-T2D) rats

To understand the beneficial effect of P-MSCs in clearing the peripheral blood glucose and restoration of insulin utilization in Ob-T2D conditions, we performed the ITT and GTT assays in WNIN/GR-Ob (Ob-T2D) rats, with and without P-MSCs injection, and compared it with the WNIN/Control rats. As shown previously²⁹, the WNIN/GR-Ob (Ob-T2D) rats show decreased glucose tolerance compared to the WNIN/Control rats (Fig. 2b). GTT and ITT assays using the peripheral blood indicate that treatment with P-MSCs improves the glucose utilization in WNIN/GR-Ob (Ob-T2D) rats compared to the WNIN/Control rats (Fig. 2b). Besides, we also observed that the WNIN/GR-Ob (Ob-T2D) rats, in response to P-MSCs injection, showed a significant increase in the serum insulin and C-peptide levels and a considerable decrease in the serum glucagon level (Fig. 2c). Further, we also observed decreased lipid peroxidation and reduced total cholesterol, total triglycerides, LDL, HDL, VLDL levels in the serum isolated from the WNIN/GR-Ob (Ob-T2D) rats in response to P-MSCs treatment (Supplementary Fig. 1a). “HOMA-IR” analysis is a widely accepted methodology for measuring IR and β-cell function³⁰. Using this approach, previously, it was shown that WNIN/GR-Ob (Ob-T2D) rats have nearly twofold higher IR, with a twofold reduction in β-cell function^24,25,29. Significantly, P-MSCs treatment reduced the IR in WNIN/GR-Ob (Ob-T2D) rats and enhanced the β-cell function to a level comparable to that of WNIN/Control rats (Fig. 2d,e). Our data confirm that de novo, P-MSCs injection increases insulin sensitivity and enhances glucose utilization in WNIN/GR-Ob (Ob-T2D) rats.

P-MSCs treatment restores the cytokine expression of the WNIN/GR-Ob (Ob-T2D) rats

Next, we addressed whether the P-MSCs injection also leads to cytokine remodeling. Using the dot blot assay, we analyzed both pro-and anti-inflammatory cytokine expression in the serum (Fig. 2f, Supplementary Fig. 2a) and in subcutaneous adipose (Fig. 3a, Supplementary Fig. 2b) and visceral adipose tissues (Fig. 3b, Supplementary Fig. 2c), from WNIN/Control and WNIN/GR-Ob (Ob-T2D) rats, with and without P-MSCs injection. WNIN/GR-Ob (Ob-T2D) rats showed an increased expression of pro-inflammatory cytokines IL-1α, IL-1β, IFN-γ, IL-6, MCP-1, MIP-3A, CINC-2, CINC-3, GM-CSF, and TNF-α in their serum and adipocyte milieu, when compared to the WNIN/Control rats (Figs. 2f, 3a,b; Supplementary Fig. 2a–c). Similarly, WNIN/GR-Ob (Ob-T2D) rats had a decreased expression of anti-inflammatory cytokines IL-10, IL-4, VEGF, β-NGF, Fractalkine, CNTF, LIX, and TIMP-1 in their adipocyte milieu and in their serum, when compared to the WNIN/Control rats (Figs. 2f, 3a,b; Supplementary Fig. 2a–c). Leptin is a well-established adipokine and regulates the food intake capacity^31,32. In addition to the alterations in the cytokine profile, we also observed that WNIN/GR-Ob (Ob-T2D) rats have decreased Leptin levels in their adipose milieu as well as in their serum when compared to the WNIN/Control rats (Figs. 2f, 3a,b; Supplementary Fig. 2a–c).

P-MSCs injection into the WNIN/Control rats had no significant impact on the cytokine expression levels (Figs. 2f,g, 3a–d; Supplementary Fig. 2a–c). Interestingly, we observed that P-MSCs injection to WNIN/GR-Ob (Ob-T2D) rats had restored the expression of both the pro-and anti-inflammatory cytokines, as well as Leptin expression, to the extent seen in the WNIN/Control rats (Figs. 2f,g, 3a,b; Supplementary Fig. 2a–c). We also reconfirmed the above observations that the P-MSCs injection restores cytokine profile in the WNIN/GR-Ob (Ob-T2D) rats, as shown by Multiplex-ELISA (Figs. 2g, 3c,d). Our qRT-PCR analysis gave a similar cytokine expression pattern at their respective mRNA levels, suggesting that the restoration of these cytokine alterations occurs at the transcriptional level (Supplementary Fig. 2a,b). These data confirm that P-MSCs injection re-establishes the normal cytokine profile in the WNIN/GR-Ob (Ob-T2D) rats.

P-MSCs treatment reduces the macrophage infiltration into adipose tissues of the WNIN/GR-Ob (Ob-T2D) rats

We next analyzed the extent of macrophage infiltration, since there was a reversal of cytokine expression with P-MSCs therapy in the WNIN/GR-Ob (Ob-T2D) rats. FACS and H&E analysis showed that both subcutaneous and visceral adipose tissues of the WNIN/GR-Ob (Ob-T2D) rats are enriched with CD11b+ macrophages compared to WNIN/Control WAT tissues (Fig. 3e,f, and Supplementary Fig. 3). P-MSCs injection had substantially lessened the macrophage infiltration by more than 1.4-fold in the WAT of WNIN/GR-Ob (Ob-T2D) rats (Fig. 3e,f).

P-MSCs treatment restores glucose homeostasis in the adipose tissues of WNIN/GR-Ob (Ob-T2D) rats

Next, we asked whether the injection of P-MSCs restores the glucose homeostasis in the adipose tissues of WNIN/GR-Ob (Ob-T2D) rats. For this, we first fractionated the SVF to enrich the immature and naïve adipocytes from mature subcutaneous and visceral adipocytes³³, and compared the respective glucose uptake capacity using 2-deoxy-2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-d-glucose (2-NBDG) assay, as explained in the materials and methods. SVF from the subcutaneous and visceral adipocytes of WNIN/GR-Ob (Ob-T2D) had less glucose uptake when compared to the SVF isolated from the subcutaneous and visceral adipocytes of WNIN/Control rats (Fig. 4a,b). Strikingly, a similar injection of P-MSCs had restored the glucose uptake capacity of the SVF from adipocytes isolated from the WNIN/GR-Ob (Ob-T2D) rats and was comparable with the WNIN/Control rats (Fig. 4a,b). However, we did not observe any significant change in the glucose uptake with or without P-MSCs injection (Fig. 4a,b) in WNIN/Control rats' adipocytes.

Hexokinase (HK) and Pyruvate kinase (PK) are the two rate-limiting enzymes involved in the glycolysis pathway³⁴, and their altered regulation has been well documented in Obesity and T2D³⁵. Here we show that P-MSCs injection was indeed functional and demonstrated an increase in HK and PK enzyme activity in the WNIN/GR-Ob (Ob-T2D) adipose tissues and was comparable with that of WNIN/Control rats (Fig. 4c,d).

To gain further insights into the metabolic flux, we next quantified the glycolytic pathway early intermediates using the LC–MS/MS analysis, both in the WNIN/Control and WNIN/GR-Ob (Ob-T2D) rats, with or without P-MSCs injection. The impetus from our earlier studies showed that WNIN/GR-Ob (Ob-T2D) rats show IR, associated with a lower glucose uptake capacity^24,25,29,36. In similar lines, WNIN/GR-Ob (Ob-T2D) rats showed reduced glycolytic early intermediates, both in subcutaneous and visceral adipose tissues, compared to the WNIN/Control rats (Fig. 4e,f). Treatment with P-MSCs to WNIN/GR-Ob (Ob-T2D) rats resulted in elevated key glycolytic early intermediates, i.e., Glucose-6-phosphate, Fructose-6-phosphate, and Fructose-1-6-bis phosphate (Fig. 4e,f). Note that there was two to threefold higher pyruvate levels in the WNIN/GR-Ob (Ob-T2D) rats' adipose tissues than the WNIN/Control rats (Fig. 4e,f). We did not observe any alteration in the pyruvate levels with the P-MSCs injection (Fig. 4e,f). All these results indicate the beneficial effects of P-MSCs therapy to restore the normal glucose uptake capacity of subcutaneous and visceral adipocytes in WNIN/GR-Ob (Ob-T2D) rats.

P-MSCs treatment upregulates the PI3K-Akt signaling in adipose tissues and restores the Glut4 expression in the WNIN/GR-Ob (Ob-T2D) rats

Since P-MSCs injection to the WNIN/GR-Ob (Ob-T2D) rats had reverted their glucose uptake and utilization, we next focused on understanding whether P-MSCs-mediated enhanced glucose uptake also utilizes the same pathway³⁷. Immunoblotting analysis showed that P-MSCs also upregulated the IRS-1 Ser612 phosphorylation and Akt Thr308 phosphorylation in both subcutaneous and visceral adipose tissues (Fig. 4g,h). In humans, PI3 kinase consists of a p100 catalytic subunit and a p85 regulatory subunit encoded by two isoforms, namely p85α and p85β³⁸. We observed that adipocytes from WNIN/GR-Ob (Ob-T2D) rats showed decreased steady-state expression levels of both the PI3K subunits (Fig. 4g,h). Interestingly, P-MSCs injection into WNIN/GR-Ob (Ob-T2D) rats effectively restored the protein expression of both p85α and p85β, comparable to WNIN/Control rats, both in subcutaneous and visceral adipocytes (Fig. 4g,h). More importantly, we observed that the P-MSCs treatment significantly upregulated the Glut4 protein expression in both the adipose depots in WNIN/GR-Ob (Ob-T2D) rats’ similar to WNIN/Control rats (Fig. 4g,h). These results indicate that enhanced PI3K-Akt signaling-mediated Glut4 upregulation with P-MSCs injection facilitates increased glucose uptake vis-à-vis insulin sensitivity, as well illustrated in adipose tissues WNIN/GR-Ob (Ob-T2D) rats.

