Dysregulation of Mesenchymal Stromal Cell Antioxidant Responses in Progressive Multiple Sclerosis

Abstract
 The potential of autologous cell‐based therapies including those using multipotent mesenchymal stromal cells (MSCs) is being investigated for multiple sclerosis (MS) and other neurological conditions. However, the phenotype of MSC in neurological diseases has not been fully characterized. We have previously shown that MSC isolated from patients with progressive MS (MS‐MSC) have reduced expansion potential, premature senescence, and reduced neuroprotective potential in vitro. In view of the role of antioxidants in ageing and neuroprotection, we examined the antioxidant capacity of MS‐MSC demonstrating that MS‐MSC secretion of antioxidants superoxide dismutase 1 (SOD1) and glutathione S‐transferase P (GSTP) is reduced and correlates negatively with the duration of progressive phase of MS. We confirmed reduced expression of SOD1 and GSTP by MS‐MSC along with reduced activity of SOD and GST and, to examine the antioxidant capacity of MS‐MSC under conditions of nitrosative stress, we established an in vitro cell survival assay using nitric oxide‐induced cell death. MS‐MSC displayed differential susceptibility to nitrosative stress with accelerated senescence and greater decline in expression of SOD1 and GSTP in keeping with reduced expression of master regulators of antioxidant responses nuclear factor erythroid 2‐related factor 2 and peroxisome proliferator‐activated receptor gamma coactivator 1‐α. Our results are compatible with dysregulation of antioxidant responses in MS‐MSC and have significant implications for development of autologous MSC‐based therapies for MS, optimization of which may require that these functional deficits are reversed. Furthermore, improved understanding of the underlying mechanisms may yield novel insights into MS pathophysiology and biomarker identification. Stem Cells Translational Medicine 2018;7:748–758

MS is an inflammatory demyelinating and neurodegenerative disease of the central nervous system, and progressive forms of MS are characterized by a relentless accumulation of neurological disability over time for which effective treatment is a major unmet clinical need. Mesenchymal stromal cells (MSCs) have a range of properties of relevance to cell therapy for MS including anti-inflammatory, immunomodulatory, and antioxidant paracrine activity [14]. Given the wealth of preclinical data demonstrating amelioration of disease and their favorable safety profile, there has been rapid clinical translation of autologous MSC-based cell therapy for MS [15]. However, studies have shown that MSC function changes with age and chronic exposure to a proinflammatory environment [9,16] and few data are available regarding MSC function in MS.
We have recently demonstrated that MSC isolated from patients with progressive MS (MS-MSC) have reduced ex vivo proliferation and clonogenic potential, premature senescence, and accelerated shortening of telomere terminal restriction fragments [17]. We have also shown that the MS-MSC secretome has reduced in vitro neuroprotective potential [18]. Recently, others have demonstrated abnormalities in MSC isolated from patients with progressive supranuclear palsy (PSP) [19]. These findings add to the growing body of literature documenting altered MSC function in disease states, and the role of MSC in their pathogenesis, and/or development of associated comorbidities [20], is now under investigation in a range of clinical contexts including ageing syndromes [21,22], metabolic syndrome [23], diabetes [24,25], rheumatoid arthritis [26], and systemic lupus erythematosus [27].
Given that nitrosative stress has been implicated in the pathogenesis of ageing [10], neurodegeneration [2], and MS [11,12], we sought to examine the antioxidant capacity of MS-MSC and their susceptibility to nitric oxide-induced cell death as determined by exposure to DETANONOate, a nitric oxide donor.

