Transplantation of human bone marrow mesenchymal stromal cells reduces liver fibrosis more effectively than Wharton’s jelly mesenchymal stromal cells
Stem Cell Research & Therapy volume 8, Article number: 143 (2017)
Mesenchymal stromal cells (MSCs) from various tissues have shown moderate therapeutic efficacy in reversing liver fibrosis in preclinical models. Here, we compared the relative therapeutic potential of pooled, adult human bone marrow (BM)- and neonatal Wharton’s jelly (WJ)-derived MSCs to treat CCl4-induced liver fibrosis in rats.
Sprague-Dawley rats were injected with CCl4 for 8 weeks to induce irreversible liver fibrosis. Ex-vivo expanded, pooled human MSCs obtained from BM and WJ were intravenously administered into rats with liver fibrosis at a dose of 10 × 106 cells/animal. Sham control and vehicle-treated animals served as negative and disease controls, respectively. The animals were sacrificed at 30 and 70 days after cell transplantation and hepatic-hydroxyproline content, histopathological, and immunohistochemical analyses were performed.
BM-MSCs treatment showed a marked reduction in liver fibrosis as determined by Masson’s trichrome and Sirius red staining as compared to those treated with the vehicle. Furthermore, hepatic-hydroxyproline content and percentage collagen proportionate area were found to be significantly lower in the BM-MSCs-treated group. In contrast, WJ-MSCs treatment showed less reduction of fibrosis at both time points. Immunohistochemical analysis of BM-MSCs-treated liver samples showed a reduction in α-SMA+ myofibroblasts and increased number of EpCAM+ hepatic progenitor cells, along with Ki-67+ and human matrix metalloprotease-1+ (MMP-1+) cells as compared to WJ-MSCs-treated rat livers.
Our findings suggest that BM-MSCs are more effective than WJ-MSCs in treating liver fibrosis in a CCl4-induced model in rats. The superior therapeutic activity of BM-MSCs may be attributed to their expression of certain MMPs and angiogenic factors.
Liver fibrosis/cirrhosis is a major health problem worldwide and, among the 1.4 million liver disease deaths occurring each year, 55% of these are attributed to liver cirrhosis [1, 2]. Liver fibrosis/cirrhosis-related mortality has been steadily increasing worldwide, as has alcohol consumption, and the prevalence of hepatitis B, C, and diabetes . It has been reported that almost one-fifth (18.3%) of global liver fibrosis/cirrhosis deaths occur in India . Currently, there is no effective treatment available to cure liver fibrosis/cirrhosis. Liver transplantation remains the only option but this is hindered by a lack of donor organs and immune-rejection. Transplantation of adult hepatocytes is another alternative and has been used in clinical studies, predominantly in hereditary metabolic disorders [4, 5] or as a bridging therapy for patients awaiting liver transplantation . Again, a major limitation for broader use of hepatocyte transplantation is the lack of availability of sufficient numbers of primary human hepatocytes.
Understandably, there is a critical need to find an effective alternative therapy for this serious life-threatening disease. Stem cell-based therapy has been considered a potential alternative to liver transplantation. The encouraging advances in stem cell research have provided hope that these cells could be used for the treatment of the end-stage chronic liver diseases. Among various types of stem cells, mesenchymal stromal cells (MSCs) are the preferred cell type due to their easy isolation, high expandability, multilineage differentiation potential, and paracrine activity . Not only can they differentiate into mesodermal lineage but they also have the ability to differentiate into hepatocyte-like cells in vitro and in vivo [8, 9]. MSCs secrete a broad spectrum of growth factors such as hepatocyte growth factor (HGF), vascular endothelial growth factor (VEGF), nerve growth factor (NGF), angiopoetin-1 (Ang-1), insulin-like growth factor (IGF-1) and fibroblast growth factor (FGF-2). Among them HGF, NGF, and VEGF have been identified as important growth factors involved in the regenerative process via antifibrotic, antiapoptotic, progenitor cell proliferation, and neoangiogenesis effects . MSCs have immunosuppressive and anti-inflammatory properties such as inhibitory effects on dendritic cells, natural killer (NK) cells, Th1 cell proliferation, and activation of M2 macrophages and Th2 cells. These effects are mediated via production of prostaglandin E2 (PGE2), indoleamine 2,3-dioxygenase (IDO), nitric oxide (NO), and secretion of anti-inflammatory interleukins such as IL-10 [11,12,13]. These characteristics make MSCs a potential candidate for treating end-stage liver diseases.