P-MSCs enhance the glucose uptake by the adipocytes under the obesogenic milieu—an in vitro approach

To delineate the beneficial effects of P-MSCs treatment in the obesogenic milieu (Ob-T2D), we co-cultured P-MSCs with the adipocytes primed with and without high palmitate to induce obesogenic milieu. For this, we used 3T3L-1 cells, differentiated into adipocytes (with and without palmitate), and analyzed glucose uptake capacity by FACS analysis, using the 2-NBDG assay. Interestingly, we noted an enhanced uptake of glucose in adipocytes when co-cultured with the P-MSCs and in the presence of Insulin (Fig. 5a; compare the blue line with red line). The presence of high fat/obesogenic milieu had no significant impact on the glucose uptake capacity of adipocytes (Fig. 5a; compare blue with a green line), and insulin was also able to stimulate the glucose uptake under these conditions (Fig. 5a; compare blue with a green line). More importantly, P-MSCs co-culture had increased the glucose uptake capacity of these adipocytes in the obesogenic milieu (Fig. 5a; compare yellow with a green line). Note that this increased glucose uptake by the adipocytes is comparable to that of insulin stimulation. Since it is known that insulin stimulates glucose uptake via activating PI3K-Akt signaling, we presumed that P-MSCs also might be working through the same mechanism.

To elucidate the role of PI3K-Akt signaling in P-MSCs-induced glucose uptake by the adipocytes, we performed a similar assay as before, but in the presence of an Akt inhibitor. As expected, Akt inhibitor had decreased the insulin-stimulated glucose uptake capacity of adipocytes (Fig. 5a; compare red with brown line). More importantly, P-MSCs were unable to stimulate the adipocytes' glucose uptake capacity in the presence of AKT inhibitor (Fig. 5a; compare red with orange line). It is well known that PI3K- Akt signaling induces glucose uptake by glucose transporter 4 (Glut4) translocation into the membrane³⁹. Further, the increased glucose uptake by the adipocytes in the presence of P-MSCs is due to enhanced Glut4 expression by the adipocytes, as seen by the immunofluorescence analysis (Fig. 5b). All these data suggest that P-MSCs activate the PI3K-Akt pathway in the adipocytes, which in turn leads to their enhanced glucose uptake.

P-MSCs induce Glut4 surface translocation in adipocytes under obesogenic conditions in a PI3K-Akt-dependent mechanism

To confirm that P-MSCs indeed activate the PI3K-Akt signaling in adipocytes, we performed the immunoblot analysis under the same co-culture condition. Western blot analysis shows that insulin had stimulated the PI3K signaling, as demonstrated by Akt's increased phosphorylation and downstream targets, both in control and obesogenic conditions (Fig. 5c; compare lanes 1 with 2, and 3 with 4). Under the obesogenic conditions, P-MSCs co-culture had increased the Akt and its downstream signaling, similar to that of Insulin stimulation (Fig. 5c; compare lanes 5 with 3 and 4). Akt inhibitor had reduced the PI3K- Akt signaling activation induced by both Insulin (Fig. 5c; compare lane 10 with 9) and P-MSCs co-culture (Fig. 5c; compare lane 11 with 9). Irrespective of PI3K-Akt activation (either by insulin or by P-MSCs co-culture), we observed enhanced Glut4 surface translocation (Fig. 5c; compare lanes 1 with 2, 4, and 5 with 3). Akt inhibitor blocked the surface translocation of Glut4 (Fig. 5c; compare lanes 10, 11 with 9). Cytochalasin B is a well-known inhibitor for glucose transport⁴⁰. Both Insulin and P-MSCs co-culture were able to enhance the surface translocation of Glut4 in control, but not in the cytochalasin B pre-treated cells (Fig. 5c; compare lanes 7 and 8 with 6).

Discussion

The present study suggests for feasible application of P-MSCs therapy in the management of pre-clinical diabetes carried out in WNIN/GR-Ob (Ob-T2D) rats, which presents with Obesity, IGT, IR, and enhanced fat accumulation with age akin to human scenario^24,25. In addition to becoming pre-diabetic, these rats also show impaired pancreatic β-cell functions and increasing obesity with age^25,36. Interestingly, WAT accounts for 20 to 25 % of insulin-dependent glucose disposal in the body and plays a key role in maintaining glucose homeostasis⁴¹. In the present study, we have assessed glucose homeostasis, including insulin signaling, glucose sensitivity, and IR, in WATs before and after intramuscular injection of P-MSCs in WNIN/GR-Ob (Ob-T2D) rats. Our data reinstate the clinical efficacy of P-MSCs that intervened in WNIN/GR-Ob (Ob-T2D) rats to sensitize WAT to their endogenous insulin effectively, ameliorate glucose imbalance as well as normalize HOMA-IR, IGT, and ITT levels as compared to the Control rats (Fig. 2).

MSCs are one of the promising adult stem cells implicated in tissue repair⁴², and are well documented for their plasticity and differentiation potential into multiple cell types⁴³. Their immunomodulatory and potent anti-inflammatory effects to blunt pro-inflammatory responses find their increased application in several inflammatory diseases^26,27. P-MSCs have different secretory functions⁴⁴, wherein paracrine secretion plays a major role in the therapeutic effects of the MSCs on inflammation. Previous reports have shown that MSCs constitutively express cytokines such as interleukin, IL-6, -7, -8, -11, -12, -14, -15, -27, leukemia inhibitory factor, macrophage colony-stimulating factor, VEGF expression, and stem cell factor in addition to IL-10 and TGF- β at the mRNA level^26,27. Synergistic downregulation of pro-inflammatory cytokines and up-regulation of both pro-survival and anti-inflammatory factors advocate their therapeutic effects through autocrine and/or paracrine functions to modify the inflammatory environment⁴⁵. Also, P-MSCs have been reported safe for transplantation therapy compared to other adult stem cells, due to their limited antigenic response⁴⁶.

Multiple intramuscular injections (IM) of 1 × 10⁶ P-MSCs demonstrated more homing of fluorescent-labeled MSCs cells, predominant in the visceral region (Fig 2) of the adipose tissue of WNIN/GR-Ob (Ob-T2D) rats²⁴, which correlates with the systemic insult of visceral adipose tissue, reported during the obese conditions⁴⁷. MSCs mode of injection (intramuscular) into the thigh muscle also helps in the slow release of the paracrine secretion into the systemic circulation. The logic behind the intramuscular injection was to assess the cross-talk between the muscle and adipose tissues^48,49,50. Several studies^51,52,53 had shown that MSCs express multiple adhesion molecules and chemokine receptors, which aid in their migration towards various tissues in response to inflammation, and other major stimuli. In the present study, the adipose tissues exhibit a highly inflammatory microenvironment, wherein we postulate a similar migratory mechanism that could be suggestive of the homing pattern of the injected P-MSCs observed in the WNIN/GR-Ob (Ob-T2D) rats (Fig. 2a).

Among drug targets in treating obesity and allied complications, metformin appears most prominent and is the most common therapy, wherein it effectively sensitizes the muscle cells to Insulin^15,16. Metformin also enhances the AMPK-mediated Glut4 membrane translocation in pre-adipocytes⁵⁴. However, it has been shown that long-term metformin therapy exerts pro-inflammatory effects by inhibiting the NF-κB, through blocking of the PI3K-Akt pathway⁵⁵. Metformin also causes secondary complications, resulting in the neuronal, kidney, and gastric malfunction⁵⁶, paving the way for alternative therapies. Insulin stimulates the insulin receptor substrate-1 (IRS-1) phosphorylation, which leads to PI3K-Akt signaling activation³⁷. Akt activation also enhances the expression and cell surface translocation of the Glut4 receptor⁵⁷.

Interestingly, we have demonstrated that adipocytes isolated from subcutaneous and visceral adipose depots from WNIN/GR-Ob (Ob-T2D) rats had reduced Glut4 expression, probably underlining the low glucose uptake (Fig. 4). On the other hand, with P-MSCs therapy, we observed nearly a fourfold induction in the Glut4 expression in the WAT of WNIN/GR-Ob (Ob-T2D) rats, which correlates well with the enhanced glucose uptake of the SVF of WATs (Fig. 3). PI3K signaling is a central mechanism for performing key cellular functions, including proliferation, migration, and differentiation in addition to intracellular trafficking³⁷, well exemplified in several systems³⁷. We also observed that the P-MSCs therapy activated the PI3K-Akt signaling in the WATs (Fig. 4) and adipocytes (Fig. 5), suggesting the restoration of insulin signaling in these tissues (Fig. 4). Indeed, reduced Akt phosphorylation and its downstream effects due to inhibition of PI3K has been well documented in diabetes^37,58, obesity³⁷, as well as neurodegenerative diseases^37,58.