Study Cohort
MSC were isolated with appropriate consent from bone marrow samples from individuals undergoing elective total hip replacement surgery (control MSC [C-MSC]; UK Research Ethics Committee [REC] 10/H102/69) and patients with progressive MS (MS-MSC) participating in the ACTiMuS (Assessment of Bone Marrow-Derived Cellular Therapy in Progressive Multiple Sclerosis, NCT01815632, REC 12/SW/0358) trial [17]. The clinical details of control and MS subjects (sex, age, classification of MS, duration of disease progression, and exposure to disease modifying therapy [DMT]) are presented as Supporting Information (Table S1) together with the inclusion and exclusion criteria for the ACTiMuS trial (Supporting Information Table S2). In summary, patients with either primary or secondary MS with an Expanded Disability Status Scale [28] of 4-6 were eligible for the study if they were systemically well despite a clear history of disease progression in the preceding year during which time they must not have been on DMT for MS.
The control cohort were older; median age of control subjects 58.5 years old (7 males and 7 females) and median age of MS patients 53 years old (13 males and 16 females; unpaired t test p = .003). There was no sex bias between the cohorts (p = .772) and an independent effect attributable to birth sex was not observed in analyses. The control cohort had not been exposed to immunomodulatory therapy in the past. None of the 13 patients with primary progressive MS had been exposed to immunomodulatory therapy or DMT. Of those with secondary progressive MS (n = 16), eight had previously been treated with DMT (50%), and in all cases, treatment had been discontinued >1 year prior to collection of marrow in keeping with the entry criteria for the ACTiMuS trial. Not all samples were available for all experiments; the number of biological replicates is specified in each experiment individually and details regarding the cohort and which samples were used for each analysis are presented as Supporting Information. There was no significant association between age and duration of disease progression in the MS cohort. Although there were insufficient patients with a history of exposure to DMT included in the experiments to perform regression analysis, there was no difference between the cohorts with primary and secondary progressive disease in any of the analyses.

Isolation of Bone Marrow-Derived MSC
MSC from control and MS marrow were isolated using density gradient centrifugation and seeded in 25 cm 2 flasks (passage 0) with medium consisting of low glucose Dulbecco's modified Eagle's medium (DMEM) (Sigma USA) with 10% foetal bovine serum (FBS) selected for the growth of MSC (Gibco USA) and 1% Penicillin and Streptomycin (Sigma). At approximately 70% confluence, plastic-adherent cells were detached using 0.25% trypsin (Sigma) and reseeded at 2.5 × 10 5 cells per 75 cm 2 flask (passage 1). To ensure isolated MSC conformed to international defining criteria [29], cell surface phenotype and mesenchymal differentiation potential were examined as previously reported [30]. For all experiments, both control (C-MSC) and MS-MSC were matched for passage number (either at passage 3 [p3] or passage 4 [p4]) to avoid potentially confounding effects.

Proteomics
Protein was extracted from MSC using mirVana PARIS RNA and protein purification kit (Life Technologies USA), following which samples were incubated on ice for 30 minutes and then centrifuged at 10,000g for 10 minutes. The supernatant was collected and stored at −80 C. Protein content was determined using the Qubit Fluorometer and Quant-iT Protein assay kit (Invitrogen USA) according to manufacturer's instructions and diluted to 2 mg/ml.
Liquid chromatography-tandem mass spectrometry (LC-MSMS) of C-MSC and MS-MSC conditioned medium was performed by the University of Bristol Proteomics Facility using a previously described protocol for tandem mass tagging (Thermo Fisher Scientific USA) coupled to liquid chromatography-mass spectrometry [31]. Values were normalized to a randomly selected control.