Several human clinical trials have been performed using various types of MSCs through different routes of delivery to see the improvement in clinical end-points of liver function in patient with liver fibrosis/cirrhosis and liver failure . Infusion of autologous bone marrow (BM)-derived MSCs (BM-MSCs) through intrahepatic artery delivery  showed improvements in liver biochemical parameters and in histological evaluation of fibrosis. Recently, the beneficial effect of allogeneic umbilical cord (UC)-derived MSCs and BM-MSCs through peripheral vein infusion in patients with liver cirrhosis has been shown . The authors demonstrated improvement in liver function parameters such as total bilirubin, serum albumin, and liver enzymes, as well as model for end-stage liver disease (MELD) score, though all the parameters were not found to be significant. These studies indicate that stem cells including allogeneic MSCs derived from different tissues may provide clinical benefit to these patients, although larger clinical trials with higher numbers of subjects is warranted.
MSCs derived from various tissue sources such as bone marrow, Wharton’s jelly (WJ), adipose tissue, umbilical cord blood, and placenta have been tested in various preclinical models of fibrosis . Among these, BM-MSCs and WJ-MSCs have been thoroughly characterized for their phenotypic expression, cytokine secretion, and immunomodulatory properties. In addition, their antifibrotic activity has been shown in various in vitro and in vivo models [18, 19]. However, the most efficacious tissue source of MSCs for the treatment of liver fibrosis/cirrhosis has not been identified. In this manuscript, we investigated various properties of pooled populations of adult human BM-MSCs and neonatal human WJ-MSCs that may play a critical role in treating liver fibrosis. We observed certain key differences between the two cell types with regards to their angiogenic factor(s) secretion, matrix metalloprotease (MMP) expression, and ability for collagen degradation in vitro. These differences led us to determine the relative therapeutic potential of BM-MSCs and WJ-MSCs in a CCl4-induced preclinical model of liver fibrosis in rats.
Isolation and expansion of BM-MSCs and WJ-MSCs
Bone marrow mononuclear cells (BMMNCs) from three independent donor aspirations, obtained after appropriate informed consent, were separated by the Ficoll density gradient method (1.077 g/ml density). BMMNCs accumulated at the Ficoll-plasma interphase were isolated by carefully aspirating the buffy coat. The buffy layer was then transferred into a fresh 50-ml centrifuge tube, to which an equal volume of culture medium was added, and centrifuged at 1200 rpm for 10 min. The resulting pellet was resuspended with culture medium comprising of 10 ml KO-DMEM (Gibco), 10% fetal bovine serum (FBS; Hyclone), 100 U/ml penicillin (Gibco), 100 μg/ml streptomycin, and 2 mM GlutaMAX™ (Gibco) and gently mixed to obtain a single cell suspension. To 18 ml of freshly prepared complete culture medium in a T75 flask, 2 ml of MNC suspension was added, transferred to a 5% CO2 incubator, and left undisturbed for 48 h. After 48 h, the culture flasks were screened for adherent cells and the nonadherent cells were removed carefully. The cultures were supplemented with 15 ml of fresh medium per flask and the flasks were returned to the CO2 incubator. The medium was replenished every 48 to 72 h. Cells were cultured until they achieved 70-80% confluency. Subsequently, BM-MSCs from the three donors were pooled in equal proportions and expanded in culture. The cells were seeded at a density of 1000 cells/cm2, supplemented with 2 ng/ml recombinant human basic fibroblast growth factor (bFGF; Sigma-Aldrich) from passage 2 (P2) onwards, and expanded in 10 CellSTACK up to P5 as described previously [20, 21]. The cells from P5 were used for further in vitro and in vivo experiments in this study.
For WJ-MSC isolation and expansion, fresh umbilical cords were collected from full-term births after obtaining written informed consent following approval of the ethics committee. After a brief rinse with normal saline (0.9% w/v, sodium chloride), cords were given a quick rinse in 70% isopropanol followed by three washes using sterile DPBS (Gibco). The umbilical cord vein and arteries were removed, and the exposed mesenchymal tissue was cut into small pieces of 1–2 mm before placing them in the tissue culture dish . The explants were cultured in KO-DMEM (Gibco), 10% FBS (Hyclone), 100 U/ml Penicillin (Gibco), 100 μg/ml streptomycin, and 2 mM GlutaMAX™ (Gibco). The MSCs obtained from individual cords were expanded up to P2 using an initial seeding density of 3000 cells/cm2 as standardized and reported in our earlier publication . Cells obtained from three individual cords were pooled at P3, when 2 ng/ml bFGF (Sigma-Aldrich) was introduced into the culture medium. The cells were further expanded in culture medium with 2 ng/ml bFGF up to P6. The WJ-MSCs harvested at P6 were used for further in vitro and in vivo experiments in this study.
