No current clinical intervention can alter the course of acute spinal cord injury (SCI), or appreciably improve neurological outcome. Mesenchymal stromal cells (MSCs) have been shown to modulate the injury sequelae of SCI largely via paracrine effects, although the mechanisms remain incompletely understood. One potential modality is through secretion of extracellular vesicles (EVs). In this study, we investigate whether systemic administration of EVs isolated from human MSCs (MSCEv) has the potential to be efficacious as an alternative to cell-based therapy for SCI. Additionally, we investigate whether EVs isolated from human MSCs stimulated with pro-inflammatory cytokines have enhanced anti-inflammatory effects when administered after SCI. Immunohistochemistry supported the quantitative analysis, demonstrating a diminished inflammatory response with apparent astrocyte and microglia disorganization in cord tissue up to 10 mm caudal to the injury site. Locomotor recovery scores showed significant improvement among animals treated with MSCEv. Significant increases in mechanical sensitivity threshold were observed in animals treated with EVs from either naïve MSC (MSCEvwt) or stimulated MSC (MSCEv+), with a statistically significant increase in threshold for MSCEv+-treated animals when compared to those that received MSCEvwt. In conclusion, these data show that treatment of acute SCI with extracellular vesicles derived from human MSCs attenuates neuroinflammation and improves functional recovery.
Acute spinal cord injury continues to be a devastating problem worldwide with high morbidity and mortality. Global incidence varied across sixty years from 8 to 246 cases per million each year1,2,3. Incidence in the US is 54 per 1 million annually, averaging approximately 17,500 new cases each year4. The incidence and prevalence of SCI is among the highest in the world, though the proportion of complete transections has been decreasing5. Mortality after hospital admission following acute spinal cord injury ranges from 4.4% to 16.7% globally6. Long term morbidity includes sensory, motor, and autonomic dysfunction.
While there are no effective pharmacological interventions, cell-based therapy has become an appealing alternative. Mesenchymal stromal cells (MSCs) have shown promising wide therapeutic potential in central nervous system trauma, including traumatic brain injury, stroke, and spinal cord injury. The effects of MSCs have been attributed to paracrine support of homeostatic conditions via immunomodulation, angiogenesis and cellular support, leading to recovery of function7,8,9,10,11,12,13,14,15,16,17. In SCI, engraftment of MSCs demonstrated significant therapeutic effects in pre-clinical studies18,19,20,21,22,23,24,25,26,27,28. The communication between stem and injured cells is important for the transmission of trophic signals, however, the details of these processes are not yet understood. One potential mechanism for intercellular exchange is through the secretion of vesicles.
MSCs also have a strong capacity for secretion of extracellular vesicles (EVs) in response to cellular injury29 and EVs isolated from MSCs exhibit stem cell-like regenerative activity30. EVs are small (40 nm-1 μm), heterogeneous particles with a lipid bilayer, containing growth factors, lipids, microRNAs, mRNAs, tRNAs, and proteins31,32,33. Although, their physiologic role is not well elucidated, EVs are suspected to participate in paracrine cellular communication34, provide trophic signals leading to tissue repair29, allow genetic exchange between stem and injured cells35, and attenuate inflammatory responses35. MSC-derived extracellular vesicles (MSCEvwt) can exhibit stem cell-like self-regenerative activity36, but potentially have decreased malignant potential, are less immunogenic, and evade the pulmonary first pass effect relative to MSC37,38.
Recently, we evaluated the immunomodulatory effects of EVs derived from inflammation-stimulated and naïve MSCs (MSCEv+ and MSCEvwt, respectively) using current Good Manufacturing Practice (cGMP)-compliant tangential flow filtration (TFF) system39. Differences in protein composition, cytokine profiles, and RNA content were discovered after detailed characterization of both MSCEvwt and MSCEv+. MSCEv+ attenuated pro-inflammatory cytokine release in vitro compared to MSCEvwt, with different patterns of EV-uptake by activated primary leukocyte subpopulations. Overall, this investigation demonstrated that inflammatory-stimulated MSCs release EVs with enhanced anti-inflammatory properties, partially due to COX2/PGE2 pathway alteration.
In vivo studies have demonstrated potential therapeutic benefits of MSCEv therapy for both acute neurologic injury and neurodegenerative disorders40. Systemic delivery of MSCEvwt in both mouse41 and rat models of traumatic brain injury (TBI)42,43 results in increased angiogenesis, neurogenesis41 and decreased neuroinflammation with concomitant functional recovery42,43. Therefore, we propose that MSCEvwt and MSCEv+ intravenous treatment of spinal cord injured rats will result in significantly improved locomotor recovery, measured by Basso, Beattie, Bresnahan (BBB) Locomotor Rating, and improved mechanical sensitivity measured by the Dixon Up-Down Mechanical Threshold protocol when compared to vehicle-treated controls. We also hypothesize that treatment with MSCEv+ after SCI will result in additionally elevated locomotor and sensory recovery compared to those treated with MSCEvwt. Improvements in functional outcomes in the rat SCI model may be attributed to decreased neuroinflammation and attenuation of secondary injury mechanisms.
Materials and Methods
Isolation and culture of human mesenchymal stromal cells (hMSCs)
hMSCs were isolated from commercially available fresh human bone marrow aspirates of a 34 year old male (AllCells, Alameda, CA) using density centrifugation and plastic adherence as previously described44. An adherent population of MSCs was obtained 3 weeks after the initiation of culture. The cells were screened for typical spindle-like morphology and growth kinetics. The cells were further expanded by plating 106 passage 2 cells at 200 cells/cm2 in 2528 cm² in Nunc™ Cell Factory™ Systems with complete culture medium (CCM) that consisted of α-minimal essential medium (α-MEM; Life Technologies, Grand Island, NY), 17% fetal bovine serum (FBS; Atlanta Biologicals, Norcross, GA), 100 units/ml penicillin (Life Technologies, Carlsbad, CA), 100 μg/ml streptomycin (Life Technologies, Carlsbad, CA), and 2 mM L-glutamine (Life Technologies). At 70% cell confluency, the medium was discarded, the cultures were washed with phosphate-buffered saline (PBS) (Life Technologies, Carlsbad, CA), and the adherent cells harvested with 0.25% trypsin (Life Technologies, Carlsbad, CA) for 5 min at 37 °C and frozen at 106 cells/ml for subsequent experiments as passage 3 cells14. All hMSC used exhibited typical plastic adherence, morphology, and phenotype consistent with the ISCT consensus definition of “MSC” (negative for CD34, CD45, CD19, and HLA-DR, positive for CD44, CD73, and CD90)45,46.
