Therapeutic effects of mesenchymal stem cell-derived microvesicles on pulmonary arterial hypertension in rats

Abstract

Aim:

Microvesicles (MVs) are nanoscale membrane fragments released from virtually all cell types upon activation or apoptosis, and may contribute to the beneficial effects of stem cell therapy. In this study, we investigated the therapeutic effects of mesenchymal stem cell (MSC) derived MVs (MSC-MVs) on pulmonary artery hypertension (PAH) in rats.

Methods:

MSC-MVs were isolated from rat bone marrow MSCs that were cultured in a serum-free conditioned medium. Transmission electron microscopy (TEM), flow cytometry and nanoparticle tracking analysis (NTA) were used to characterize the MVs. Adult SD rats were injected with monocrotaline (50 mg/kg, sc) to induce PAH. Three weeks later, the rats were intravenously injected with MSCs, MSC-MVs or saline for 2 weeks. At the end of treatments, the hemodynamic parameters and pathological right ventricular and pulmonary arterial remodeling were analyzed in each group.

Results:

The MSC-MVs showed general morphologic characteristics of MVs and expressed annexin V and CD29 markers under TEM, and their size ranged from 40 to 300 nm. Intravenous injection of MSC-MVs or MSCs significantly ameliorated the mean pulmonary artery pressure (mPAP) and mean right ventricle pressure (mRVP) in PAH rats. Furthermore, intravenous injection of MSC-MVs or MSCs significantly decreased the right ventricle (RV) hypertrophy and pulmonary arteriole area index (AI) and thickness index (TI) in PAH rats.

Conclusion:

Intravenous injection of MSC-MVs or MSCs produces similar beneficial effects for treating PAH, and our results provide a basis for cell-free approach in stem cell therapy.

Introduction

Pulmonary artery hypertension (PAH) is a progressive chronic disease with a high mortality rate. PAH is characterized by increased pulmonary arterial pressure, which results in the right ventricle (RV) hypertrophy and ultimately RV failure1. Current treatments for PAH include endothelin receptor blockers, prostanoids and calcium channel blockers2. Recently, cell-based therapy has emerged as a promising approach for PAH. Intravenous injection of bone marrow-derived progenitors3 or mesenchymal stem cells (MSCs)4 has been shown to inhibit arteriole thickening and to improve the RV function in a rat PAH model. In addition, intratracheal application of MSCs has been shown to restore the pulmonary response to acetylcholine and decrease pulmonary arterial pressure, with no detectable immunolabeled MSCs in the walls of pulmonary vessels5. This study provides good evidence supporting the paracrine effect of stem cell-based therapy. However, the detailed mechanism needs in-depth exploration.

Microvesicles (MVs) are nanoscale membrane fragments that can be released from virtually all cell types upon activation or apoptosis. MVs carry cargo, including specific proteins, mRNAs and microRNAs of their parent cells, and participate in cell-to-cell communication6. The therapeutic effects of MVs have been actively investigated in animal models of various diseases. For example, MSC-MV transplantation could protect kidneys from ischemia/reperfusion-induced injury and chronic renal damage by stimulating proliferation and inhibiting the apoptosis of tubular epithelial cells7,8,9. Intravenous administration of MSC-MVs has been shown to improve neurogenesis and angiogenesis in an ischemic stroke model10. We found that endothelial progenitor cell-MVs could protect endothelial cells against hypoxia-induced injury in in vitro culture systems11. Furthermore, a recent study indicated that MSC-MVs acquire the function of MSCs and can inhibit vascular remodeling and hypoxic pulmonary hypertension in a hypoxia-induced pulmonary hypertension mouse model12, indicating a novel application for stem cell-based therapy.

In this study, we aimed to investigate the therapeutic effects of MSC-MVs for treating PAH in a monocrotaline (MCT)-induced PAH rat model.