Characterization of BM-MSCs and WJ-MSCs
Both BM-MSCs and WJ-MSCs were harvested at 80–90% confluence and resuspended in DPBS at a cell density of 1 × 106 cells/ml. The following marker expressions were analyzed for MSC identification: CD73 (PE), CD90 (PE), and CD105 (PE). To rule out the presence of hematopoietic cells, we used CD14 (FITC), CD19 (FITC), CD34 (FITC), CD45 (FITC), and HLA-DR (FITC) (BD Pharmingen, San Diego, USA) antibodies. FITC- or PE-conjugated mouse IgGs (BD Pharmingen, San Diego, USA) were used as isotype controls. The fluorescence intensity of MSCs was analyzed by flow cytometry (Guava easyCyte™ flow cytometers, Millipore, CA, USA). The adipogenic, osteogenic, and chondrogenic differentiation ability of BM-MSCs and WJ-MSCs was also evaluated according to a procedure described earlier [21,22,23].
Comparative molecular analysis of pooled BM-MSCs and WJ-MSCs
Total cellular RNA was isolated using an RNeasy mini kit (Qiagen). The RNA samples were treated with DNase I (Ambion) and reverse-transcribed into cDNA using a high-capacity cDNA reverse transcription kit (Applied Biosystems) according to the manufacturer’s instructions. The cDNAs were amplified by using gene specific primers as shown in Table 1. A reverse transcriptase negative blank of each sample and a no-template blank served as negative controls. Gene expression was normalized to the housekeeping gene β-actin. Human VEGF, human HGF, and transforming growth factor (TGF)-β in the conditioned medium (CM) were estimated using enzyme-linked immunosorbent assay (ELISA) kits (R&D Systems) according to the manufacturer’s instructions.
Inhibition of hepatic stellate cells activation
Hepatic stellate cells (HSCs; LX-2 line, Cat. No. SCC064, Millipore) were seeded at a density of 3000 cells/cm2. At 50% confluence, the cells were activated with 2% FBS (in KO-DMEM) medium containing 10 ng/ml human TGFβ-1 (Cat. No. 100-21, Peprotech) for 48 h. Next, the medium was replaced with conditioned medium (CM) of BM-MSCs or WJ-MSCs, and diluted to 50% in serum-free medium. The HSCs were incubated for 72 h and processed further for collagen estimation using the Sircol™ Soluble Collagen Assay kit (Cat. No. S1000, Biocolor), as per the manufacturer’s instructions. The HSCs were also plated in chamber slides and tested for the expression of α-smooth muscle actin (SMA) by immunofluorescence assay. Fluorescent images were captured using a Nikon-Eclipse-90i microscope (Nikon) and Image-Pro AMS version 6.0 software.
In this study, male Sprague-Dawley rats were obtained from Harlan laboratories (Indianapolis, Indiana, USA). Rats were maintained in a controlled environment at 22 ± 3 °C temperature, 50 ± 20% humidity, and a light/dark cycle of 12 h each. The experimental protocol was approved by the Institutional Animal Ethics Committee (IAEC) of Syngene International animal facility (Syngene/IAEC/511/06-2014) and the experiments were conducted in the same facility.
Establishment of the CCl4-induced liver fibrosis model
Among the various types of experimental liver fibrosis/cirrhosis models, CCl4-induced method appears to be the most widely applied [24, 25]. In this experiment, liver fibrosis/early cirrhosis was induced in Sprague-Dawley rats by intraperitoneal injection of CCl4 as published by Issa et al.  with slight modifications after internal validation. CCl4 was administered at a dose of 2 ml/kg body weight (CCl4:olive oil = 1:1) twice weekly for an initial 2 weeks, followed by 1 ml/kg body weight twice weekly for the next 6 weeks (Fig. 1). After 48 h from the last CCl4 injection, blood was collected, and the serum was separated and analyzed for aspartate transaminase, alanine transaminase, and total bilirubin by an automated analyzer (EM-360, Erba Mannheim, Germany) according to the manufacturer’s instructions. Based on the results of the alanine transaminase, aspartate transaminase, and total bilirubin analysis, animals were randomly assigned into three groups: vehicle control (n = 12) and BM-MSCs (n = 12) and WJ-MSCs (n = 9) treatment groups. Rats that had not been treated with CCl4 (n = 11) served as normal controls.