To gain further insights into the metabolic functions of P-MSCs under the obesogenic milieu (Ob-T2D rats), we assessed its effects on glucose metabolism, which is regulated and orchestrated by several metabolic pathways⁵⁸. It has also been reported that excess free fatty acids (FFAs) present in WAT under Ob-T2D conditions inhibit pyruvate dehydrogenase, impairing the muscle cells towards insulin-mediated glucose uptake and reducing glucose oxidation, which results in the accumulation of glycolytic metabolites in the muscle cells⁵⁹. In the present study, with P-MSCs injection, we demonstrated an increase in glycolytic influx (Fig. 4), which was evidenced by a quantitative increase in the formation of glycolytic intermediates studied in the WATs of WNIN/GR-Ob (Ob-T2D) rats as compared to the controls. Our findings have been in agreement with several other reports that show impaired glycolysis under diabetic conditions^34,60. Although P-MSCs therapy restored the early glycolytic intermediates in WNIN/GR-Ob (Ob-T2D) rats, pyruvate levels did not show any change with P-MSCs treatment and need to be explored further.

Inflammation is now accepted as a key factor in the pathology of T2D and possibly could be a key confounding player for β-cell death. Studies by Samuel et al.⁵⁹ on the NLRP3 inflammasome pathway as critical indicators contributing to impaired adipose tissue dysfunction and pancreatic β-cells underlining pre-clinical diabetes. The high levels of FFAs present in such conditions also activate the NF-κB pathway, both of which lead to pro-inflammatory cytokine production⁶¹. Besides, there will be a decrease in the expression of the anti-inflammatory cytokines in the adipose tissues⁶². Our present results corroborate with these findings (Figs. 2f, 3a,b) and show that obesity with T2D depicts a state of chronic low-grade inflammation to impact the normal β-cell functions and leads to β-cell exhaustion and cell death⁶³.

Cytokines play a crucial role in intracellular cell signaling and function in paracrine and endocrine signaling as immunomodulating agents, modifying the balance between humoral- and cell-mediated immunity^64,65. The cytokines are known to attract the macrophages into the surrounding milieu, causing inflammation and IR in obese people⁶⁶. Following published literature^64,65, MSCs of perinatal origin (P-MSCs) have shown to be more effective to blunt the inflammatory response in target tissues en route via paracrine secretions of MSCs and their cytokines/interleukin profiles (IL-6, -7, -8, -11, -12, -14, -15, -27, LIF, M-CSF)⁴². In addition to IL-10 and TGF-β1, which may play a crucial role in negating pro-inflammatory responses, and attenuate inflammatory milieu underlining non-communicable diseases (NCDs)⁶⁷. We also observed a baseline increase in the expression of pro-inflammatory cytokines in the WNIN/GR-Ob (Ob-T2D) rats, when compared to the control rats (Figs. 3 and 4); such as IL-6 (4.37-fold), IL-1β (4.125-fold), and TNF-α (2.55-fold) and a decreased expression of anti-inflammatory cytokines, such as IL-10 (ninefold), TGF-β (twofold), and IL-4 (eightfold).

Pro-inflammatory cytokines such as TNFα and IL6 are considered essential factors in developing obesity-associated IR⁶⁸. In adipocytes, the IL-6 signaling pathway, and an increase in the expression of TNFα, IL-1β are thought to inhibit insulin signaling by reducing the insulin-stimulated phosphorylation of IRS-1, protein kinase B (PKB/Akt), which causes an increase in the basal FFA accumulation, resulting in lipid accumulation and IR⁶⁹. Once these inflammatory signaling pathways are activated, they impair the insulin receptor and its mediated PI3K-PKB/Akt) activation of Glut4 translocation of glucose in adipose tissue.

MSCs therapy increases the surface Glut4 levels through activating the PI3K-Akt pathway⁷⁰. MSCs are also shown to decrease the hypertrophy of adipocytes. However, the underlying pathways are not yet known⁷¹. Our findings in WNIN/GR-Ob (Ob-T2D) rats are in similar lines with pre-clinical diabetic subjects presenting with Obesity/IR. and IGT to show a nearly fourfold increase in the IL-6 expression^72,73. IL-6 is generally derived from the SVF fraction of fat deposits, and its expression correlates directly to fat mass, i.e., with weight gain⁷⁴. We observed that P-MSCs injection effectively ameliorated the obesogenic milieu in WNIN/GR-Ob (Ob-T2D) rats and significantly reduced the expression of IL-6, TNF-α, and pro-inflammatory cytokines (Fig. 3c,d), and upregulated the expression of anti-inflammatory cytokines. Though the paracrine mechanism appears most probable to explain the beneficial effects of P-MSCs, still the factors secreted by the MSCs and their beneficial effects need to be understood in situ.

Nevertheless, we show for the cytokine remodeling evidenced from the present results (Figs. 2 and 3) to benefit the suppression of inflammatory milieu as well as lessen the macrophage infiltration in the WAT (Fig. 3) probably a synergistic effect of these cellular events could perhaps contribute for the normalization of adipose functions with P-MSCs administration, which otherwise shows a high degree of expression in obesity as well as in T2D⁷⁵. The anti-obesity effects of P-MSCs may be assigned to its paracrine and autocrine functions²⁸ that are released from their perivascular location under tissue insult or injury⁷⁶, or in modulating the niche and to activate the resident stem cells⁷⁷. In similar lines, the restoration of glucose homeostasis with P-MSCs intervention has been reported by Si et al. in diabetic model systems⁷⁰.

Stimulation and activation of inflammation in obesity are multifactorial⁷⁸. There is a need to study the role of glucotoxicity, FFAs, inflammasome stress kinases involved in obesity. This has been addressed in the present study by assessing the cross-talk between the high palmitate primed 3T3-L1 cells and co-culturing in vitro using a non-adherent system. We have tried to recapitulate the sequence of events to assess the glucose sensitivity and insulin signaling in-vitro to gain further insights into the beneficial effect of P-MSCs in the management of pre-clinical diabetes. We show that human placental MSCs co-cultured with 3T3-L1 cells induced PI3K-Akt pathway (Fig. 5) to increase insulin signaling protein phosphorylation, helping in glucose uptake and utilization.

Further, adipocytes (palmitate), when co-cultured with P-MSCs, show enhanced surface translocation of Glut4 into adipocytes (Fig. 5), which reconfirm our in vivo observations (Fig. 4). The addition of Glut4 inhibitor to the palmitate primed adipocytes inhibited this translocation, suggesting the specificity and regulation rendered by the P-MSCs towards glucose transportation⁴⁰. Further, our data provide insights to show that activation of the PI3K-Akt pathway is required for Glut4 translocation onto the adipocyte membrane. We here envisage that during co-culture, the secretome that contains several growth factors, cytokines may be responsible for eliciting the beneficial effects appreciable in our present system.

Taken together, this study highlights the beneficial effects of P-MSCs administered in vivo and in vitro (co-culture) and highlights the dynamics across multiple stress simultaneously. Using co-culture, we have identified the role of insulin-stimulated and P-MSCs stimulated phosphorylation events in glucose transport which complement metabolite-driven effects in the coordinated glucose metabolism regulation (Fig. 6). We envisage that future investigations will delineate the interplay between these MSCs in regulating metabolism.

Overall, our findings from both in vivo and in vitro work show the promise(s) and potent applications of P-MSCs to negate IR, ameliorate IGT in the WAT, enhance glucose sensitivity, and blunt inflammation by remodeling the cytokine profiles and IGT. Our findings open up newer avenues and approaches of P-MSCs to address the clinical management of NCDs, including lipodystrophy patients.

Materials and methods

Isolation, expansion, and characterization of human P-MSCs

The chorionic plate of the placenta was exposed by stripping off the amnion. This chorionic plate was then washed with phosphate buffer saline pH 7.2 (PBS) to remove traces of cord blood. This chorionic plate of the placenta was subjected to 0.25% trypsin–EDTA digestion for 30 min at 37 °C. Isolation was carried out as previously described^79,80. Their fibroblast morphology identified the human P-MSCs, and the cells were tested for viability, both Trypan Blue exclusion (TBE)³⁶. Their multipotent functions at passage three, i.e., their ability to differentiate into chondrogenic, osteogenic, and adipogenic lineages, were assessed as per published protocols²². Adipogenic differentiation was briefly evaluated by adipogenic induction medium and adipogenic maintenance medium (Merck Millipore SCR020, USA), and adipogenesis was confirmed using Oil Red O Staining. For chondrogenic and osteogenic differentiation, 1 × 10⁶ P-MSCs/cm² were plated onto tissue culture flasks, and chondrogenic, osteogenic lineages were induced by replacing the growth medium (DMEM/F12) with chondrogenic, osteogenic, differentiation bullet kit (C-28012, Sigma-Aldrich USA; SCR028, respectively, Merck Millipore, USA). Chondrogenesis was confirmed using Alcian Blue staining and osteogenesis by staining with Alizarin Red S. All the studies have been carried out using the third passage of P-MSCs, which has also been characterized for Stro-1 and CD133 cellular markers for P-MSCs.