To stimulate the naïve hMSCs, the cells were cultured in the CCM with TNF-α (20 ng/ml) + IFN-γ (20 ng/ml) inflammatory cytokines cocktail overnight. After which, the medium was removed, cells were washed with PBS and fresh serum-free CCM was added. After culturing for another 48 hours, the medium was collected and used for EVs isolation.
Isolation of EVs by sequential filtration
EVs were isolated from both naïve (MSCEvwt) and stimulated MSCs (MSCEv+) as previously described39. We used large format cell culture flasks, and cultured hMSCs (1000 cells/cm2) to ~75% confluency over 5–6 days in 3180 cm2 Corning CellStack Systems (5 layer) to 500 ml serum-free CCM at a time by approximately 18–25 × 106 hMSCs. After 48 hours of culture, the conditioned media was collected and pre-filtered through a 0.2 μm membrane to remove floating cells and cell debris, followed by a volume reduction and buffer exchange using tangential flow filtration (TFF) with a 300 k MW filter cassette (Millipore, Billerica, MA). This allowed large volumes of conditioned media into a concentrated, EV-enriched solution appropriate for use both in vitro and in vivo.
Characterization of EVs
Particle size distribution and quantification by Nanoparticle tracking analysis (NTA)
EVs were characterized for particle size distribution and quantification by Nanoparticle Tracking Analysis (NTA), and expression of surface markers by flow cytometry, as previously described [paper under review]. Samples of extracellular vesicles were quantified via Brownian diffusion size analyses using ZetaView instrumentation (Particle Metrix, Germany). Sample aliquots were diluted 102–106-fold to achieve optimal concentration for analysis; 1.0 mL of diluted sample was used for each analysis. Light scattering of individual particles in solution was digitally recorded, particle trajectory and displacement was automatically analyzed by image analysis tracking software, and the particle-size distribution was determined from the observed Brownian motion of individual particles according to the Stokes-Einstein relationship. MSCEv’s are additionally screened for immunomodulatory activity using a cytokine inhibition assay39 for consistency in potency between preparations and donors, as well as the presentation of typical surface markers by flow cytometry.
Flow cytometry analysis of rat tissue
Microglial isolation and analysis was performed as previously published47. In brief, microglia were isolated by first extracting the spinal cord segments at 14 days post-injury and then mechanical and enzymatic digestion was used to obtain a single-cell suspension using a Neural Cell Dissociation kit (Miltenyi Biotec). We utilized density centrifugation to remove a large amount of myelin, followed by a CD11b/c enrichment using a magnet activated sorting (MACS) kit (Miltenyi Biotec). The resulting myeloid-enriched cells were then stained for CD45CD11, P2Y12, CD32, CD86, CD200R, RT1B, CD163, and a Ghost™ viability dye (TONBO) with the addition of Cyto-Cal™counting beads (Thermo Fisher Scientific). This optimized multicolor immunofluorescence panel (OMIP) was designed to phenotype rat-derived microglia from spinal cord tissue after SCI, and allows for differentiation between macrophages and microglia, as well as phenotypic changes in microglia.
Blood samples were collected and spleens were harvested. Spleens were mechanically dissociated into single cells suspension. Briefly, spleens were placed in C tube (Miltenyi Biotec) and added with 10 ml of PBS. Using Spleen digestion program on the GentleMACS (Miltenyi Biotec), spleens were dissociated for 1 minute, washed twice with PBS and filtered with 70 µm cell strainer. From each sample of blood or spleen 100 µl were added with either lymphoid or myeloid antibody mix. The lymphoid multi-color panel is composed of CD3-FITC (Biolegend cat# 201403), CD25 -PE (Biolegend cat #202105), CD8a–PerCP (Biolegend cat # 201712), CD11b/c-PE Cy7 (BD Biosciences cat # 562222), RT1B-Alexa Fluor 674 (BD Biosciences cat # 562223), CD4-APC Cy7 (Biolegend cat# 201518), CD45RA-V450 (BD Bioscences cat # 561626). The myeloid multi-color panel is composed of His48–FITC (Invitrogen cat# 11057082), CD43-PE (Biolegend cat # 202812), CD8a–PerCP (Biolegend cat # 201712), CD11b/c-PE Cy7 (BD Biosciences cat # 562222), CD161-APC (Biolegend cat# 205606), CD4-APC Cy7 (Biolegend cat# 201518), CD172a-V450 (Biolegend, custom made). Cells were incubated for 20 minutes at room temperature and fixed in TQPrep™ Workstation (Beckman Coulter). Samples were run on Gallios (Beckman Coulter) to collect 10,000 events, and analyzed using Kalusa vr. 1.5a analysis software (Beckman Coulter).
All protocols involving the use of animals were following the National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the University of Texas Health Science Center at Houston Animal Welfare Committee, with is the Institutional Animal Care and Use Committee. Rats were purchased from Envigo (Indianapolis, IN, USA) for use in this study. The animals were housed on a 12 h light/dark cycle with ad libitum access to food and water.
Spinal Cord Contusion and EV treatment
Adult, male Sprague-Dawley rats (Envigo, Harlan, USA) weighing 225–250 g were utilized in this study. Animals were anesthetized with 4% inhaled isoflurane in oxygen and maintained using 1.5 L/min of 2–3% inhaled isoflurane in oxygen throughout the procedure. Animals received a laminectomy at spinal cord thoracic level 10 (T10), and the vertebral column was stabilized at T9 and T11. A moderate contusion injury (150 kdynes of force with 1 s dwell) was delivered to the spinal cord at T10 using the Infinite Horizon Impactor (Precision Systems and Instrumentation, LLC, Fairfax Station, VA), without opening the dura mater48. The overlying muscles were immediately sutured and the skin was closed with stainless steel wound clips. Beginning the day after SCI surgery, each animal’s urinary bladder was manually expressed twice daily until the animal recovered the ability to void its bladder. As a rule, bladder care was ceased when an individual animal exhibited an empty bladder on two consecutive bladder care sessions. To minimize post-surgical pain, animals were treated twice daily for five days post-SCI with buprenorphine (0.02 mg/kg s.q.). To prevent dehydration, animals also received a 3-ml bolus of 0.9% saline s.q. twice daily for the first 72 h after surgery. To prevent infection, animals also received antibiotics (0.01 mg/kg gentamicin i.p.) once daily for 10 days. Animals were housed in groups of two and maintained under normal veterinary care.