Cryopreserved pooled human BM-MSCs or WJ-MSCs were thawed at 37 °C in a water bath, centrifuged, and the pellet was resuspended in PlasmaLyte A (vehicle) at a dose of 10 × 106 BM-MSCs or WJ-MSCs in 0.5 ml vehicle solution. The cells were administered through the tail vein at an infusion rate of 150 μl/min. A separate group of rats received only vehicle (0.5 ml) which served as a control. Rats were sacrificed at days 30 and 70 after cell treatment using CO2 asphyxiation. On day 30, rats from the vehicle (n = 5), BM-MSCs (n = 5) and WJ-MSCs (n = 4) treatment groups were sacrificed. The remaining rats were sacrificed at day 70. During necropsy, samples of liver tissues were collected for liver hydroxyproline content analysis, and histopathological and immunohistochemistry evaluation.
CM-DiI labeling of BM-MSCs and WJ-MSCs
The BM-MSCs or WJ-MSCs were labeled using CM-DiI fluorescent dye (Invitrogen) in order to track them in vivo in rats. Briefly, the cells were resuspended in KO-DMEM (Gibco) along with 5 μM CM-DiI and incubated for 30 min at 37 °C. The excess dye was removed by washing with DPBS, and the cells were resuspended in Plasmalyte A and injected at a dose of 10 × 106 cells/rat through the tail vein. Animals received vehicle alone to serve as normal controls. The DiI-labeled cells were confirmed ex vivo in liver tissues by fluorescence microscopy after 30 days of cell administration.
Quantitative analysis of hepatic hydroxyproline content
The liver hydroxyproline content was quantitated using a hydroxyproline assay kit (QuickZyme Biosciences, Leiden, Netherlands) according to the manufacturer’s instructions. Briefly, the liver tissue (100 mg) was homogenized in 1.5 mL distilled water containing protease inhibitors. Tissue samples were then hydrolyzed at 110 °C for 16 h for oxidation of free hydroxyproline. The hydroxyproline content was assessed by spectrophotometry (Thermo Scientific) at 570 nm.
Liver specimens collected in 10% neutral buffered formalin (NBF) were processed, embedded in paraffin, sectioned (5 μm thick), and stained with hematoxylin and eosin (H&E), Masson’s trichrome (MTC), and Picrosirius red (PSR) for histological examination. The degree of hepatic fibrosis was assessed according to the Ishak modified scoring system .
Morphometric analysis was performed using digitally captured serial images (n = 5) of Sirius red stained sections using Leica software, and the collagen stained area was calculated in a blinded manner.
Immunohistochemical analysis of liver tissues
Immunohistochemical studies were performed on paraffin-embedded liver tissue sections (5 μm thickness) using rat α-SMA antibody (1:1000; Sigma-Aldrich, cat. no. A5228), rat Ki-67 antibody (5 μg/ml; Abcam, cat. no. ab15580), rat EpCAM antibody (1:160; Abcam, cat. no. ab71916), human MMP1 antibody (1:100; Abcam, cat. no. ab52631), and HRP-conjugated secondary antibodies (GBI labs, cat no. D39-18). The immunoreactive product was visualized by adding substrate-chromogen diaminobenzidine (DAB) and counterstained by Mayer’s hematoxylin solution. Stained slides were analyzed by light microscopy (Olympus BX51, Tokyo, Japan).
Immunofluorescence analysis of liver tissues
For immunofluorescence analysis, 5-μm thicknesses of OCT frozen tissue sections were fixed in 4% paraformaldehyde and stained with mouse anti-human CD105 antibody (1:25; BD Pharmingen, cat. no. 555690) followed by a secondary goat anti-mouse FITC antibody (Abcam, cat. no. ab6785). All sections were washed three times and costained with a 1:2000 solution of DAPI (Invitrogen). The DiI/CD105+ cells were visualized and enumerated in five random areas under a fluorescence microscope.
The data were expressed as mean ± SEM. For the comparison of different treatment groups, the data was analyzed by one-way analysis of variance (ANOVA) followed by Dunnett’s multiple comparison test. The histopathological parameters were analyzed using the Kruskal-Wallis test. The results were considered statistically significant at p < 0.05.