Bromodeoxyuridine Cell Proliferation Assay
MSC were seeded at 1 × 10 4 cells per well in a 96 well plate. DETANONOate and bromodeoxyuridine (BrdU) (Millipore UK) were added following cell adherence for 24 hours. Cells were subsequently fixed, washed, and incubated with anti-BrdU monoclonal antibody for 1 hour according to manufacturer's instructions. After the addition of the peroxidase-conjugated secondary antibody, substrate, and stop solution, the OD signal was measured using a spectrophotometer with a wavelength of 450 nm. Immunoblotting MSC (5 × 10 4 cells per well) were cultured in a 6-well plate for 5 days before exposure to 0.6 mM of DETANONOate. At set time points (2, 6, and 24 hours), cells were washed and lysed using universal lysis buffer (Millipore). A Qubit Fluorometer and Quant-iT Protein assay kit (Invitrogen) were used according to manufacturer's instructions to ensure equal loading of samples. Western blot and dot blot analysis were performed as previously described [32]. In brief, protein lysates were denatured at 95 C and run on Tris-HCl 10%-20% ready gels (Bio-Rad) for Western blot or diluted in Tris-buffered saline (TBS, Biorad USA) and added to the Bio-Dot Microfiltration apparatus containing a prewet nitrocellulose membrane (Bio-Rad). After transfer to nitrocellulose membrane and blocking in 5% BSA (Sigma) or 5% of milk in TBS-Tween for 1 hour, membranes were incubated overnight in primary antibody at 4 C. Antibodies used were mouse anti-SOD1 (1:2,000, R&D USA), mouse anti-GSTP1 (1:2,000; Santa Cruz USA), rabbit antiperoxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC1α) (1:3,000; Santa Cruz), rabbit anti-nuclear factor erythroid 2-related factor 2 (Nrf2) (1:3,000; Santa Cruz), rabbit anticatalase (1:5,000; Abcam UK), mouse anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (1:5,000; Abcam), and antiactin (1:5,000; Abcam). Specific protein expression patterns were visualized by chemiluminescence using ECL Plus Western Blotting Detection System (Amersham USA). After developing, the ChemiDoc MP Imager (Biorad), Image Lab software was used to measure the integrated density. Values are expressed relative to loading control proteins GAPDH or actin. Western blots were used to confirm antibody specificity and for baseline comparison of protein expression between C-MSC and MS-MSC. Given the number of replicates over multiple time points, dot blots were used for determination of protein expression in experiments using exposure to DETANONOate.

Real-Time Polymerase Chain Reaction
RNA was extracted and cDNA produced using the Taqman gene expression cells-Ct-kit (Applied Biosystems USA) according to the manufacturer's instructions. RNA samples were quantified using a Quant-iT RNA assay kit (Invitrogen) according to manufacturer's instructions to ensure equal loading. Real-time polymerase chain reaction (RT-PCR) was performed using the StepOnePlus Real-Time PCR System (Applied Biosystems) with Assay-on-demand Gene Expression Products for SOD1, GSTP1, PGC1α, Nrf2, and GAPDH (Taqman MGB probe, FAM dye-labeled, Applied Biosystems) using 10 ng cDNA in 20 μl of FAST master mix (Applied Biosystems). Reactions were run at 50 C for 2 minutes, 95 C for 20 seconds, 40 cycles of 95 C for 1 second, and 60 C for 20 seconds. Samples were analyzed in triplicate. Relative gene expression (relative quantification value) was calculated using the 2 −ΔΔCt method with GAPDH as reference (housekeeping) gene.

SOD and GST Activity Assay
SOD and GST activities were quantified in cell lysates using the relevant colorimetric assay (Abcam) according to manufacturer's protocol. OD was measured at 450 nm for SOD and 340 nm for GST in kinetic mode.

Statistical Analysis
All graphs were generated using GraphPad PRISM 5 (Graph Pad Software USA), which was also used for statistical analyses (*) other than those which used multiple regression (#

Reduced Secretion of SOD1 and GSTP by MS-MSC Associated with Duration of Progressive MS
Using LC-MSMS, SOD1, and GSTP1 were detected in the secretome of C-MSC and MS-MSC but there was a relative reduction in the secretion of both antioxidants by MS-MSC (Fig. 1A,  1D). The results were confirmed using ELISA; an independent negative effect of the presence of progressive MS was seen on secretion of both SOD1 and GSTP1 when the effect of age was taken into consideration (Fig. 1B, 1E). Secretion of both SOD1 and GSTP1 correlated negatively with duration of the progressive phase of MS (Fig. 1C, 1F). Catalase secretion was not detected in the MSC secretome using LC-MSMS.

Reduced Expression of SOD1 and GSTP with Reduced Activity of SOD and GST in MS-MSC
Immunoblotting was used to examine the expression of SOD1 and GSTP1 and demonstrated reduced expression in MS-MSC when adjustment was made for the effect of age ( Fig. 2A, 2B). There was no difference in catalase expression (Fig. 2C), and additional analyses of catalase activity were not therefore undertaken. Antioxidant activity was assessed using activity assays for total SOD and GST attributable to the lack of availability of an assay capable of differentiating between activity of specific isoforms. Accounting for effects of age, MS-MSC had reduced activity of both SOD (Fig. 2E) and GST (Fig. 2F).