Animals were randomly selected to receive either vehicle (phosphate buffered saline solution) or MSCEv injection intravenously via tail vein 3 hrs after sham or spinal cord injury. MSCEvwt and MSCEv+ were injected at a concentration of 1 × 10 9 Ev/ml and a volume of 1 ml.
Longitudinal behavioral was assessed in two cohorts of animals (Sham n = 6, SCI + vehicle n = 6, SCI + MSCEvwt n = 8, SCI + MSCEv+ n = 8). Description of behavioral tasks are described in detail below.
Hind limb Motor Function
Hind limb locomotor function was assessed using the Basso, Beattie and Bresnahan (BBB) open field locomotor scale49. Before SCI surgery, animals were allowed to acclimate to the open field testing environment (a 40′′-diameter plastic wading pool) in groups of four for 10 minutes daily until they ceased to exhibit fear-associated behavior (e.g., crouching, cowering away from the examiner, vocalizing) and displayed signs of comfort (e.g., grooming, accepting treats from the examiner’s hand, exhibiting continuous locomotion and exploration). No further acclimation to the testing environment was performed.
BBB scores were assessed on days 1, 2, 3, 5, 7, 10 and 14 post-injury. Animals were placed into the open field and allowed to freely move about for a period of 4 minutes. Two blinded, independent observers scored each hind limb using a scoring sheet. Hind limb BBB scores were rated using an abbreviated 16-point BBB Open Field Rating Scale, and inter-rater reliability was confirmed. The abbreviated locomotor scoring scale was modified from the 21-point BBB Open Field Rating Scale by Basso, Beattie and Bresnahan49. Due to the brief period of study, the scale was abbreviated to focus on the subtle differences observed in the acute recovery period. In our previous studies of similar length, the observed recovery scores were consistently below 16, making this a reasonable level for abbreviation. In this study, the locomotor scores for both hind paws were averaged to produce one score per test session. Data were analyzed for normality using a Shapiro-Wilk normality test with a confidence interval of 95%. Values were also analyzed for skewness, with the calculated values being between −0.5 and 0.5, the distribution is considered approximately symmetrical. BBB scores were analyzed using a two-way repeated measures ANOVA (factors: experimental groups and time points with repeated measures on the second factor), followed by a Bonferroni post-test.
Mechanical hypersensitivity was defined as a decreased withdrawal threshold when the hind paw was presented with a series of calibrated von Frey monofilaments (Stoelting, Wood Dale, IL), consistent with previous studies50. Animals were habituated to the testing environment for 10 minutes on day 14 post-injury. A series of filaments delivering calibrated amounts of force (2 g to 15 g) were applied using the Dixon “up-down” method, and 50% mechanical withdrawal threshold was determined as previously described50,51. Scores were analyzed using a paired Student’s t test; effectiveness of pairing was determined by calculating the Pearson correlation coefficient (r).
Rats were anesthetized and spinal cord tissue was harvested following perfusion with PBS and 4% PFA 14 days post-injury (Sham n = 2, SCI + vehicle n = 4, SCI + MSCEvwt n = 4, SCI + MSCEv+ n = 4). Coronal sections at 12 µm or sagittal sections at 40 µm were sectioned on a cryostat (Leica CM1860), adhered to glass slides and stained using standard staining protocol. Briefly, the sections were first rinsed with tris buffered saline (TBS) 1X (Thermo Fisher Scientific, PA) three times for 5 minutes each followed by a blocking and permeabilizing step for 1 hour with TBS 1X with 0.3% Triton X-100 and 10% normal goat serum (Jackson Immuno Research, PA) at room temperature. Then they were incubated in primary antibody solution of TBS 1X with 0.025% Triton X-100 and primary antibodies, anti-Iba-1, anti-GFAP, anti-doublecortin or anti-NeuN at 4 °C overnight. Slides were rinsed in TBS 1X three times for 10 minutes each then incubated in secondary antibody solution of TBS 1X with 0.025% Triton X-100 and secondary antibodies at 1:500 for 2 hours at room temperature. The sections were washed thrice with PBST for 10 minutes each after incubation with secondary antibodies. Slides were let dry at room temperature before they were cover-slipped with DAPI Fluoromoun-G (Southern Biotech, Birmingham, AL). Primary antibodies: microglia (Iba-1, 1:500, Wako-chem, Richmond, VA), astrocytes (GFAP, 1:500), regenerating neurons (Doublecortin, 1:300, Temecula, CA), mature neurons (NeuN, 1:500, Millipore Sigma, Billerica, MA). Secondary antibodies: 1:500 Alexa Fluor-488: and 1:500 Alexa Fluor-568:A11011, Invitrogen. Microscopic images were acquired with a Leica DM4000B fluorescence microscope.
Injured subjects were excluded from the study if the actual force of impact to the spinal cord fell outside a range between 150 and 175 Kdynes52. In addition, any injured subjects receiving an impact of force within that range that exhibited a hind limb locomotor score greater than 2 on post-injury day 1 were also excluded49.
All data was analyzed using GraphPad Prism (GraphPad Software, Inc., La Jolla, CA) using an analysis of variance (ANOVA) with Tukey post-hoc analyses for multiple comparisons. Values of p < 0.05 were considered significant. All group data is presented as mean +/− standard error or standard deviation. Sample sizes were determined a priori using G*Power Statistical Power Analyses Software53.
The datasets generated during and/or analyzed during the current study are not publicly available due to inclusion in pending publications but are available from the corresponding author on reasonable request.
MSCEv Attenuate Microglia Activation Pathways
Samples of spinal cord tissue containing the injury epicenter (Fig. 1a) were analyzed by flow cytometry for microglia activation phenotypes. Interestingly, the total number of cells positive for markers associated with pro-inflammatory, M1 microglia (CD32 and CD86) were significantly decreased after treatment with MSCEvwt and MSCEv+ (***p < 0.001, **p < 0.01, respectively) when compared to those that were injured and received vehicle injections (Fig. 1b). Similarly, cells positive for M2 associated markers CD200R, CD163 and RT1B are significantly decreased (**p < 0.01, *p < 0.05, *p < 0.05, respectively) with treatment of either MSCEvwt or MSCEv+ after SCI (Fig. 1b).