Animal model and study design

We confirm that all methods were carried out in accordance with relevant guidelines and regulations for using animals. Also, we confirm that all the animal studies were carried out in compliance with the ARRIVE guidelines. Six-month-old WNIN/Control and WNIN/GR-Ob (Ob-T2D) Rats from the inbred strain from ICMR—National Institute of Nutrition (NIN) were used (n = 24) for the experiments. The rats were divided into four groups, WNIN/Control (n = 6), WNIN/Control injected with P-MSCs (n = 6), WNIN/GR-Ob (Ob-T2D) rats (n = 6), and WNIN/GR-Ob (Ob-T2D) rats injected with P-MSCs (n = 6). All the experiments were done in duplicates, i.e., Three sets of experiments using 6 rats per group were used in this study. Experimental protocols were approved by the Institutional Animal Ethical Committee (IAEC Committee, NCLAS, NIN (ICMR). The biochemical, cellular, and molecular studies were conducted at the end of 7 weeks after the 3rd P-MSCs injection unless specified. P-MSCs/1 × 10⁶ suspended uniformly in 100 µl of 1× phosphate-buffered saline (1× PBS) were injected intramuscular/thigh region of rats, one-shot/per week × 3. The control rats received an equivalent of 100 μl of 1× PBS.

P-MSCs tracking in vivo

Briefly, P-MSCs/third passage (1 × 10⁶) cells were stained with DiD, and homing of labeled cells was done similarly⁸¹. Briefly, the cells were incubated with DiD 10 µM (Life technologies, USA) for 1 h at 37 °C, using the manufacturer’s protocol, and suspended in 100 µl of 1× phosphate-buffered saline (1× PBS), and injected into the intramuscular/thigh region of rats, one-shot/per week × 3. In contrast, the controls received an equivalent amount of 1× PBS. At the end of 7 weeks of the experimental duration, the animals (3 animals/group) were measured for the longitudinal changes in fluorescent intensity at 640 nm (absorption) and 668 nm (excitation) every week post-injection using the IVIS Spectrum imaging system. The data were analyzed using Living Image software (PerkinElmer, USA).

Glucose and insulin tolerance test (GTT/ITT)

At the end of the 7th week, we performed ITT and GTT after fasting the animals for 8–10 h. For GTT, the rats were infused with a 20% glucose solution (2 g of glucose/kg of body mass), i.p⁸². For ITT, we followed method⁸³ of using the formula volume of IP glucose injection (μl) = 10 × body weight (g) and 0.75 IU of insulin/g body mass). The blood glucose levels were measured at 15, 30, 60, and 120 min after glucose and insulin injection. Glucose levels were measured using the ACCU-CHEK Advantage Meter (Roche Diagnostics GmbH, Mannheim, Germany).

Enzyme-linked immunosorbent assay

Serum Insulin, C-peptide, and Glucagon concentrations were measured using specific ELISA kits (Mercodia, Sweden). The homeostatic model assessment (HOMA) described as previously⁸⁴, was used to assess changes in IR (HOMA-IR) and pancreatic β-cell function (HOMA-β) in treated groups during the experimental period. The following equations were used to calculate the HOMA-IR index and HOMA-β index (HBCI): HOMA-IR index = (FBG [mmol/L] × FINS [units/L])/22.5) and HOMA-β = (20 × FINS [units/L])/(FBG [mmol/L] − 3.5).

Measurement of serum and tissue cytokines (Dot Blot)

Serum and tissue cytokine profiling was performed according to the manufacture's protocol (Abcam, USA). Briefly, the tissue lysates and serum were incubated at 4 °C with the membrane overnight and washed with wash buffer I and II three times (5 min each) and the biotin-conjugated cytokines (CINC-2, CINC-3, CNTF, Fractalkine, GM-CSF, IFN-γ, IL-1α, IL-1β, IL-4, IL-6, IL-10, Leptin, LIX, MCP-1, MIP-3α, β-NGF, TIMP-1, TNF-α, VEGF) were incubated with a membrane overnight at 4 °C then washed wash buffer I and II for three times (5 min each), incubated with HRP-conjugated Streptavidin into each well and incubated for 2 h at RT, washed three times (5 min each) again, with wash buffer I and II before imaging with the ChemiDoc.

Measurement of serum and tissue cytokine levels

The following major pro-and anti-inflammatory cytokines from serum and tissue lysates (visceral and subcutaneous) were analyzed: TNF-α, Monocyte Chemotactic Protein 1 (MCP-1; systemic name CCL2), IL-6, GM-CSF, IL-18, IFN-γ, Leptin, and VEGF were measured using multiplex map (Millipore, USA). IL-1β, IL-10, IL-12 p70, IL-13, IL-4, IP-10, TNFα, and TGF-β were analyzed by ELISA using the Procaratplex multiplex kit (Invitrogen, USA). All the multiplexing assays were performed as per the manufacturer's instructions.

CD11b study by flow cytometer

Adipocytes have been isolated according to the previous protocols. Adipose tissue was subjected to collagenase type I digestion for 1h at room temperature, passed through a 100 µ filtration sieve and spun at 1200 rpm for 5 min, and collected the SVF⁸⁵. SVF was then treated with CD11b (Life Technologies, USA) at 10 µm/ml concentration for 35 min and washed with PBS, and analyzed further using a flow cytometer.

Real-time quantitative PCR (cytokines markers)

The qRT-PCR analysis was performed as described previously⁸⁶, with the following modifications. Total RNA was extracted using the Trizol reagent (DSS-Takara Biosciences, India), and cDNA synthesis was performed using the enhanced Avian Reverse Transcriptase (Sigma-Aldrich, USA) according to the manufacturer's instructions. The gene expression was analyzed using the 7500 Fast Real-Time PCR instrument (Applied Biosystems, Foster City, CA, USA). β-actin expression was used as the reference gene. The list of primers used for amplification is given in Supplementary Table-1 (qRT-PCR).

Glucose transport assay

Glucose transport was assessed in the SVF using glucose analogue, 2-NBDG, as described previously³⁹. At the end of 7 weeks, visceral and subcutaneous adipose tissues were dissected under sterile conditions and allowed to recover and processed in Krebs–Ringer HEPES (KRH) buffer containing 11.1 mM glucose for 1 h. After the initial recovery, the fat deposits were pre-treated with or without human recombinant insulin (100 nM) for 20 min in a shaking water bath. The isolation of SVFs was carried out using collagenase (type IV) digestion³⁹ in the KRH buffer. After repeated washings in DMEM/F12 medium without glucose and filtration, the cells were diluted 5× times with Krebs–Ringer Phosphate (KRP) buffer pH 7.4, supplemented with 0.2% (w/v) BSA. Following this, 2-NBDG (0.5 mM) was added and incubated for 30 min at 37 °C in a shaking water bath. The cells were washed three times in ice-cold 1× PBS and kept on ice to prevent further insulin-stimulated membrane trafficking. 2-NBDG uptake was performed on ice to ensure that the uptake rate was solely dependent on the membrane trafficking that had occurred during the preceding period of insulin stimulation. A control sample, which lacks the 2-NBDG, was used to set the flow cytometer compensation and gate parameters. Each experiment was performed in duplicates, and the average was considered as one biological replicate.

Glycolysis enzyme activity assays

The Hexokinase assay was performed as previously described⁸⁷. Briefly, 20 µg of fresh tissue lysate was added to 1 ml of reaction buffer for hexokinase (50 mM Tris HCl (Sigma-Aldrich), pH 7.5, 10 mM MgCl₂ (Sigma-Aldrich), 0.6 mM ATP (Sigma-Aldrich), 100 mM glucose (Sigma-Aldrich), 0.2 mM NADP+ (Sigma-Aldrich), and 0.1 units of glucose-6-phosphate dehydrogenase (Sigma-Aldrich)). Ten units of glyceraldehyde-3-phosphate dehydrogenase (Sigma-Aldrich) per ml was used for analyzing the Hexokinase activity. The Pyruvate kinase assay was performed as previously described⁸⁷. Briefly, 20 µg of fresh tissue lysate was added to 1 ml of reaction buffer for pyruvate kinase (50 mM Tris HCl (Sigma-Aldrich), pH 7.5, 5 mM MgCl₂ (Sigma-Aldrich), 5 mM ATP (Sigma-Aldrich), 0.2 mM NADH (Sigma-Aldrich) 100 mM KCl (Sigma-Aldrich), 5 mM Na₂HPO₄ (Sigma-Aldrich), 5 mM MgCl₂ (Sigma-Aldrich), 0.01 mM AMP (Sigma-Aldrich)) 5 mM fructose-6-phosphate (Sigma-Aldrich), 5 units of triosephosphate isomerase (Sigma-Aldrich) per ml, 1 unit of aldolase (Sigma-Aldrich) per ml was added to check the pyruvate kinase activity. A negative and positive control has been included without tissue lysate and with 0.05 units of hexokinase and pyruvate kinase in both the assays. Enzyme activities were measured and represented as the change in absorbance/min, calculated using a linear portion of the obtained curve.