Materials and methods

Animals and study design

Sprague Dawley (SD) rats (2–8 weeks old) were purchased from the Animal Experimental Center of Guangdong Province (Guangzhou, China) and housed in the animal care facility at the Affiliated Hospital of Guangdong Medical College. All rats were kept under standard temperature, humidity, and time light conditions and fed standard chow and water ad libitum. All experimental protocols were approved by the Institutional Animal Care and Use Committee of the Affiliated Hospital of Guangdong Medical College.

Monocrotaline (MCT) was diluted in saline before injection as previously described13. On d 1, SD rats (6–8 weeks old) received a single subcutaneous injection of MCT (50 mg/kg body weight) to induce PAH (n=21), or saline alone to serve as a control group (n=7). After 3 weeks, the rats injected with MCT were randomly assigned to 3 groups (n=7/group): vehicle (saline), MSC (treated with 1×106 cells/100 μL saline, once), and MSC-MV (treated with 30 μg/100 μL saline, once/2 d for 2 weeks). At the end of the experiment, the hemodynamic parameters and pathological right ventricular (RV) and pulmonary arterial remodeling were analyzed in each group.

Isolation, culture, and characterization of MSCs

MSCs were isolated from the bone marrow of rats as we previously described7. Briefly, after the rat was sacrificed, the femurs and tibias were removed and cleaned. Cells were collected and dispensed in a 15-mL centrifuge tube, centrifuged at 200×g for 6 min, and resuspended with MSC culture medium, which was composed of α-minimal essential medium (α-MEM, Gibco, NY, USA) supplemented with 10% FBS and 1% antibiotic-antimycotic solution. Cells were plated in a culture dish and cultured in a humidified 5% CO2/95% air incubator.

Flow cytometry analysis was performed to identify cultured cells7. In brief, cells were detached using trypsin-EDTA, centrifuged and incubated with PE-conjugated antibodies in a final volume of 100 mL for 30 min at 4 °C in the dark. Antibodies (PE-conjugated anti-CD29, PE-conjugated anti-CD45, PE-conjugated anti-CD31, and PE-conjugated mouse IgG1 isotype controls) were purchased from BD Biosciences (San Jose, CA, USA). The concentrations of antibodies were applied according to the manufacturer's instructions. Labeled cells were washed and analyzed using flow cytometric analysis (Coulter Epics XL_MCL flow cytometer; Beckman Coulter). A total of at least 10 000 events were collected and analyzed.

The multipotent differentiation ability of cultured cells was evaluated as previously reported4. For adipogenic differentiation, 5×103 cells/well were seeded in a 12-well culture plate and cultured with adipogenic differentiation medium, which was composed of DMEM (Gibco, NY, USA) supplemented with 10% FBS, 10 μg/mL insulin (Sigma, MO, USA), 1 μmol/L dexamethasone (Sigma, MO, USA), 200 μmol/L indomethacin (Sigma, MO, USA), 0.5 mmol/L IBMX (Sigma, MO, USA) and 1% antibiotic-antimycotic solution (Gibco, NY, USA) for 3 weeks. The medium was changed every 3–4 d. Lipid accumulation was assessed by oil red O staining of the cultures (15 mg of oil red O/mL of 60% isopropanol). For osteogenic differentiation, 5×103 cells/well were seeded in a 12-well culture plate and cultured with osteogenic differentiation medium, DMEM supplemented with 10 mmol/L β-glycerophosphate, 50 μg/mL ascorbic acid, and 100 nmol/L dexamethasone (all were purchased from Sigma) for 3 weeks. The medium was changed every 3–4 d. Calcium deposits were visualized by staining with 2% alizarine red S in 0.5% NH4OH (pH=5.5). All experiments were conducted in triplicate.

Collection and characterization of MSC-MVs

MSC-MVs were obtained from MSC conditioned culture medium according to a previously described protocol with slight modifications7. Briefly, MSCs were cultured in serum-free α-MEM for 24 h. Then, the cell culture medium was collected, centrifuged at 2000×g for 20 min to remove cells and debris. The supernatants were ultracentrifuged at 100 000×g for 1 h to pellet the MVs. The protein concentration of the MV preparations was quantified by the Bradford method (Bio-Rad, Hercules, USA).