Lumbar sections of spinal cord were processed and analyzed. The ratio between the epicenter and the distal lumbar was calculated and was shown to be coherent with the marker expression by showing similar trend of significant reduction following treatment. (Fig. 1c). These results imply that the inflammation caused by the injury is local and that the MSCEv given are able to influence/target the inflammatory site and act locally as well. The expression of M1 associated markers in the CNS, p2y12, is a microglia specific marker. By assuming that microglia are CD11+CD45+ and p2y12+, we were able to extract data and apply this not only to microglia but also to the myeloid cells as the monocytes/macrophages, which we assumed to be CD11+CD45+p2y12−. This analysis revealed that both MSCEV and MSCEV + treatment reduces the expression of RT1B in the monocytes/macrophages (CD11b/c+, CD45+, P2y12−) populations in the spinal cord (Supplemental Figure S1). This data indicates that EVs are effective in reducing neuroinflammation in the injury epicenter as early as 14 days post-injury. SCI + Vehicle, n = 3, SCI + MSCEvwt, n = 3, SCI + MSCEv+, n = 3.
MSCEv treatment following SCI results in improved locomotor recovery
Animals received either sham or T10 contusion SCI and were treated with MSCEv (MSCEvwt and MSCEv+ groups combined) 3hrs after injury. All animals were observed for locomotor recovery using the BBB scale on days 1, 2, 3, 5, 7, 10 and 14 post-injury. SCI + MSCEv animals showed significant improvement in locomotor recovery scores on days 5, 7, and 14 post-injury vs. SCI rats treated with vehicle injections. SCI rats treated with MSCEv scored significantly higher on locomotor recovery assessments compared to untreated animals on post-injury day 5 (***p < 0.001), 7 (**p < 0.01) and 14 (**p < 0.01). (Fig. 2). Sham, n = 6, SCI + Vehicle, n = 6, SCI + MSCEv, n = 16. All data represented are means +/− SD. Data was statistically analyzed using Two-Way ANOVA with Tukey’s multiple comparison test. Raw data is included in Supplemental Table 1.
Mechanical Sensitivity Threshold Improved with MSCEv
In addition to improved locomotor recovery, we observed a significant change in mechanical hypersensitivity after injury. Two weeks after injury we used calibrated von Frey filaments and the Dixon Up-Down scoring method to identify allodynia in hind paws and determine mechanical sensitivity thresholds. SCI animals treated with MSCEv (MSCEvwt or MSCEv+) exhibited significantly higher force threshold (*p < 0.05) than those treated with vehicle when tested with the Dixon Up-Down method for mechanical sensitivity in the hind paws. Sham, n = 6, SCI + Vehicle, n = 6, SCI + MSCEv, n = 16. All data represented are means +/− SD. Data was statistically analyzed using One-Way ANOVA with Sidak’s test for multiple comparisons. (Fig. 3).
Treatment with MSCEv+ from Inflammation-Stimulated MSC Improves Sensory Function
A cohort of SCI animals received injections of extracellular vesicles which were derived from MSC that we stimulated with inflammatory agents. EVs secreted by inflammation-stimulated MSC were then referred to as activated extracellular vesicles (MSCEv+).
Animals treated with MSCEv+ exhibited significantly higher mechanical force threshold (**p < 0.01) than those treated with MSCEvwt when tested with the Dixon Up-Down method for mechanical sensitivity in the hind paws. There was also a significant increase in threshold when treated with MSCEvwt (*p < 0.05), when compared to untreated SCI animals. MSCEv+ displayed an increased therapeutic effect which can be attributed to the enhanced anti-inflammatory properties of MSCEv+ derived from inflammation-stimulated MSCs. Sham + Vehicle, n = 6, SCI + Vehicle, n = 6, SCI + MSCEvwt, n = 8, SCI + MSCEv+, n = 8. Data represent mean values +/− SEM. All data was analyzed for statistical significance using One-Way ANOVA with Sidak’s test for multiple comparisons (Fig. 4).
MSCEv Effects on Immune Response in Blood and Spleen
Using flow cytometry we were able to evaluate lymphoid and myeloid populations in the blood and spleen. The analysis of the myeloid population at 14 days after injury did not show significant changes in the spleen, and seem to be high in all the groups (Fig. 5). However, changes remain visible in the blood; treatment with MSCEv resulted in myeloid cell expansion that persists, while the injured group showed overall reduction in myeloid cells in circulation. Several subpopulations, such as neutrophils, NK cells and granulocyte, were analyzed. Neutrophils (CD43+CD161+) seemed to increase upon injury and remain high after 14 days, in both spleen and blood. Particularly in the blood, treatment with MSCEvwt resulted in elevated levels of Neutrophils as well. NK cells (His48−CD161+) seem to remain at a range of 3–10% in both spleen and blood. Another subpopulation of granulocytes, often refer to as Myeloid-derived suppressor cells (MDSC), which were identified as CD11+CD172+His48+, seemed to expand upon MSCEv treatment in both spleen and blood.
In addition, we evaluated dendritic cells and T cells activation at 14 days. MSCEv groups showed increased levels of dendritic cells (DCs), compared to injured group (Supplemental Figure S2). T cell expansion was not significant between the groups at 14 days. The T cell/DC conjugate is a measurement for activation of the immune system. Indeed, the levels of the conjugates increased following MSCEv treatment, however these results are not significant, but do imply the safety of the treatment. No particular T cell subset expansion was observed. Sham + Vehicle, n = 3, SCI + Vehicle, n = 3, SCI + MSCEvwt, n = 3, SCI + MSCEv+, n = 3.
MSCEv Decreases Reactive Microglia and Astrocytes
In examining representative immunohistochemical images of the epicenter and caudal cord, we noted a relative increase in GFAP signal intensity that directly corresponded with the injury. This increase in GFAP is consistent with the gross anatomical damage associated with spinal cord injury. In reference to coronal sections (Fig. 6), there is a relative loss of structure that is observed in comparing sham images to injured images. Corresponding images from treated animals appear more similar to the sham images. There also appears to be slight, relative variation in Iba-1-labeled structures in injured sections that do not resemble those of sham sections. It is not clear based on limited histology alone if treatment had an effect on these organizational changes, however the differences suspected in astrocyte and microglia may be associated with scar tissue formation. Sham + Vehicle, n = 2, SCI + Vehicle, n = 2, SCI + MSCEvwt, n = 3, SCI + MSCEv+, n = 3. (Fig. 6).