MS-MSC have Increased In Vitro Susceptibility to Nitrosative Stress
C-MSC was exposed to DETANONOate at varying concentrations for 24 hours, and cell survival was determined using MTT assay. Based on our previous experience with in vitro assays of cell toxicity and survival, we selected the dose for subsequent cell survival studies as that inducing approximately 33% cell death (0.6 mM DETANONOate inducing 37% cell survival; data not shown). C-MSC and MS-MSC were exposed to 0.6 mM DETANONOate for 24 hours, and the effects on cell survival are compared. MS-MSC displayed increased susceptibility to DETANONOate, an effect sustained statistically when regression analysis was undertaken to account for effect of age (Fig. 3A). No differences in MS-MSC survival were observed according to MS subtype (primary or secondary progressive disease) or duration of progressive phase of the disease.
Despite the short duration of experiments, BrdU was used to exclude the possibility that differences in cell survival between populations of C-MSC and MS-MSC could be explained by altered proliferation rate; no difference in MSC proliferation between MS and control cohorts was noted following exposure of MSC to 6 mM DETANONOate for 24 hours (Fig. 3B).

DETANONOate Induces Accelerated Senescence in MS-MSC
Increasing MSC donor age is known to increase senescence [17], and multiple regression analysis was used in all analyses of SA-β-gal expression. C-MSC and MS-MSC at p4 were treated with 0.6 mM DETANONOate for 24 hours following which the SA-β-gal assay was performed to quantify senescent cells (blue staining). Very low levels of SA-β-gal expression are seen following MSC exposure to MIN alone for 24 hours (Fig. 4A, 4B). As expected, MSC SA-β-gal expression increased following DETANONOate exposure consistent  with an increase in number of senescent MSC (Fig. 4C-4E). Senescent cells displayed expected phenotypical changes including enlarged flattened morphology, granular cytoplasm, vacuoles and enlarged nuclei (Fig. 4C, 4D). Following DETA-NONOate exposure, the proportion of senescent cells as defined by those expressing SA-β-gal was significantly greater in MS-MSC cultures compared with the proportion of senescent C-MSC (Fig. 4E).

Reduced MS-MSC Expression of SOD1 and GSTP1 Following Exposure to Nitrosative Stress
Expression of SOD1 and GSTP1 under conditions of nitrosative stress were examined following exposure of MSC to DETA-NONOate for 24 hours as previously. SOD1 gene expression increased after 24 hours of DETANONOate exposure and no difference in response was seen between C-MSC and MS-MSC (Fig. 5A). However, protein expression of SOD1 declined in both C-MSC and MS-MSC with an earlier and greater decline observed in MS-MSC (Fig. 5B). No significant changes in GSTP1 gene expression were seen at any of the time points examined in C-MSC or MS-MSC (Fig. 5C) although GSTP1 protein expression was lower in MS-MSC at 2 and 6 hours and, adjusting for age, an independent, negative, statistically significant effect of the presence of MS on GSTP1 expression was observed (Fig. 5D).

Reduced Nrf2 Expression in MS-MSC in Standard Culture Conditions and Following Nitrosative Stress
The transcriptional factor Nrf2 is a key regulator of antioxidant-enzyme genes, and we therefore explored (i) whether MS-MSC have reduced expression of Nrf2 under standard culture conditions and (ii) whether Nrf2 expression increases in response to DETANONOate exposure. Western blot analysis under standard culture conditions demonstrated that MS-MSC express lower levels of Nrf2 compared to C-MSC (Fig. 6A). Nrf2 gene expression was upregulated in both C-MSC and MS-MSC over the 24-hour period following exposure to DETANONOate (Fig. 6C). Following exposure of C-MSC to nitrosative stress, Nrf2 protein expression showed a trend toward an increase in expression, particularly after 2 and 6 hours of DETANONOate exposure (Fig. 6D). In contrast, MS-MSC expression of Nrf2 declined over the 24-hour period following exposure to DETANONOate (Fig. 6D).