MSC-MVs were characterized using flow cytometry, transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA). For flow cytometry analysis, MSC-MVs were resuspended and incubated for 30 min at 4 °C in the dark with PE-conjugated CD29 and FITC-conjugated annexin V. An isotype-matched (IgG) nonspecific antibody served as a negative control. All antibodies were purchased from BD Biosciences (San Jose, CA, USA). After incubation, labeled cells were washed with PBS three times and resuspended with 70 μL of PBS for flow cytometric analysis (Coulter Epics XL_MCL flow cytometer; Beckman Coulter). For TEM analysis, MVs were resuspended in PBS and loaded onto mesh nickel Formvar carbon coated grids (Electron Microscopy Science, Hatfield, PA, USA). Excess fluid was removed with filter paper, and the samples were stained with 1% uranyl acetate for 30 s and then washed, dried and stained with 2% lead citrate for another 30 s. The grids were examined under a transmission electron microscope. All experiments were conducted in triplicate.

The size of the collected MSC-MVs was analyzed using a NanoSight NS300 with a 405-nm laser (NanoSight Ltd, Amesbury, UK) according to the previously described method14. Briefly, approximately 0.3 mL of MSC-MVs resuspended in PBS were loaded into the chamber of an NS300 unit. A 405-nm laser beam was used to highlight the particles, which act as point scatters. Three 60-second videos were taken. A minimum of 200 completed particle tracks in each video was analyzed by NTA2.3 software. The velocity of particle movement was used to calculate particle size using the two dimensional Stokes-Einstein equation.

Tail vein injection of MSC-MVs and MSCs

After 3 weeks of MCT injection, rats received MSC or MSC-MV administration via the tail vein as we previously described15. Briefly, MSCs (1×106/100 μL) were slowly injected via the tail vein once4. MSC-MVs (30 μg/100 μL) were injected on alternate days for 2 weeks according to a previous report7. In the control and vehicle groups, rats received 100 μL of saline via tail vein injection.

Measurement of pulmonary hemodynamics

Pulmonary hemodynamics were measured as previous described16. Briefly, 2 weeks after MCT administration, the experimental rats were anesthetized. Then, a polyethylene catheter filled with 2% sodium heparin was inserted into the RV through the jugular vein and the carotid artery for hemodynamic measurements. The RV systolic pressure and systemic blood pressure were measured by a pressure-conductance catheter (model FT212, SciSense, Canada) coupled with a polygraph system (Medlab, Nanjing, China).

Assessment of right heart hypertrophy

After systemic arterial and RV pressures had been recorded, the rats were euthanized, and the lungs and hearts were isolated. The RV, left ventricle (LV) and ventricular septum (VS) were collected, dried with filter paper and weighed. RV hypertrophy was expressed as RV/(LV+VS).

Evaluation of pulmonary arteriole remodeling

After aortic perfusion with 4% PFA, the lungs were excised and fixed in 4% PFA overnight at 4 °C followed by paraffin embedding. Then, lung sections (4 μm) were prepared and stained with hematoxylin and eosin (H&E). Sections were examined under a light microscope (Olympus, Japan). The pulmonary arteriole wall thickness index (TI) and area index (AI) were calculated by the following formulas: TI=(external diameter-internal diameter)/external diameter×100% and AI=(cross section area-lumen area)/cross section area×100%. The mean TI and AI were calculated from 5 random cross sections of each pulmonary arteriole.

Statistical analysis

Data were expressed as the mean±SEM. Comparisons of two groups were performed by Student's t-test. Multiple comparisons were performed by one- or two-way ANOVA. SPSS software version 17.0 was used. For all tests, P<0.05 was considered to be statistically significant.