Our data demonstrate that MSCEvwt and MSCEv+ attenuate inflammation and improve functional outcome in a rodent model of SCI. In this study, we utilized a cGMP-compliant system to isolate MSC-derived EVs from normal and inflammatory cytokine-stimulated cultures, which were then delivered intravenously 3 hr after T10 spinal contusion injury. Treatment with MSCEv resulted in an improvement in locomotor recovery, decrease in hyper-sensitivity, and an overall decrease in neuroinflammation. This effect persisted at least 14 d after treatment and is accompanied by differences in the myeloid and lymphoid profile of the blood and spleen. In most circumstances, the MSC-derived EV had no distinguishable differences, with the exception of hypersensitivity, where EV from inflammation-stimulated MSCs were able to significantly improve the treatment effect. Overall, MSCEv were successful in improving outcome after SCI.
Cellular therapies to treat SCI and other CNS injuries have been tested in many experimental animal models and clinical trials, however, the success of these studies is limited. While some studies explore stem-cell based cell and tissue replacement strategies, many studies target therapeutic intervention on secondary injuries in an attempt to limit cell death, spare white matter, and modulate immune responses and neuroinflammation to improve functional recovery. These studies, while promising, often have a number of technical hurdles to overcome and formidable challenges when applied at scale.
Our lab recently developed a multi-parameteric panel to analyze microglia using flow cytometry. This technique can differentiate between macrophages and resident microglia, quantify total cell numbers, as well as phenotypic changes to microglia polarization in rat models of TBI and SCI. Details of this technique can be found in Toledano-Furman et al.47. We observed a number of significant differences in putative pro-and anti-inflammatory populations, although the current understanding of rat CNS immunology has not fully matured. While much work has been devoted to characterizing mouse microglia markers, phenotypic characterization of rat microglia is not yet standardized, resulting in some difficulties in comprehensive data analysis. Our results show a significant decrease in the activation markers, which suggest overall attenuation of the inflammation at the injury site after MSCEvwt or MSCEv+ treatment. This also implies that MSCEv may be capable of preventing a large neuroinflammatory response altogether rather than skewing microglial polarization. Tissue level neuroinflammation has been linked to both locomotor activity and mechanical sensitivity54,55.
Here, we show that animals treated with MSCEv have significantly improved locomotor recovery as early as 5 days post-injury (Fig. 2; *p < 0.001), with increasing significance at days 7, 10, and 14 post-injury when compared to vehicle-treated or MSC-treated SCI animals. In previous studies by our group and others, MSC-treated rats have shown increased threshold to mechanical stimulus and an improvement in locomotor function. In comparing our internal data sets, MSCEv recover locomotor function earlier than those treated with other cellular therapies in parallel studies (data not shown). In addition to locomotor recovery, MSCEv and particularly MSCEv+ were able to decrease mechanical sensitivity 14 d after injury.
In the presence of inflammatory stimuli, immune cells are differentially activated56. Activation causes a number of notable changes in marker expression, as well as proliferation. To better capture the global changes, we quantified cell numbers in addition to profiling marker expression. Evaluating different components of the cellular arm of the immune system revealed overall moderate changes, of which the majority were not significant with limited replicates. At the endpoint of the study, MSCEv treatment resulted in non-significant myeloid cell expansion. Injury resulted in elevated levels of neutrophils in both the spleen and blood. Treatment with MSCEv+, but not MSCEvwt reduced the levels of these cells. Expansion of NK cells and granulocytes was observed in the blood. This granulocytic population was found to have immunosuppressive effects on T cells and macrophages. Saiwai et al.57, demonstrated the function of these myeloid cells in a mouse model of SCI and stated that they significantly contribute to attenuate acute inflammation after SCI.A similar trend was published by Wang et al. in a mouse model of SCI, where 3 days post-injury, blood myeloid cells were increased and maintained high level for at least 28 days post-injury58. Spleen myeloid were also increased on day 3, but rapidly decreased with time. In our study, MSCEv treatment resulted in a reduction in blood myeloid while spleen MDSC increase compared to controls. This result may indicate that MSCEv prevent egress of myeloid cells from the spleen as a method of reducing inflammation. Finally, the different subsets of T cells were evaluated, of which T cytotoxic were significantly increased in the circulation following treatment with MSCEv. The percent of T cell/DC conjugate was increased with treatment, but again, not significantly at that time point. These results were as expected, as systemic treatment with EVs was previously found to result in T cell function modulation59. T regulatory cells increased in the spleen but not in the blood fraction tested. Those results are coherent with previously published work demonstrating elevated levels of T regulatory following MSC exosomes systemic injection60. Overall we concluded that MSCEv treatment modulated the host immune response, at 14 days after injury the cellular components of the immune system support inflammation attenuation and thus tissue regeneration.
Extracellular vesicles (EV) secreted from MSC are of great interest as a new, cell-free therapeutic. To date, there are few studies of MSCEv used to treat CNS trauma, most of which focus upon TBI or stroke using normal or genetically modified MSC. In this study, we investigate whether systemic administration of EVs isolated from MSCs has the potential to be exploited as an alternative to cell-based therapy for SCI. EVs from MSCs were isolated using a current Good Manufacturing Practice (cGMP)-compliant tangential flow filtration system. Isolated EVs were characterized for the expression of surface markers (CD9, CD63, CD81 and CD107a) by flow cytometry and screened for the ability to reduce cytokines and reduce donor-to-donor and batch-to-batch variability. The ZetaView Nanoparticle Tracking Analyzer was used to determine the size distribution and quantitation of the EVs.
MSCEvwt administered 24hrs after TBI in rodent models are reported to significantly improve spatial learning in Morris water maze approximately one month after injury and treatment41,43,61, as well as significantly reduce neurological deficits and foot-fault frequency 2–4 weeks after injury and treatment43. In experimental models of stroke, EVs from MSCs with overexpressed microRNA 133b have improved functional recovery and neuroplasticity compared to rats treated with PBS or control MSCEvwt, possibly due to secondary release of EVs from astrocytes62 downregulating connective tissue growth factor (CTGF)63. In these studies, and in work from other fields, MSCEv have been observed to be capable of replicating some or all of the therapeutic actions attributed to MSC. This includes the capacity to modulate the immune response without acting as a broad immunosuppressant or a traditional anti-inflammatory drug, like methylprednisone. The presence of numerous potential mechanisms of action, even in isolated MSCEv, suggests that it will be difficult to recapitulate their actions through single or combinatorial pharmaceutical treatments.