MS-MSC in Standard Culture Conditions and Following Nitrosative Stress Have Reduced Expression of PGC1α
The master regulator of ROS-detoxifying enzymes PGC1α was measured in MSC from both control subjects and patients with MS under standard culture conditions and after 2, 6, and 24 hours of DETANONOate exposure. Protein expression of PGC1α was significantly decreased in MS-MSC compared to C-MSC under standard culture conditions following adjustment for age (Fig. 7A). At the time points examined after DETA-NONOate treatment (2, 6, and 24 hours), there was no change in PGC1α gene expression in either C-MSC or MS-MSC (Fig. 7C). However, C-MSC and MS-MSC showed differing responses to DETANONOate exposure in the level of PGC1α protein expression with a reduction observed in MS-MSC (Fig. 7D).

DISCUSSION
MSC have been identified as an excellent candidate for cell therapy in a wide variety of clinical contexts. Increasingly, however, attention is being given to the quality of MSC used for therapy, particularly autologous cells which have been exposed to disease microenvironment. Detailed examination of MSC isolated from donors with chronic diseases is yielding novel insights into disease pathophysiology and in vivo MSC function. In this study, we have examined the susceptibility of MS-MSC to nitrosative stress in vitro together with an analysis of We have demonstrated that nitrosative stress differentially affects MS-MSC, inducing changes of accelerated senescence. In basal cell culture conditions and following exposure to nitrosative stress, MS-MSC have reduced levels of expression of Nrf2 and PGC1α known regulators of the antioxidant response. There is concomitant reduced expression of antioxidants SOD1 and GSTP although catalase expression was unaltered. In vitro activity of SOD and GST was both reduced in MS-MSC.
PGC1α has a key role in mitochondrial biogenesis, respiration, and induction of antioxidant programs [33]. Reduced expression in MS has been noted and is thought to contribute to mitochondrial changes and neuronal loss [34]. PGC1α lacks DNA-binding activity but interacts with and coactivates several transcription factors including Nrf2, which controls constitutive and inducible expression of an array of antioxidant enzymes including SOD, GST, and catalase [35]. Downregulation of PGC1α has been shown to affect the antioxidant response in Friedreich's ataxia [36] and expression of PGC1α has been noted to be lower in adipose tissue-derived MSC from elderly donors [37]. Interestingly, MSC isolated from patients with PSP had fivefold lower levels of expression of PGC1α compared with control MSC [19] and, in an induced pluripotent stem cell model of Parkinson's disease, S-nitrosylation of the transcription factor myocyte enhancer factor 2c (MEF2C) contributes to mitochondrial dysfunction and apoptotic cell death via dysregulation of the PGC1α-MEF2C transcriptional network [38], a Nrf2 is a regulator of cellular resistance to oxidative stress with an integral role in controlling expression of antioxidant response element-dependent genes. Nrf2 is known to be  activated by nitrosative agents [39], and its repression has been associated with ageing [35] including in a model of Hutchinson-Gilford progeria syndrome where MSC attrition is accelerated [40]. Nrf2 has been shown to maintain the selfrenewal potential of MSC [41], and overexpression induces MSC proliferation and reduces apoptosis, including in response to oxidative stress [42,43]. In models of MS, loss of Nrf2 has been shown to exacerbate neurological deficits [44,45] with activation being protective [46]. Dimethyl fumarate, a disease modifying agent for the treatment of MS, may act at least in part via activation of the Nrf2 pathway [47,48]. The mechanism(s) underlying reduced expression of Nrf2 in MS-MSC in response to nitrostative stress has not been identified to date. Regulation of Nrf2 is complex and involves multiple pathways but a major factor is known to be the variation in the level of protein stability; under basal conditions, Nrf2 is rapidly degraded by the 26S proteasome, and this allows for an immediate increase when ubiquitylation and proteasomal degradation are inhibited by stimuli including redox stress [49]. Low levels of Nrf2 in the absence of environmental stressors have also been attributed to translational repression [50], suggesting that a possible alternative or additional mechanism for the failure to increase Nrf2 expression in MS-MSC was failure to reverse the translational repression of Nrf2 appropriate for basal conditions. Indeed, we note that in experimental allergic encephalitis as in our experiments, Nrf2 mRNA levels are maintained but expression is reduced suggesting either impaired translation or changes in post-translational processing [51].
We note the differences in age between the control and MS cohorts and have used a multiple regression model to account for this. There was no sex bias in the cohorts, and an independent effect attributable to birth sex was not observed in the regression analyses. In addition to agemismatch between cohorts, an additional potential confounding factor is the difference in MSC source between patients and control subjects, that is, marrow from the posterior iliac crest and femoral head, respectively. However, pelvic marrow is generally taken to be the gold standard for MSC isolation [52] and while the indication for hip replacement in the control cohort could be a possible additional confounding factor, MSC changes in the context of osteoarthritis have not been consistently reported [53][54][55][56]. None of the control subjects or those with primary progressive MS had exposure to immunomodulatory drugs or DMT. We were unable to perform regression analyses to determine if there was an independent effect of prior exposure to DMT in the cohort with secondary progressive MS attributable to the low numbers of patients included in each analysis. However, there was no differential effect of disease subtype on any of the analyses undertaken and this, combined with the time interval between exposure and marrow collection, would make it relatively unlikely that our disease-specific results can be explained by DMT exposure.
Our findings are consistent with a failure of homeostasis in MS-MSC attributable to dysregulation of PGC1α and Nrf2-mediated antioxidant responses, which in turn contribute to a phenotype of premature aging. We note that a similar mechanism has been proposed in the context of vascular oxidative stress associated with ageing [57]. The negative association between antioxidant responses (SOD1 and GSTP1 secretion) and duration of progressive MS raises the possibility that chronic exposure to disease adversely affects MSC function with functional consequences for the bone marrow microenvironment including, for example, alterations in regulatory and pro-inflammatory T-cell populations. While this may, in turn, contribute to disease pathophysiology, the finding adds to our previous work, demonstrating changes consistent with accelerated ageing in MS bone marrow and has clear implications for both MSC-based and autologous haematopoietic stem cell therapy for MS and other conditions where oxidative stress plays a role in disease [17]. It would suggest that bone marrow-derived cell therapy is more likely to be effective in MS patients with a shorter phase of progressive disease although, based on currently available data, we are unable to speculate regarding a cutoff in terms of age or disease duration for consideration of therapy.
Future work will include analyses of expression of additional Nrf2 and PGC1α target genes, examination of vascular oxidative stress associated with MS, exploration of whether reversal of the identified deficits in antioxidant response of MS-MSC improves the neuroprotective potential of MS-MSC, and further analysis of bone marrow microenvironment and function in MS.