Metabolomic analysis by LC–MS

Subcutaneous and Visceral adipose tissues were processed for metabolite analysis^40,88. The samples were quickly snap-frozen with liquid nitrogen and incubated in – 80 °C for 10 min. The tissues were quickly ground and blended in a mortar. Powdered fat tissues (20 mg) were then placed into a 1.5 mL scaled Eppendorf tube containing 300 μl lysis buffer (9:1 methanol: chloroform), mixed with 500 μL water. The samples were immediately vortexed for 3 min, and the tissues were subjected to centrifugation at 16,000×g for 5 min at 4 °C to remove the cell debris. The supernatant was stored at − 80 °C, before proceeding for LC–MS/MS analysis. Glucose-1-Phosphate, Glucose-6-Phosphate, Fructose-1-Phosphate, Fructose-1,6-bisphosphate, Pyruvate, Phosphoenolpyruvate, and the standards were purchased from Sigma-Aldrich, USA. Chloramphenicol (internal standard) (Sigma-Aldrich, USA) was prepared and diluted to 100 ng/mL using methanol.

Cell line and growth conditions

3T3-L1 fibroblasts were maintained as described previously⁴⁰. Differentiation was induced at 100% confluence by adding 250 nM dexamethasone, 350 nM insulin, and 0.5 mM 3-isobutyl-1-methylxanthine for 72 h. At the end of time points, the cells were incubated in media containing 350 nM insulin for a further 72 h. The adipocytes were used between days 9 and 12 after initiation of differentiation for all the assays. For co-culturing, the 3T3-L1 were seeded in the lower chamber of trans-well plates and treated with TNF-α (10 ng/ml), IL-1β (10 ng/ml), IL-6 (10 ng/ml), and Palmitic acid (0.5 mM) and glucose (35 mM), after serum starvation for 48 h. At the end of 48 h, human P-MSCs were plated on the upper chamber of the trans-well plate using the same medium and co-cultured. The samples were collected 24 h after co-culturing and processed further. Akt inhibitor 1/2 was purchased from TCI Chemicals and used at 30 µM final concentration.

Glucose transport assay

Glucose transport was assessed using glucose analogue, 2-NBDG, as previously described³⁹, with the following modifications. 100 nM insulin was added for specified times, and to determine non-specific glucose uptake, 25 μM cytochalasin B was added 5 min before the addition of 2-deoxyglucose. A control sample lacking 2-NBDG was used to set the flow cytometer compensation and gate parameters for 2-NBDG positive and negative events.

Immunofluorescence

Immunofluorescence experiments were carried out as described by us previously³⁶. The cells were incubated with Glut4 primary antibody at 4 °C overnight. The following secondary antibody was used for visualization: goat anti-rabbit antibody conjugated with Cy3. The nuclei were counterstained with DAPI.

Western blotting analysis (insulin signaling pathway)

Subcutaneous and visceral adipose tissue were processed for Western blotting^40,89. The tissues were homogenized as described previously⁹⁰, in 1×RIPA buffer containing 150 mM sodium chloride, 1% Nonidet P-40, 0.5% Sodium deoxycholate, 0.1% SDS (sodium dodecyl sulfate), 50 mM Tris (pH 8.0) and protease inhibitor (Pierce). Proteins were separated by SDS-PAGE, immunoblotted with indicated antibodies, and imaged by ChemiDoc. The tissue lysates (40 μg protein/lane) were briefly resolved by SDS-PAGE and transferred to PVDF membranes. Membranes were blocked for at least 1 h with 4% (w/v) skim milk powder in Tris-buffered saline with 0.1% Tween 20 (TBST). The membranes were incubated overnight at 4 °C with the following primary antibodies: anti-β-actin (1:1000, mouse monoclonal, pierce), anti-PI3K-α (1:1000, rabbit polyclonal, CST), anti- PI3K-β (1:1000, rabbit polyclonal, CST), anti-PI3K-γ (1:1000, rabbit polyclonal, CST), anti-AKT (1:1000, mouse monoclonal, CST), anti-P-Ser 473 AKT (1:1000, mouse monoclonal, CST), anti-P-Thr 308 AKT (1:1000, mouse monoclonal CST), anti-IRS-1 (1:1000, mouse monoclonal, CST), anti-P-Ser 307 IRS1 (1:1000, mouse monoclonal, CST), anti-Glut4 (1:1000, mouse monoclonal, CST), anti-P-c-Raf ser 259 (1:1000, mouse monoclonal, CST), anti-P-PTEN (1:1000, mouse monoclonal, CST), anti-P-PDK1 (1:1000, mouse monoclonal, CST), anti-mTOR (1:1000, rabbit polyclonal, CST) and anti-P-GSK3β (1:1000, mouse monoclonal, anti-IRS-1 (1:1000, mouse monoclonal, CST). Membranes were then washed three times, for 15 min with TBST, incubated for 1 h at room temperature with the respective secondary antibodies diluted 1/10,000 in 5% (w/v) skim milk powder in TBST. The membranes were rewashed three times, 15 min each with TBST, before imaging with the ChemiDoc using G-Box from Syngene international limited. All the gels/blots used in the pictures are in compliance with the digital image and integrity policies.

Statistical analysis

The results represent the mean of 6 rats per group. The “p” values were calculated using the Two-way ANOVA for normally distributed data and the multiple comparison test. Statistical analysis was done using GraphPad Prism (Ver 8.0). Heatmaps were plotted using GraphPadprsim.

Ethics approval

Institutional Animal Ethics Committees (IAECs): P35F/IAEC/NIN/11/2012/VV/WNIN. Institutional Human Ethics Committees: MHB/SCR/021.