A single, recent study describes the therapeutic effects of EV from rat MSC on SCI-induced apoptosis, inflammation and angiogenesis. The authors delivered rat MSC-derived EVs systemically 30 minutes after T10 weight-drop contusion and reported a decrease in apoptosis and inflammatory cytokines, improved locomotor recovery, and promoted angiogenesis64. Locomotor recovery in our study supersedes that of BBB scores of SCI + EV animals reported in the literature64, with higher BBB scores at each time point and statistical significance achieved starting 5 days after injury, which is 9 days prior to significance achieved in the Huang et al., study. This difference, while notable, could be explained by either differences in EV potency or differences in experimental methodology. Importantly, our study utilizes cGMP-compatible techniques and reagents to create scalable preparations of human MSC-derived extracellular vesicles in an effort to facilitate and streamline translation to clinical applications.
In this study, we delivered MSCEv 3 hrs post-injury, primarily to translate to real world applications. Specifically, it would be logistically challenging to deliver an experimental therapeutic in less than 3 hrs. This time point has further advantages, as significant BSCB permeability exists between 1hr and 5 days post-injury, with peak permeability at 24hrs post-injury and recovery by 14 days post-injury65. This window allows MSCEv to easily penetrate the BSCB and be present during the initial activation of resident microglia and infiltration of neutrophils66. Inflammatory mediators TNF-α and IL-1β peak within the first 4hrs after SCI in rats67. Rats subjected to SCI have an intraspinal accumulation of circulating monocytes, microglia and lymphocytes peaking at 14 days post-injury. Interestingly, a single treatment of MSCEv at 3 hr was able to significantly affect the immune composition of the blood, spleen, and spinal cord across both myeloid and lymphoid cell populations. It is likely that this effect is due to MSCEv activity during the acute and sub-acute phases of injury, rather than long-term persistence and ongoing activity. While we did not define the persistence and penetration of human MSCEv in this study, other reports indicate that EVs are rapidly removed from circulation with a half-life often measured in minutes68,69.
Broadly, EV efficacy has been attributed to the same mechanisms as MSC, with many reports positing that EVs are more capable of crossing the blood-brain/blood-spinal cord barrier. In a recent paper39, we described how inflammation-stimulated MSC produce extracellular vesicles with increased anti-inflammatory properties in vitro, through the expression of a number of potent immunomodulating cytokines and metabolites, including COX2/PGE2, as well as micro RNA. In another study, we recently demonstrated that MSC decrease neuroinflammation in TBI via the COX2/PGE2 pathway using both a loss-of-function and a gain-of-function assay in vivo 45. The specific mechanism of action MSCEv use to modulate local and systemic inflammation is crucial to optimizing the delivery, dosage, and treatment regimen of MSCEv.
In conclusion, the data generated in this study suggests that MSCEvs are effective in attenuation of neuroinflammation and its effects on functional recovery after SCI in a rodent model. Additionally, treatment with inflammatory cytokine stimulated MSCs resulted in a modified therapeutic profile that demonstrated increased efficacy in some outcome measures.
Furlan, J. C., Sakakibara, B. M., Miller, W. C. & Krassioukov, A. V. Global incidence and prevalence of traumatic spinal cord injury. Can J Neurol Sci 40, 456–464 (2013).
Wyndaele, M. & Wyndaele, J. J. Incidence, prevalence and epidemiology of spinal cord injury: what learns a worldwide literature survey? Spinal Cord 44, 523–529, https://doi.org/10.1038/sj.sc.3101893 (2006).
Lee, B. B., Cripps, R. A., Fitzharris, M. & Wing, P. C. The global map for traumatic spinal cord injury epidemiology: update 2011, global incidence rate. Spinal Cord 52, 110–116, https://doi.org/10.1038/sc.2012.158 (2014).
National Spinal Cord Injury Statistical Center (NSCISC), https://www.nscisc.uab.edu/ (2017).
Devivo, M. J. Epidemiology of traumatic spinal cord injury: trends and future implications. Spinal Cord 50, 365–372, https://doi.org/10.1038/sc.2011.178 (2012).
Sekhon, L. H. & Fehlings, M. G. Epidemiology, demographics, and pathophysiology of acute spinal cord injury. Spine 26, S2–12 (2001).
Boomsma, R. A. & Geenen, D. L. Mesenchymal stem cells secrete multiple cytokines that promote angiogenesis and have contrasting effects on chemotaxis and apoptosis. PLoS One 7, e35685, https://doi.org/10.1371/journal.pone.0035685 (2012).
Nauta, A. J. & Fibbe, W. E. Immunomodulatory properties of mesenchymal stromal cells. Blood 110, 3499–3506, https://doi.org/10.1182/blood-2007-02-069716 (2007).
Uccelli, A., Laroni, A. & Freedman, M. S. Mesenchymal stem cells for the treatment of multiple sclerosis and other neurological diseases. Lancet Neurol 10, 649–656, https://doi.org/10.1016/s1474-4422(11)70121-1 (2011).
Wang, L. T. et al. Human mesenchymal stem cells (MSCs) for treatment towards immune- and inflammation-mediated diseases: review of current clinical trials. J Biomed Sci 23, 76, https://doi.org/10.1186/s12929-016-0289-5 (2016).
Prockop, D. J. & Oh, J. Mesenchymal stem/stromal cells (MSCs): Role as guardians of inflammation. Mol Ther 20, 14–20 (2012).
Wang, Y., Chen, X., Cao, W. & Shi, Y. Plasticity of mesenchymal stem cells in immunomodulation: pathological and therapeutic implications. Nat Immunol 15, 1009–1016 (2014).
Zhang, R. et al. Anti-inflammatory and immunomodulatory mechanisms of mesenchymal stem cell transplantation in experimental traumatic brain injury. J Neuroinflam 10, 106 (2013).
Kota, D. J. et al. Propranolol and Mesenchymal Stromal Cells Combine to Treat Traumatic Brain Injury. Stem Cells Transl Med 5, 33–44, https://doi.org/10.5966/sctm.2015-0065 (2016).