Results

MSCs were positive for specific stromal cell markers and could be differentiated into adipocytes and osteocytes

The cultured cells displayed a fibroblast-like morphology (Figure 1A). As determined by flow cytometric analysis, cultured cells positively expressed the stromal stem cell marker CD29 (Figure 1B) and negatively stained with hematopoietic lineage markers CD31 and CD45 (Figure 1C and 1D). The differentiation capacity of MSCs was revealed by the successful differentiation of MSCs into osteocytes, with calcium deposition within the cells (Figure 1E), and adipocytes, confirmed by the accumulation of lipid droplets in the vacuoles (Figure 1F).

Figure 1
figure1

MSC culture and characterization. (A) A representative plot shows the fibroblast-like morphology of cultured MSCs. (B–D) Representative flow cytometry plots show the expression of CD29, but not CD31 and CD45, in cultured MSCs. Left curves, isotype control; Right curves, antibodies. (E) Osteogenic differentiation capacity of MSCs confirmed by alizarin red S staining. (F) Adipogenic differentiation capacity of MSCs determined using oil red O staining. Magnification in A, E, and F: ×10.

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Characterization of MSC-MVs

MSC-MVs were generated from MSCs exposed to serum-free medium as described in the Materials and methods. The flow cytometry results revealed that the majority of MSC-MVs had externalized phosphatidylserine, which was detected by annexin V staining, and expressed the MSC specific marker CD29 (Figure 2B). In addition, MSC-MVs displayed a spherical shape under TEM, as indicated by arrows (Figure 2C). Figure 2D showed that the size of MSC-MVs mainly (>95%) ranged from 40 to 300 nm with a peak size of approximately 134 nm, as analyzed by NTA. These data confirm the proper isolation of MSC-MVs in our study.

Figure 2
figure2

MSC-MVs characterized by flow cytometry, transmission electron microscopy and NTA. (A) Isotype controls for MSC-MVs. (B) Annexin V and MSC-specific marker CD29 on MSC-MVs. (C) MSC-MVs viewed under transmission electron microscope. Arrows indicate MSC-MVs. Scale bar: 0.2 μm. (D) Representative graph shows the size distribution of MSC-MVs as determined by NTA.

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MSC-MVs and MSCs significantly attenuated mPAP and mRVP in PAH rats

At week 5 after MCT injection, pulmonary hemodynamics were measured in all rats. Representative pressure curves of mPAP and mRVP are shown in Figure 3A1-3A4. The PAH model was produced successfully as revealed by a higher mPAP in the vehicle group than in the control group (P<0.01; n=7/group). Also, mPAP was attenuated in the MSC-MV and MSC groups compared to the vehicle group but was higher than that in the control group (P<0.01; n=7/group) (Figure 3B). There was no difference in mPAP between the MSC and MSC-MV groups (P>0.05; n=7/group). Similarly, mRVP was lower in the MSC-MV and MSC groups than that in the vehicle group but was higher than that in the control group (P<0.01; n=7/group). Also, there was no significant difference in these variables between the MSC and MSC-MV groups (P>0.05; n=7/group).

Figure 3
figure3

MSC-MVs and MSCs alleviate mPAP and mRVP in PAH rats. (A1–A4) Representative traces show the mPAP and mRVP in control, vehicle, MSC, and MSC-MV groups. (B and C) Summarized data of mPAP and mRVP in different groups. Data are expressed as the mean±SEM. n=7/group. cP<0.01 vs control. fP<0.01 vs vehicle. mPAP, mean pulmonary artery pressure; mRVP, mean right ventricle pressure; RV, right ventricle; PAH, pulmonary artery hypertension.

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MSC-MV treatment significantly decreased RV hypertrophy in PAH rats

RV hypertrophy was quantified by the weight ratio of RV/(LV+VS). The weight ratio of RV/(LV+VS) in the MSC-MV group was significantly lower than that in the vehicle group but was higher than that in the control group (P<0.01; n=7/group) (Figure 4A). In the MSC group, the average ratio of RV/(LV+VS) was not different from that in MSC-MV group (P>0.05; n=7/group).