Change history

28 September 2021
A Correction to this paper has been published: https://doi.org/10.1038/s41598-021-99380-z

References

Polsky, S. & Ellis, S. L. Obesity, insulin resistance, and type 1 diabetes mellitus. Curr. Opin. Endocrinol. Diabetes Obes. 22, 277–282. https://doi.org/10.1097/med.0000000000000170 (2015).
Article CAS PubMed Google Scholar
Saltiel, A. R. & Olefsky, J. M. Inflammatory mechanisms linking obesity and metabolic disease. J. Clin. Investig. 127, 1–4. https://doi.org/10.1172/jci92035 (2017).
Article PubMed PubMed Central Google Scholar
Hruby, A. & Hu, F. B. The epidemiology of obesity: A big picture. Pharmacoeconomics 33, 673–689. https://doi.org/10.1007/s40273-014-0243-x (2015).
Article PubMed PubMed Central Google Scholar
Leitner, D. R. et al. Obesity and type 2 diabetes: Two diseases with a need for combined treatment strategies—EASO can lead the way. Obes. Facts 10, 483–492. https://doi.org/10.1159/000480525 (2017).
Article PubMed PubMed Central Google Scholar
Stafeev, I. S., Vorotnikov, A. V., Ratner, E. I., Menshikov, M. Y. & Parfyonova, Y. V. Latent inflammation and insulin resistance in adipose tissue. Int. J. Endocrinol. 2017, 5076732. https://doi.org/10.1155/2017/5076732 (2017).
Article CAS PubMed PubMed Central Google Scholar
Feng, J. et al. The role of JNk signaling pathway in obesity-driven insulin resistance. Diabetes Metab. Syndr. Obes. Targets Ther. 13, 1399–1406. https://doi.org/10.2147/dmso.S236127 (2020).
Article CAS Google Scholar
Samuel, V. T., Petersen, K. F. & Shulman, G. I. Lipid-induced insulin resistance: Unravelling the mechanism. Lancet 375, 2267–2277. https://doi.org/10.1016/s0140-6736(10)60408-4 (2010).
Article CAS PubMed PubMed Central Google Scholar
Hardy, O. T., Czech, M. P. & Corvera, S. What causes the insulin resistance underlying obesity?. Curr. Opin. Endocrinol. Diabetes Obes. 19, 81–87. https://doi.org/10.1097/MED.0b013e3283514e13 (2012).
Article CAS PubMed PubMed Central Google Scholar
Boden, G. & Laakso, M. Lipids and glucose in type 2 diabetes: What is the cause and effect?. Diabetes Care 27, 2253–2259. https://doi.org/10.2337/diacare.27.9.2253 (2004).
Article CAS PubMed Google Scholar
Choe, S. S., Huh, J. Y., Hwang, I. J., Kim, J. I. & Kim, J. B. Adipose tissue remodeling: Its role in energy metabolism and metabolic disorders. Front. Endocrinol. 7, 30. https://doi.org/10.3389/fendo.2016.00030 (2016).
Article Google Scholar
Surmi, B. K. & Hasty, A. H. Macrophage infiltration into adipose tissue: Initiation, propagation and remodeling. Futur. Lipidol. 3, 545–556. https://doi.org/10.2217/17460875.3.5.545 (2008).
Article CAS Google Scholar
Arango Duque, G. & Descoteaux, A. Macrophage cytokines: Involvement in immunity and infectious diseases. Front. Immunol. 5, 491. https://doi.org/10.3389/fimmu.2014.00491 (2014).
Article CAS PubMed PubMed Central Google Scholar
Rena, G., Hardie, D. G. & Pearson, E. R. The mechanisms of action of metformin. Diabetologia 60, 1577–1585. https://doi.org/10.1007/s00125-017-4342-z (2017).
Article CAS PubMed PubMed Central Google Scholar
Hundal, R. S. et al. Mechanism by which metformin reduces glucose production in type 2 diabetes. Diabetes 49, 2063–2069. https://doi.org/10.2337/diabetes.49.12.2063 (2000).
Article CAS PubMed Google Scholar
Musi, N. et al. Metformin increases AMP-activated protein kinase activity in skeletal muscle of subjects with type 2 diabetes. Diabetes 51, 2074–2081. https://doi.org/10.2337/diabetes.51.7.2074 (2002).
Article CAS PubMed Google Scholar
Wang, J. et al. Metformin ameliorates skeletal muscle insulin resistance by inhibiting miR-21 expression in a high-fat dietary rat model. Oncotarget 8, 98029–98039. https://doi.org/10.18632/oncotarget.20442 (2017).
Article PubMed PubMed Central Google Scholar
Levri, K. M. et al. Metformin as treatment for overweight and obese adults: A systematic review. Ann. Fam. Med. 3, 457–461. https://doi.org/10.1370/afm.343 (2005).
Article PubMed PubMed Central Google Scholar
Luo, T. et al. AMPK activation by metformin suppresses abnormal extracellular matrix remodeling in adipose tissue and ameliorates insulin resistance in obesity. Diabetes 65, 2295–2310. https://doi.org/10.2337/db15-1122 (2016).
Article CAS PubMed PubMed Central Google Scholar
Chaudhury, A. et al. Clinical review of antidiabetic drugs: Implications for type 2 diabetes mellitus management. Front. Endocrinol. 8, 6. https://doi.org/10.3389/fendo.2017.00006 (2017).
Article Google Scholar
Deacon, C. F. & Lebovitz, H. E. Comparative review of dipeptidyl peptidase-4 inhibitors and sulphonylureas. Diabetes Obes. Metab. 18, 333–347. https://doi.org/10.1111/dom.12610 (2016).
Article CAS PubMed Google Scholar
Jiang, R. et al. Transplantation of placenta-derived mesenchymal stem cells in type 2 diabetes: A pilot study. Front. Med. 5, 94–100. https://doi.org/10.1007/s11684-011-0116-z (2011).
Article PubMed Google Scholar
Kadam, S., Muthyala, S., Nair, P. & Bhonde, R. Human placenta-derived mesenchymal stem cells and islet-like cell clusters generated from these cells as a novel source for stem cell therapy in diabetes. The review of diabetic studies. RDS 7, 168–182. https://doi.org/10.1900/rds.2010.7.168 (2010).
Article PubMed PubMed Central Google Scholar
Lee, R. H. et al. Multipotent stromal cells from human marrow home to and promote repair of pancreatic islets and renal glomeruli in diabetic NOD/scid mice. Proc. Natl. Acad. Sci. USA. 103, 17438–17443. https://doi.org/10.1073/pnas.0608249103 (2006).
Article ADS CAS PubMed PubMed Central Google Scholar
Harishankar, N., Vajreswari, A. & Giridharan, N. V. WNIN/GR-Ob—an insulin-resistant obese rat model from inbred WNIN strain. Indian J. Med. Res. 134, 320–329 (2011).
CAS PubMed PubMed Central Google Scholar
Venkatesan, V. et al. Obesity, insulin resistance, and metabolic syndrome: A study in WNIN/Ob rats from a pancreatic perspective. Biomed. Res. Int. 2013, 617569. https://doi.org/10.1155/2013/617569 (2013).
Article PubMed PubMed Central Google Scholar
Liu, Y. et al. Effects of inflammatory factors on mesenchymal stem cells and their role in the promotion of tumor angiogenesis in colon cancer. J. Biol. Chem. 286, 25007–25015. https://doi.org/10.1074/jbc.M110.213108 (2011).
Article CAS PubMed PubMed Central Google Scholar
Gao, F. et al. Mesenchymal stem cells and immunomodulation: Current status and future prospects. Cell Death Dis. 7, e2062. https://doi.org/10.1038/cddis.2015.327 (2016).
Article CAS PubMed PubMed Central Google Scholar
Kamal, M. M. & Kassem, D. H. Therapeutic potential of Wharton’s jelly mesenchymal stem cells for diabetes: Achievements and challenges. Front. Cell Dev. Biol. 8, 16. https://doi.org/10.3389/fcell.2020.00016 (2020).
Article PubMed PubMed Central Google Scholar
Singh, H. et al. Islet adaptation to obesity and insulin resistance in WNIN/GR-Ob rats. Islets 6, e998099. https://doi.org/10.1080/19382014.2014.998099 (2014).
Article PubMed Google Scholar
Wallace, T. M., Levy, J. C. & Matthews, D. R. Use and abuse of HOMA modeling. Diabetes Care 27, 1487–1495. https://doi.org/10.2337/diacare.27.6.1487 (2004).
Article PubMed Google Scholar
Ahima, R. S. Revisiting leptin’s role in obesity and weight loss. J. Clin. Investig. 118, 2380–2383. https://doi.org/10.1172/jci36284 (2008).
Article CAS PubMed PubMed Central Google Scholar
Ryan, D. H. et al. Nonsurgical weight loss for extreme obesity in primary care settings: Results of the Louisiana Obese Subjects Study. Arch. Intern. Med. 170, 146–154. https://doi.org/10.1001/archinternmed.2009.508 (2010).
Article CAS PubMed Google Scholar
Bora, P. & Majumdar, A. S. Adipose tissue-derived stromal vascular fraction in regenerative medicine: A brief review on biology and translation. Stem Cell Res. Ther. 8, 145. https://doi.org/10.1186/s13287-017-0598-y (2017).
Article CAS PubMed PubMed Central Google Scholar
Vijayalakshmi, R. & Bamji, M. S. Altered glucose metabolism in female rats treated with sex steroids: Reversal by excess pyridoxine. Indian J. Biochem. Biophys. 24, 329–335 (1987).
CAS PubMed Google Scholar
Tanner, L. B. et al. Four key steps control glycolytic flux in mammalian cells. Cell Syst. 7, 49-62.e48. https://doi.org/10.1016/j.cels.2018.06.003 (2018).
Article CAS PubMed PubMed Central Google Scholar
Madhira, S. L. et al. Promise(s) of mesenchymal stem cells as an in vitro model system to depict pre-diabetic/diabetic milieu in WNIN/GR-Ob mutant rats. PLoS ONE 7, e48061. https://doi.org/10.1371/journal.pone.0048061 (2012).
Article ADS CAS PubMed PubMed Central Google Scholar
Fruman, D. A. et al. The PI3K pathway in human disease. Cell 170, 605–635. https://doi.org/10.1016/j.cell.2017.07.029 (2017).
Article CAS PubMed PubMed Central Google Scholar
Hakuno, F. & Takahashi, S. I. IGF1 receptor signaling pathways. J. Mol. Endocrinol. 61, T69-t86. https://doi.org/10.1530/jme-17-0311 (2018).
Article CAS PubMed Google Scholar
Liu, Y. et al. Protein inhibitor of activated STAT 1 (PIAS1) protects against obesity-induced insulin resistance by inhibiting inflammation cascade in adipose tissue. Diabetes 64, 4061–4074. https://doi.org/10.2337/db15-0278 (2015).
Article CAS PubMed Google Scholar
Krycer, J. R. et al. Dynamic metabolomics reveals that insulin primes the adipocyte for glucose metabolism. Cell Rep. 21, 3536–3547. https://doi.org/10.1016/j.celrep.2017.11.085 (2017).
Article CAS PubMed Google Scholar
Jani, R. et al. Decreased non-insulin-dependent glucose clearance contributes to the rise in fasting plasma glucose in the nondiabetic range. Diabetes Care 31, 311–315. https://doi.org/10.2337/dc07-1593 (2008).
Article CAS PubMed Google Scholar
Pittenger, M. F. et al. Mesenchymal stem cell perspective: Cell biology to clinical progress. NPJ Regener. Med. 4, 22. https://doi.org/10.1038/s41536-019-0083-6 (2019).
Article CAS Google Scholar
Lv, F. J., Tuan, R. S., Cheung, K. M. & Leung, V. Y. Concise review: The surface markers and identity of human mesenchymal stem cells. Stem Cells 32, 1408–1419. https://doi.org/10.1002/stem.1681 (2014).
Article CAS PubMed Google Scholar
Scheel, C. et al. Paracrine and autocrine signals induce and maintain mesenchymal and stem cell states in the breast. Cell 145, 926–940. https://doi.org/10.1016/j.cell.2011.04.029 (2011).
Article CAS PubMed PubMed Central Google Scholar
Mastri, M., Lin, H. & Lee, T. Enhancing the efficacy of mesenchymal stem cell therapy. World J. Stem Cells 6, 82–93. https://doi.org/10.4252/wjsc.v6.i2.82 (2014).
Article PubMed PubMed Central Google Scholar
Musiał-Wysocka, A., Kot, M. & Majka, M. The pros and cons of mesenchymal stem cell-based therapies. Cell Transplant. 28, 801–812. https://doi.org/10.1177/0963689719837897 (2019).
Article PubMed PubMed Central Google Scholar
Godisela, K. K. et al. Impact of obesity with impaired glucose tolerance on retinal degeneration in a rat model of metabolic syndrome. Mol. Vis. 23, 263–274 (2017).
CAS PubMed PubMed Central Google Scholar