Menge, T. et al. Mesenchymal stem cells regulate blood-brain barrier integrity through TIMP3 release after traumatic brain injury. Sci Transl Med 4, 161ra150 (2012).
Walker, P. A. et al. Bone marrow–derived stromal cell therapy for traumatic brain injury is neuroprotective via stimulation of non-neurologic organ systems. Surgery 152, 790–793 (2012).
Walker, P. et al. Direct intrathecal implantation of mesenchymal stromal cells leads to enhanced neuroprotection via an NFkappaB-mediated increase in interleukin-6 production. Stem Cells Dev 19, 867–876 (2010).
Dasari, V. R., Veeravalli, K. K. & Dinh, D. H. Mesenchymal stem cells in the treatment of spinal cord injuries: A review. World J Stem Cells 6, 120–133, https://doi.org/10.4252/wjsc.v6.i2.120 (2014).
Matyas, J. et al. Effects of Bone-Marrow-Derived MSC Transplantation on Functional Recovery in a Rat Model of Spinal Cord Injury: Comparisons of Transplant Locations and Cell Concentrations. Cell Transplant 26, 1472–1482 (2017).
Oliveri, R., Bello, S. & Biering-Sorenson, F. Mesenchymal stem cells improve locomotor recovery in traumatic spinal cord injury: Systematic review with meta-analyses of rat models. Neurobiology of Disease 62C, 338–353 (2013).
Kim, J., Ha, K., Molon, J. & Kim, Y. Bone marrow-derived mesenchymal stem cell transplantation for chronic spinal cord injury in rats: comparative study between intralesional and intravenous transplantation. Spine 38, E1065–1074 (2013).
Quertainmont, R. et al. Mesenchymal stem cell graft improves recovery after spinal cord injury in adult rats through neurotrophic and pro-angiogenic actions. PLoS One 7, e39500 (2012).
Nakajima, H. et al. Transplantation of mesenchymal stem cells promotes an alternative pathway of macrophage activation and functional recovery after spinal cord injury. J Neurotrauma 29, 1614–1625 (2012).
Novikova, L., Brohlin, M., Kingham, P., Novikov, L. & Wiberg, M. Neuroprotective and growth-promoting effects of bone marrow stromal cells after cerivcal spinal cord injury in adult rats. Cytotherapy 13, 873–887 (2011).
Urdzikova, L. et al. Transplantation of bone marrow stem cells as well as mobilization by granulocyte-colony stimulating factor promotes recovery after spinal cord injury in rats. J Neurotrauma 23, 1379–1391 (2006).
Cizkova, D. et al. Repetitive intrathecal catheter delivery of bone marrow mesenchymal stromal cells improves functional recovery in a rat model of contusive spinal cord injury. J Neurotrauma 28, 1951–1961 (2011).
Ohta, M. et al. Bone marrow stromal cells infused into the cerebrospinal fluid promote functional recovery of the injured rat spinal cord with reduced cavity formation. Exp Neurol 187, 266–278 (2004).
Ritfeld, G. J. et al. Bone marrow stromal cell-mediated tissue sparing enhances functional repair after spinal cord contusion in adult rats. Cell Transplant 21, 1561–1575 (2012).
Baglio, S. R., Pegtel, D. M. & Baldini, N. Mesenchymal stem cell secreted vesicles provide novel opportunities in (stem) cell-free therapy. Front Physiol 3, 359, https://doi.org/10.3389/fphys.2012.00359 (2012).
Bruno, S. & Camussi, G. Role of mesenchymal stem cell-derived microvesicles in tissue repair. Pediatr Nephrol 28, 2249–2254, https://doi.org/10.1007/s00467-013-2413-z (2013).
Vlassov, A. V., Magdaleno, S., Setterquist, R. & Conrad, R. Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochim Biophys Acta 1820, 940–948, https://doi.org/10.1016/j.bbagen.2012.03.017 (2012).
van der Pol, E., Boing, A. N., Harrison, P., Sturk, A. & Nieuwland, R. Classification, functions, and clinical relevance of extracellular vesicles. Pharmacological reviews 64, 676–705, https://doi.org/10.1124/pr.112.005983 (2012).
Lai, R. C. et al. Proteolytic Potential of the MSC Exosome Proteome: Implications for an Exosome-Mediated Delivery of Therapeutic Proteasome. International journal of proteomics 2012, 971907, https://doi.org/10.1155/2012/971907 (2012).
Tetta, C., Ghigo, E., Silengo, L., Deregibus, M. C. & Camussi, G. Extracellular vesicles as an emerging mechanism of cell-to-cell communication. Endocrine 44, 11–19, https://doi.org/10.1007/s12020-012-9839-0 (2013).
Camussi, G., Deregibus, M. C., Bruno, S., Cantaluppi, V. & Biancone, L. Exosomes/microvesicles as a mechanism of cell-to-cell communication. Kidney international 78, 838–848, https://doi.org/10.1038/ki.2010.278 (2010).
Camussi, G., Deregibus, M. C. & Cantaluppi, V. Role of stem-cell-derived microvesicles in the paracrine action of stem cells. Biochemical Society transactions 41, 283–287, https://doi.org/10.1042/bst20120192 (2013).
Koniusz, S. et al. Extracellular Vesicles in Physiology, Pathology, and Therapy of the Immune and Central Nervous System, with Focus on Extracellular Vesicles Derived from Mesenchymal Stem Cells as Therapeutic Tools. Front Cell Neurosci 10, 109, https://doi.org/10.3389/fncel.2016.00109 (2016).
Fischer, U. M. et al. Pulmonary passage is a major obstacle for intravenous stem cell delivery: the pulmonary first-pass effect. Stem cells and development 18, 683–692, https://doi.org/10.1089/scd.2008.0253 (2009).
Harting, M. T. et al. Inflammation-Stimulated Mesenchymal Stromal Cell-Derived Extracellular Vesicles Attenuate Inflammation. Stem cells, https://doi.org/10.1002/stem.2730 (2017).
Chopp, M. & Zhang, Z. Emerging potential of exosomes and noncoding microRNAs for the treatment of neurological injury/diseases. Expert Opin Emerg Drugs 20, 523–526 (2015).
Kim, D.-K. et al. Chromatographically isolated CD63+CD81+ extracellular vesicles from mesenchymal stromal cells rescue cognitive impairments after TBI. Proc Natl Acad Sci USA 113, 170–175, https://doi.org/10.1073/pnas.1522297113 (2016).