CONCLUSION
We have demonstrated that MS-MSC have reduced expression of Nrf2 and PGC1α under basal culture conditions with reduced expression of key antioxidants SODs and GSTP and reduced activity of SOD and GST. Furthermore, MS-MSC have increased susceptibility to nitrosative stress which is associated with reduced expression of Nrf2 and PGC1α. Our findings have significant implication for those developing autologous MSCbased therapies for MS as identification and correction of the factors responsible are likely to be required if the full potential of MSC for autologous cell-based treatment is to be realized. Furthermore, we predict that understanding the mechanisms involved will yield novel insights into the pathophysiology of MS and aid identification of new drug targets for the treatment of progressive MS.

AUTHORS CONTRIBUTION
J.R.: conception and design, collection of data, data analysis and interpretation, manuscript writing, final approval of manuscript; P.S.: provision of study material or patients, final approval of manuscript; K.K.: data analysis and interpretation, final approval of manuscript; K.J.H.: collection of data, final approval of manuscript; A.W.: data analysis interpretation, final approval of manuscript; N.J.S.: conception and design, manuscript writing, final approval of manuscript; C.M.R.: conception and design, data analysis and interpretation, manuscript writing, final approval of manuscript.

DISCLOSURE OF POTENTIAL CONFLICTS OF INTEREST
The authors indicated no potential conflicts of interests.