Sarr, O. et al. Subcutaneous and visceral adipose tissue secretions from extremely obese men and women both acutely suppress muscle insulin signaling. Int. J. Mol. Sci. https://doi.org/10.3390/ijms18050959 (2017).
Article PubMed PubMed Central Google Scholar
Argilés, J. M., López-Soriano, J., Almendro, V., Busquets, S. & López-Soriano, F. J. Cross-talk between skeletal muscle and adipose tissue: A link with obesity?. Med. Res. Rev. 25, 49–65. https://doi.org/10.1002/med.20010 (2005).
Article PubMed Google Scholar
Stanford, K. I. & Goodyear, L. J. Muscle-adipose tissue cross talk. Cold Spring Harb. Perspect. Med. https://doi.org/10.1101/cshperspect.a029801 (2018).
Article PubMed PubMed Central Google Scholar
Baek, S. J., Kang, S. K. & Ra, J. C. In vitro migration capacity of human adipose tissue-derived mesenchymal stem cells reflects their expression of receptors for chemokines and growth factors. Exp. Mol. Med. 43, 596–603. https://doi.org/10.3858/emm.2011.43.10.069 (2011).
Article CAS PubMed PubMed Central Google Scholar
Vallés, G. et al. Influence of inflammatory conditions provided by macrophages on osteogenic ability of mesenchymal stem cells. Stem Cell Res. Ther. 11, 57. https://doi.org/10.1186/s13287-020-1578-1 (2020).
Article CAS PubMed PubMed Central Google Scholar
Shree, N., Venkategowda, S., Venkatranganna, M. V., Datta, I. & Bhonde, R. R. Human adipose tissue mesenchymal stem cells as a novel treatment modality for correcting obesity induced metabolic dysregulation. Int. J. Obes. 2005(43), 2107–2118. https://doi.org/10.1038/s41366-019-0438-5 (2019).
Article CAS Google Scholar
Lee, J. O. et al. Metformin regulates glucose transporter 4 (GLUT4) translocation through AMP-activated protein kinase (AMPK)-mediated Cbl/CAP signaling in 3T3-L1 preadipocyte cells. J. Biol. Chem. 287, 44121–44129. https://doi.org/10.1074/jbc.M112.361386 (2012).
Article CAS PubMed PubMed Central Google Scholar
Isoda, K. et al. Metformin inhibits proinflammatory responses and nuclear factor-kappaB in human vascular wall cells. Arterioscler. Thromb. Vasc. Biol. 26, 611–617. https://doi.org/10.1161/01.Atv.0000201938.78044.75 (2006).
Article CAS PubMed Google Scholar
Nasri, H. & Rafieian-Kopaei, M. Metformin: Current knowledge. J. Res. Med. Sci. 19, 658–664 (2014).
PubMed PubMed Central Google Scholar
Beg, M., Abdullah, N., Thowfeik, F. S., Altorki, N. K. & McGraw, T. E. Distinct Akt phosphorylation states are required for insulin regulated Glut4 and Glut1-mediated glucose uptake. Elife https://doi.org/10.7554/eLife.26896 (2017).
Article PubMed PubMed Central Google Scholar
Czech, M. P. Insulin action and resistance in obesity and type 2 diabetes. Nat. Med. 23, 804–814. https://doi.org/10.1038/nm.4350 (2017).
Article CAS PubMed PubMed Central Google Scholar
Samuel, V. T. & Shulman, G. I. Mechanisms for insulin resistance: Common threads and missing links. Cell 148, 852–871. https://doi.org/10.1016/j.cell.2012.02.017 (2012).
Article CAS PubMed PubMed Central Google Scholar
Rabbani, N. & Thornalley, P. J. Hexokinase-2 glycolytic overload in diabetes and ischemia-reperfusion injury. Trends Endocrinol. Metab. 30, 419–431. https://doi.org/10.1016/j.tem.2019.04.011 (2019).
Article CAS PubMed Google Scholar
Donath, M. Y., Dalmas, É., Sauter, N. S. & Böni-Schnetzler, M. Inflammation in obesity and diabetes: Islet dysfunction and therapeutic opportunity. Cell Metab. 17, 860–872. https://doi.org/10.1016/j.cmet.2013.05.001 (2013).
Article CAS PubMed Google Scholar
Pirola, L. & Ferraz, J. C. Role of pro- and anti-inflammatory phenomena in the physiopathology of type 2 diabetes and obesity. World J. Biol. Chem. 8, 120–128. https://doi.org/10.4331/wjbc.v8.i2.120 (2017).
Article PubMed PubMed Central Google Scholar
Usmani-Brown, S. et al. β cell responses to inflammation. Mol. Metab. 27s, S104–S113. https://doi.org/10.1016/j.molmet.2019.06.013 (2019).
Article CAS PubMed Google Scholar
Asghar, A. & Sheikh, N. Role of immune cells in obesity induced low grade inflammation and insulin resistance. Cell. Immunol. 315, 18–26. https://doi.org/10.1016/j.cellimm.2017.03.001 (2017).
Article CAS PubMed Google Scholar
Fève, B. & Bastard, J. P. The role of interleukins in insulin resistance and type 2 diabetes mellitus. Nat. Rev. Endocrinol. 5, 305–311. https://doi.org/10.1038/nrendo.2009.62 (2009).
Article CAS PubMed Google Scholar
Sell, H., Habich, C. & Eckel, J. Adaptive immunity in obesity and insulin resistance. Nat. Rev. Endocrinol. 8, 709–716. https://doi.org/10.1038/nrendo.2012.114 (2012).
Article CAS PubMed Google Scholar
Taylor, A., Verhagen, J., Blaser, K., Akdis, M. & Akdis, C. A. Mechanisms of immune suppression by interleukin-10 and transforming growth factor-beta: The role of T regulatory cells. Immunology 117, 433–442. https://doi.org/10.1111/j.1365-2567.2006.02321.x (2006).
Article CAS PubMed PubMed Central Google Scholar
Kern, L. et al. Obesity-induced TNFα and IL-6 signaling: The missing link between obesity and inflammation-driven liver and colorectal cancers. Cancers https://doi.org/10.3390/cancers11010024 (2018).
Article PubMed PubMed Central Google Scholar
Rotter, V., Nagaev, I. & Smith, U. Interleukin-6 (IL-6) induces insulin resistance in 3T3-L1 adipocytes and is, like IL-8 and tumor necrosis factor-alpha, overexpressed in human fat cells from insulin-resistant subjects. J. Biol. Chem. 278, 45777–45784. https://doi.org/10.1074/jbc.M301977200 (2003).
Article CAS PubMed Google Scholar
Si, Y. et al. Infusion of mesenchymal stem cells ameliorates hyperglycemia in type 2 diabetic rats: Identification of a novel role in improving insulin sensitivity. Diabetes 61, 1616–1625. https://doi.org/10.2337/db11-1141 (2012).
Article CAS PubMed PubMed Central Google Scholar
Wang, M., Song, L., Strange, C., Dong, X. & Wang, H. Therapeutic effects of adipose stem cells from diabetic mice for the treatment of type 2 diabetes. Mol. Ther. 26, 1921–1930. https://doi.org/10.1016/j.ymthe.2018.06.013 (2018).
Article CAS PubMed PubMed Central Google Scholar
Fain, J. N., Madan, A. K., Hiler, M. L., Cheema, P. & Bahouth, S. W. Comparison of the release of adipokines by adipose tissue, adipose tissue matrix, and adipocytes from visceral and subcutaneous abdominal adipose tissues of obese humans. Endocrinology 145, 2273–2282. https://doi.org/10.1210/en.2003-1336 (2004).
Article CAS PubMed Google Scholar
Fried, S. K., Bunkin, D. A. & Greenberg, A. S. Omental and subcutaneous adipose tissues of obese subjects release interleukin-6: Depot difference and regulation by glucocorticoid. J. Clin. Endocrinol. Metab. 83, 847–850. https://doi.org/10.1210/jcem.83.3.4660 (1998).
Article CAS PubMed Google Scholar
Bastard, J. P. et al. Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss. J. Clin. Endocrinol. Metab. 85, 3338–3342. https://doi.org/10.1210/jcem.85.9.6839 (2000).
Article CAS PubMed Google Scholar
Kraakman, M. J., Murphy, A. J., Jandeleit-Dahm, K. & Kammoun, H. L. Macrophage polarization in obesity and type 2 diabetes: Weighing down our understanding of macrophage function?. Front. Immunol. 5, 470. https://doi.org/10.3389/fimmu.2014.00470 (2014).
Article CAS PubMed PubMed Central Google Scholar
Di Carlo, S. E. & Peduto, L. The perivascular origin of pathological fibroblasts. J. Clin. Investig. 128, 54–63. https://doi.org/10.1172/jci93558 (2018).
Article PubMed PubMed Central Google Scholar
Lane, S. W., Williams, D. A. & Watt, F. M. Modulating the stem cell niche for tissue regeneration. Nat. Biotechnol. 32, 795–803. https://doi.org/10.1038/nbt.2978 (2014).
Article CAS PubMed PubMed Central Google Scholar
Lee, H., Lee, I. S. & Choue, R. Obesity, inflammation and diet. Pediatr. Gastroenterol. Hepatol. Nutr. 16, 143–152. https://doi.org/10.5223/pghn.2013.16.3.143 (2013).
Article PubMed PubMed Central Google Scholar
Mathew, S. A., Chandravanshi, B. & Bhonde, R. Hypoxia primed placental mesenchymal stem cells for wound healing. Life Sci. 182, 85–92. https://doi.org/10.1016/j.lfs.2017.06.016 (2017).
Article CAS PubMed Google Scholar
Mathew, S. A. & Bhonde, R. R. Omega-3 polyunsaturated fatty acids promote angiogenesis in placenta derived mesenchymal stromal cells. Pharmacol. Res. 132, 90–98. https://doi.org/10.1016/j.phrs.2018.04.002 (2018).
Article CAS PubMed Google Scholar
Li, M. et al. In vivo human adipose-derived mesenchymal stem cell tracking after intra-articular delivery in a rat osteoarthritis model. Stem Cell Res.Ther 7, 160. https://doi.org/10.1186/s13287-016-0420-2 (2016).
Article CAS PubMed PubMed Central Google Scholar
Roman, E. A. et al. Central leptin action improves skeletal muscle AKT, AMPK, and PGC1 alpha activation by hypothalamic PI3K-dependent mechanism. Mol. Cell. Endocrinol. 314, 62–69. https://doi.org/10.1016/j.mce.2009.08.007 (2010).
Article CAS PubMed Google Scholar
Wong, N. et al. Deficiency in interferon-gamma results in reduced body weight and better glucose tolerance in mice. Endocrinology 152, 3690–3699. https://doi.org/10.1210/en.2011-0288 (2011).
Article CAS PubMed Google Scholar
Lecube, A., Hernández, C., Genescà, J. & Simó, R. Proinflammatory cytokines, insulin resistance, and insulin secretion in chronic hepatitis C patients: A case-control study. Diabetes Care 29, 1096–1101. https://doi.org/10.2337/diacare.2951096 (2006).
Article CAS PubMed Google Scholar
Zheng, C. et al. CD11b regulates obesity-induced insulin resistance via limiting alternative activation and proliferation of adipose tissue macrophages. Proc. Natl. Acad. Sci. USA. 112, E7239-7248. https://doi.org/10.1073/pnas.1500396113 (2015).
Article CAS PubMed PubMed Central Google Scholar
Mungamuri, S. K. et al. USP7 Enforces heterochromatinization of p53 target promoters by protecting SUV39H1 from MDM2-mediated degradation. Cell Rep. 14, 2528–2537. https://doi.org/10.1016/j.celrep.2016.02.049 (2016).
Article CAS PubMed PubMed Central Google Scholar
TeSlaa, T. & Teitell, M. A. Techniques to monitor glycolysis. Methods Enzymol. 542, 91–114. https://doi.org/10.1016/b978-0-12-416618-9.00005-4 (2014).
Article CAS PubMed PubMed Central Google Scholar
Jiang, H. et al. A UPLC-MS/MS application for comparisons of the hepatotoxicity of raw and processed Xanthii Fructus by energy metabolites. RSC Adv. 9, 2756–2762. https://doi.org/10.1039/C8RA08272C (2019).
Article ADS CAS PubMed PubMed Central Google Scholar
Wang, X. L. et al. Free fatty acids inhibit insulin signaling-stimulated endothelial nitric oxide synthase activation through upregulating PTEN or inhibiting Akt kinase. Diabetes 55, 2301–2310. https://doi.org/10.2337/db05-1574 (2006).
Article CAS PubMed Google Scholar
Mungamuri, S. K., Wang, S., Manfredi, J. J., Gu, W. & Aaronson, S. A. Ash2L enables P53-dependent apoptosis by favoring stable transcription pre-initiation complex formation on its pro-apoptotic target promoters. Oncogene 34, 2461–2470. https://doi.org/10.1038/onc.2014.198 (2015).
Article CAS PubMed Google Scholar