Zhang, Y. et al. Systemic administration of cell-free exosomes generated by human bone marrow derived mesenchymal stem cells cultured under 2D and 3D conditions improves functional recovery in rats after traumatic brain injury. Neurochemistry international, https://doi.org/10.1016/j.neuint.2016.08.003 (2016).
Zhang, Y. et al. Effect of exosomes derived from multipluripotent mesenchymal stromal cells on functional recovery and neurovascular plasticity in rats after traumatic brain injury. J Neurosurg 122, 856–867, https://doi.org/10.3171/2014.11.JNS14770 (2015).
Sekiya, I. et al. Expansion of human adult stem cells from bone marrow stroma: conditions that maximize the yields of early progenitors and evaluate their quality. Stem cells (Dayton, Ohio) 20, 530–541, https://doi.org/10.1634/stemcells.20-6-530 (2002).
Kota, D. J. et al. Prostaglandin E2 Indicates Therapeutic Efficacy of Mesenchymal Stem Cells in Experimental Traumatic Brain Injury. Stem Cells 35, 1416–1430, https://doi.org/10.1002/stem.2603 (2017).
Dominici, M. et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy 8, 315–317, https://doi.org/10.1080/14653240600855905 (2006).
Toledano-Furman, N., Prabhakara, K., Bedi, S., Cox, C. J. & Olson, S. OMIP-041: Optimized multicolor immunofluorescence panel rat microglial staining protocol. Cytometry A, https://doi.org/10.1002/cyto.a.23267 (2017).
Dulin, J., Karoly, E., Wang, Y., Strobel, H. & Grill, R. Licofelone modulates neuroinflammation and attenuates mechanical hypersensitivity in the chronic phase of spinal cord injury. J Neurosci 33, 652–664 (2013).
Basso, D. M., Beattie, M. & Bresnahan, J. A sensitive and reliable locomotor rating scale for open field testing in rats. J Neurotrauma 12, 1–21 (1995).
Chaplan, S., Bach, F., Pogrel, J., Chung, J. & Yaksh, T. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 53, 55–63 (1994).
Dixon, W. Efficient analysis of experimental observations. Annu Rev Pharmacol Toxicol 20, 441–462 (1980).
Scheff, S., Rabchevsky, A., Fugaccia, I., Main, J. & Lumpp, J. J. Experimental modeling of spinal cord injury: characterization of a force-defined injury device. J Neurotrauma 20, 179–193 (2003).
Faul, F., Erdfelder, E., Lang, A. G. & Buchner, A. G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behavior Research Methods 39, 175–191 (2007).
Walters, E. Neuroinflammatory contributions to pain after SCI: roles for central glial mechanisms and nociceptor-mediated host defense. Exp Neurol 258, 48–61 (2014).
Alexander, J. & Popovich, P. Neuroinflammation in spinal cord injury: therapeutic targets for neuroprotection and regeneration. Prog Brain Res 175, 125–137 (2009).
Prasanna, S., Gopalakrishnan, D., Shankar, S. & Vasandan, A. Pro-inflammatory cytokines, IFNgamma and TNFalpha, influence immune properties of human bone marrow and Wharton jelly mesenchymal stem cells differentially. PLoS One 5, e9016 (2010).
Saiwai, H. et al. Ly6C+ Ly6G− Myeloid-derived suppressor cells play a critical role in the resolution of acute inflammation and the subsequent tissue repair process after spinal cord injury. J Neurochem 125, 74–88 (2013).
Wang, L., Yu, W., Tao, L. & Xu, Q. Myeloid-derived suppressor cells mediate immune suppression in spinal cord injury. J Neuroimmunol 15, 96–102 (2016).
Walker, J., Maier, C. & Pober, J. Cytomegalovirus-infected human endothelial cells can stimulate allogenic CD4+ memory T cells by releasing antigenic exosomes. J Immunol 182, 1548–1559 (2009).
Bin, Z. et al. Mesenchymal stem cells secrete immunologically active exosomes. Stem Cells and Development 23, 1233–1244 (2013).
Argaw, A. T., Gurfein, B. T., Zhang, Y., Zameer, A. & John, G. R. In Proc Natl Acad Sci USA Vol. 106 1977–1982 (2009).
Xin, H. et al. Secondary release of exosomes from astrocytes contributes to the increase in neural plasticity and improvement of functional recovery after stroke in rats treated with exosomes harvested from microRNA 133b-overexpressed multipotent mesenchymal stromal cells. Cell Transplant, https://doi.org/10.3727/096368916X693031 (2016).
Xin, H. et al. Exosome-mediated transfer of miR-133b from multipotent mesenchymal stromal cells to neural cells contributes to neurite outgrowth. Stem Cells 30, 1556–1564, https://doi.org/10.1002/stem.1129 (2012).
Huang, J. et al. Systemic administration of exosomes released from mesenchymal stromal cells attenuates apoptosis, inflammation and promotes angiogenesis after contusion spinal cord injury in rats. J of Neurotrauma, https://doi.org/10.1089/neu.2017.5063 (2017).
Figley, S., Khosravi, R., Legasto, J., Tseng, Y. & Fehlings, M. Characterization of vascular disruption and blood-spinal cord barrier permeability following traumatic spinal cord injury. J Neurotrauma 31, 541–552 (2014).
Taoka, Y. et al. Role of neutrophils in spinal cord injury in the rat. Neuroscience 79, 1177–1182 (1997).
Donnelly, D. & Popovich, P. G. Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury. Exp Neurol 209, 378–388 (2008).
Lai, C., Tannous, B. & Breakefield, X. Noninvasive in vivo monitoring of extracellular vesicles. Methods Mol Biol 1098, 249–258 (2014).
Grange, C. et al. Biodistribution of mesenchymal stem cell-derived extracellular vesicles in a model of acute kidney injury monitored by optical imaging. Int J Mol Med 33, 1055–1063 (2014).
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Ruppert, K.A., Nguyen, T.T., Prabhakara, K.S. et al. Human Mesenchymal Stromal Cell-Derived Extracellular Vesicles Modify Microglial Response and Improve Clinical Outcomes in Experimental Spinal Cord Injury. Sci Rep 8, 480 (2018). https://doi.org/10.1038/s41598-017-18867-w
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