Figure 4
figure4

MSC-MVs and MSCs alleviate RV hypertrophy and pulmonary artery remodeling in PAH rats. (A) Weight ratio of RV to left ventricle (LV)+ventricle septum (VS) in control, vehicle, MSC, and MSC-MV groups. (B) Representative images of the pulmonary arteriole in different groups. Scale bar: 50 μm. (C and D) Summarized data of the pulmonary arteriole TI and AI in different groups. Data are expressed as the mean±SEM. n=7/group. cP<0.01 vs control; fP<0.01 vs vehicle. PAH, pulmonary artery hypertension; TI, thickness index; AI, area index.

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MSC-MV administration reduced pulmonary arteriole remodeling

H&E staining demonstrated the wall thickening and luminal stenosis in the four different groups (Figure 4B). The pulmonary arteriole thickness index (TI) and area index (AI) were significantly decreased in the MSC-MV and MSC groups compared to those in the vehicle group and were higher than those in the control group (P<0.01; n= 7/group; Figure 4C and 4D). Again, there were no significant differences in these variables between the MSC and MSC-MV groups (P>0.05; n=7/group).

Discussion

The major finding in this study is that the intravenous injection of MSC-MVs or MSCs could similarly decrease pulmonary pressure and RV pressure and reduce RV hypertrophy and pulmonary arteriole remodeling during the development of PAH in rats.

PAH is a life-threatening disease resulting from a variety of heart and lung diseases. The main pathological changes in PAH include persistent pulmonary artery hypertension, pulmonary vascular intima thickening, severe hypoxia, and eventually right heart remodeling and failure17. Clinically, PAH is refractory to most conventional pharmacological therapies. Stem cell transplantation therapy has been shown to improve the vascular endothelial function of the pulmonary arteries3,13,18, and their therapeutic potential for PAH has been recognized in several studies4,5,19,20. Bone marrow-derived MSCs could improve RV function and decrease pulmonary arteriolar wall thickness and area in MCT-induced PAH rats4. Two other groups have shown that the intratracheal administration of MSCs could attenuate pulmonary artery hypertension and pulmonary vascular resistance in PAH mice5,21. In the early stage (1 week after MCT administration) of PAH development, MSC treatment has been demonstrated to attenuate PAP and pulmonary remodeling, which are accompanied by the inhibition of the transforming growth factor β (TGFβ)/Smad2 signaling pathway21. In addition, because transplanted MSCs were found in the lung parenchyma instead of the walls of pulmonary vessels, the paracrine effects of MSCs should be responsible for the role of MSCs in pulmonary remodeling. Indeed, the paracrine mechanism has been proposed to be one of the underlying mechanisms that contributes to the therapeutic effect of transplanted stem cells7,8,22.

MVs are small heterogeneous extracellular vesicles that have been isolated from diverse cell types, including platelets, dendritic cells, endothelial cells, and MSCs. The proteins and genetic materials (mRNAs and microRNAs) carried by MVs could be transferred to target neighboring and distant cells. Accumulating evidence has indicated that MVs could modulate various processes, such as vascular function, angiogenesis, cell proliferation, inflammation, and coagulation10,23,24. Cord blood-derived MSC-MVs may promote angiogenesis in vitro and in vivo25. A recent study showed that the administration of MSC-exosomes can promote functional recovery and neurovascular plasticity in a stroke model10. Later on, this group reported that the protective mechanism of MSC-exosomes is through transferring microRNA-133b to astrocytes and neurons26. Additionally, MSC-MVs have been shown to protect kidneys against injury via stimulating proliferation and decreasing the apoptosis of tubular epithelial cells7,8,9.