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Acknowledgements

The authors acknowledge Dr. R. Hemalatha, Director, ICMR-NIN, for providing the necessary funding and infrastructure to conduct the present study. We also acknowledge the support extended by the ICMR-NIN Animal Facility for conducting the animal experiments. KN received a Senior Research Fellowship (5/3/8/31/ITR-F/2018-ITR) from ICMR. The present research is supported by ICMR-NIN intramural funding (Code: 15-BS03) to Dr. VV, which is greatly acknowledged.

Funding

The present research was carried out by ICMR-NIN intramural funding (Code: 15-BS03, 18-BS10) to Dr. VV, which is greatly acknowledged. KN received Senior Research Fellowship (5/3/8/31/ITR-F/2018-ITR) from ICMR for the present study.

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Bhonde R.
Present address: Dr. D. Y. Patil Vidyapeeth, Pune, 411018, India

Authors and Affiliations

Division of Cell and Molecular Biology, ICMR-National Institute of Nutrition, Jamai-Osmania P.O., Tarnaka, Hyderabad, 500007, India
Nagasuryaprasad Kotikalapudi, Samuel Joshua Pragasam Sampath & Vijayalakshmi Venkatesan
Division of Food Safety, ICMR-National Institute of Nutrition, Jamai-Osmania P.O., Tarnaka, Hyderabad, 500007, India
Sinha Sukesh Narayan & Sathish Kumar Mungamuri
Department of Regenerative Medicine, Manipal Institute of Regenerative Medicine, GKVK Post, Bellary Road, Allalasandra, Yelahanka, Bangalore, 560065, India
Bhonde R.
Division of Animal Facility, ICMR-National Institute of Nutrition, Jamai-Osmania P.O., Tarnaka, Hyderabad, 500007, India
Harishankar Nemani

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Nagasuryaprasad Kotikalapudi
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Samuel Joshua Pragasam Sampath
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Sinha Sukesh Narayan
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Bhonde R.
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Harishankar Nemani
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Sathish Kumar Mungamuri
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Vijayalakshmi Venkatesan
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Contributions

K.N. carried out the majority of experiments, characterized, and injected P-MSCs, including animal maintenance. S.S.J.P. prepared, characterized, and injected P-MSCs into rats. S.N.S. performed metabolite analysis using LC–MS/MS. R.R.B involved in human placenta collection, human ethical approval as well as isolation of P-MSCs. N.H. was involved in vivo imaging. S.K.M. contributed to designing some experiments, configuration of figures, and preparation of the manuscript. V.V. coordinated the overall study, including the project design and manuscript preparation.

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Correspondence to Vijayalakshmi Venkatesan.

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The original online version of this Article was revised: The original version of this Article contained an error in the spelling of the author Bhonde R which was incorrectly given as Bhonde Ramesh R.

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Kotikalapudi, N., Sampath, S.J.P., Sukesh Narayan, S. et al. The promise(s) of mesenchymal stem cell therapy in averting preclinical diabetes: lessons from in vivo and in vitro model systems. Sci Rep 11, 16983 (2021). https://doi.org/10.1038/s41598-021-96121-0

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Received: 14 January 2021
Accepted: 04 August 2021
Published: 20 August 2021
DOI: https://doi.org/10.1038/s41598-021-96121-0

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Abstract

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The therapeutic effects of adipose-derived mesenchymal stem cells on obesity and its associated diseases in diet-induced obese mice

Human adipose tissue mesenchymal stem cells as a novel treatment modality for correcting obesity induced metabolic dysregulation

Adipokines at the crossroads of obesity and mesenchymal stem cell therapy

Introduction

Results

In vitro characterization of P-MSCs

P-MSCs home to the visceral region in WNIN/GR-Ob (Ob-T2D) rats

P-MSCs treatment clears peripheral blood glucose and restores insulin utilization in WNIN/GR-Ob (Ob-T2D) rats

P-MSCs treatment restores the cytokine expression of the WNIN/GR-Ob (Ob-T2D) rats

P-MSCs treatment reduces the macrophage infiltration into adipose tissues of the WNIN/GR-Ob (Ob-T2D) rats

P-MSCs treatment restores glucose homeostasis in the adipose tissues of WNIN/GR-Ob (Ob-T2D) rats

P-MSCs treatment upregulates the PI3K-Akt signaling in adipose tissues and restores the Glut4 expression in the WNIN/GR-Ob (Ob-T2D) rats

P-MSCs enhance the glucose uptake by the adipocytes under the obesogenic milieu—an in vitro approach

P-MSCs induce Glut4 surface translocation in adipocytes under obesogenic conditions in a PI3K-Akt-dependent mechanism

Discussion

Materials and methods

Isolation, expansion, and characterization of human P-MSCs

Animal model and study design

P-MSCs tracking in vivo

Glucose and insulin tolerance test (GTT/ITT)

Enzyme-linked immunosorbent assay

Measurement of serum and tissue cytokines (Dot Blot)

Measurement of serum and tissue cytokine levels

CD11b study by flow cytometer

Real-time quantitative PCR (cytokines markers)

Glucose transport assay

Glycolysis enzyme activity assays

Metabolomic analysis by LC–MS

Cell line and growth conditions

Glucose transport assay

Immunofluorescence

Western blotting analysis (insulin signaling pathway)

Statistical analysis

Ethics approval

Change history

28 September 2021

References

Acknowledgements

Funding

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Authors and Affiliations

Contributions

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Supplementary Information

Supplementary Information.

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Placental mesenchymal stem cells restore glucose and energy homeostasis in obesogenic adipocytes

Human placental mesenchymal stromal cell therapy restores the cytokine efflux and insulin signaling in the skeletal muscle of obesity-induced type 2 diabetes rat model

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