In the present study, the isolated MSC-MVs positively stained with annexin V and the MSC specific marker CD29 and displayed MV general spherical characteristics under TEM. According to the latest report from the International Society for Extracellular Vesicles (ISEV), MVs and exosomes are two major types of extracellular vesicles that can be differentiated by their size and content27. Exosomes are defined as extracellular vesicles ranging from 40 to 100 nm in size, and MVs are those with a larger size (100–1000 nm)28. However, Taylor's group found that 100–180-nm vesicles exhibit CD63, a typical marker of exosomes, as determined by NTA29 . In Lee's study, the “exosomes” were isolated through low-speed centrifugations followed by filtering the culture medium through a 0.2-μm filter and then pelleting by ultracentrifugation12. In our study, we isolated the vesicles by the same procedures, except for filtration through a filter. The NTA results showed that the size of these MSC-MVs mainly (>95%) ranged from 40 to 300 nm. To investigate the possible effects of MSC-MVs on treating PAH, we systemically administered MSC-MVs to an MCT-induced PAH rat model. Our data revealed that MSC-MV treatment attenuated mPAP and mRVP in PAH rats compared to the vehicle group, with similar effects on the MSC treatment group. We also observed that MSC-MV treatment reduced RV hypertrophy. Furthermore, pulmonary arteriole wall thickness and area were decreased, as revealed by H&E staining of the lung tissue in the MSC-MV group. These data are in agreement with a previous study showing that the intravenous injection of MSCs can improve RV function in MCT-induced PAH mice4 and are also supported by Lee's findings in a hypoxia-induced PAH mouse model12.

MicroRNAs are small endogenous non-coding RNAs that regulate a wide range of biological processes, including cell apoptosis, differentiation, and cell proliferation. Extracellular vesicles are the main vehicles for circulating microRNAs and have been considered to be a novel mechanism of cell-to-cell communication30. Recent studies have shown that microRNAs carried by exosomes play a critical role in treating stroke26 and hypoxia-induced PAH12 via regulating the gene expression of recipient cells. Based on these observations, we speculate that MSC-MV-carried microRNAs could contribute to the protective effect of MSC-MVs in our study. Although the precise mechanism of MSC-MV-mediated effects needs further investigation, our work provides an explanation for the observed effects of MSCs. Of note, there could be several benefits of using MVs versus cells. First, MVs should easily pass through the capillary network because they are nanoscale vesicles. Second, the potential risk of cell transplantation could be avoided.

In conclusion, our data demonstrate that MSC-MV treatment could attenuate mPAP and mRVP, and reduce RV hypertrophy and pulmonary remodeling in a MCT-induced PAH rat model. These data suggest that MSC-MVs could serve as a novel cell-free therapeutic source for treating PAH.

Author contribution

Jian-ying CHEN and Yan-fang CHEN designed the study; Ran AN, Zhen-jun LIU, Jing-hu LIU, Mian-ming HONG, and Meng-yuan XIAO conducted the experiment; Jian-ying CHEN, Ran AN, Jin-ju WANG, and Shu-zhen CHEN analyzed the data; and Jian-ying CHEN, Jin-ju WANG, Shu-zhen CHEN, and Yan-fang CHEN wrote the paper.

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Acknowledgements

This work was supported by the National Heart, Lung, and Blood Institute (HL-098637 to Yan-fang CHEN), National Natural Science Foundation of China (81370242 and 81270195), Guangdong Natural Science Foundation (S2013010015005), Science and Technology Planning Project of Guangdong Province (2012B031800224 and 2011B031800249), and Science and Technology Innovation Fund of Guangdong Medical College (STIF201128).

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Chen, Jy., An, R., Liu, Zj. et al. Therapeutic effects of mesenchymal stem cell-derived microvesicles on pulmonary arterial hypertension in rats. Acta Pharmacol Sin 35, 1121–1128 (2014). https://doi.org/10.1038/aps.2014.61

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Keywords

  • stem cell therapy
  • bone marrow mesenchymal stem cell
  • microvesicle
  • pulmonary artery hypertension
  • chronic heart disease

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