Characterization of pooled BM-MSCs and WJ-MSCs
Both BM-MSCs and WJ-MSCs showed the plastic adherence properties and spindle-shaped morphology which are the primary characteristics of MSCs (Fig. 2a). Flow cytometric analysis revealed that these cells expressed CD73, CD90, and CD105 markers and were negative for the hematopoietic markers CD14, CD19, CD34, and CD45. Both BM-MSCs and WJ-MSCs lacked the expression of HLA-DR (Fig. 2b). The adipogenic, osteogenic, and chondrogenic differentiation of BM-MSCs and WJ-MSCs have been published earlier by us [21, 23].
Comparative molecular analysis of BM-MSCs and WJ-MSCs
The gene expression of MMP1, MMP2, MMP13, MMP15, and MMP16 were observed to be higher in BM-MSCs as compared to the WJ-MSCs. Both cell types exhibited expression of MMP3, MMP7, and MMP8. A higher expression of MMP9 was observed in the WJ-MSCs compared to BM-MSCs, whereas none of the cell types expressed MMP12 or MMP24 genes (Fig. 3a). The secretion of VEGF was only observed with BM-MSCs culture (3.9 ± 0.03 ng/ml/million cells), whereas the WJ-MSCs secreted higher amounts of HGF (73.8 ± 0.03 pg/ml/million cells) (Fig. 3b and c). In addition, we observed that TGF-β1 expression was significantly higher in WJ-MSCs than BM-MSCs (data not shown).
Effect of BM-MSCs and WJ-MSCs conditioned media on activated HSCs
The expression of α-SMA in HSCs was analyzed by immunocytochemistry which is a quantitative measure of hepatic fibrosis and could be related directly to liver fibrogenesis and indirectly to human liver fibrosis in chronic liver disease. BM-MSCs-CM treatment showed a marked reduction in the α-SMA-positive cells as compared to WJ-MSCs-CM-treated HSCs (Fig. 4a). To determine the effect of both BM-MSCs and WJ-MSCs on collagen synthesis by activated HSCs, conditioned media obtained from both cell types were tested on activated HSCs. As shown in Fig. 4b, BM-MSCs-CM treatment resulted in a significant reduction in collagen synthesis by the activated HSCs compared to the WJ-MSCs-CM-treated cells. These data suggest that BM-MSCs secrete factors necessary to inhibit HSCs activation and collagen deposition in vitro.
Differential intrahepatic engraftment of DiI-labeled BM-MSCs and WJ-MSCs in the CCl4 animal model
A total of sixteen intraperitoneal injections of CCl4 were given to Sprague-Dawley rats to develop the liver fibrosis model. For the first 2 weeks, an intraperitoneal injection of CCl4 at a dose of 2 ml/kg body weight was given twice weekly followed by 1 ml/kg body weight for an additional 6 weeks (twice weekly) to establish extensive liver fibrosis in Sprague-Dawley rats.
To determine the intrahepatic distribution of BM-MSCs or WJ-MSCs, animals injected with CM-DiI-labeled cells were sacrificed 30 days after cell injection. The number of DiI/CD105+ cells were identified in the liver section and counted in five random fields from each slide under 40× magnification. The results indicated that the number of DiI/CD105+ cells were higher in BM-MSCs-treated animals (1.8 ± 0.84) than WJ-MSC-treated animals (0.8 ± 1.09). The purpose of costaining the MSCs with human CD105 along with DiI was to rule out the possibility of capturing false signals resulting from dead human cells phagocytosed by rat macrophages. These findings suggest that a greater number of intravenously injected BM-MSCs survived and sporadically colonized in the liver in comparison to WJ-MSCs (Fig. 5).
Effect of intravenously injected BM-MSCs and WJ-MSCs on hepatic hydroxyproline content
As expected, the hydroxyproline levels in the liver samples of vehicle-treated animals were significantly higher than normal controls (Fig. 6c). Intravenous administration of BM-MSCs significantly reduced the hepatic hydroxyproline level both at day 30 (p < 0.01) as well as at day 70 (p < 0.05). Hydroxyproline levels were also reduced in WJ-MSC-treated animals; however, the magnitude of reduction was not significant as compared to vehicle-treated animals. These results further substantiated that BM-MSCs were more effective in reducing liver fibrosis than WJ-MSCs.
Effect of BM-MSCs and WJ-MSCs on gross and microscopic liver histopathology
In comparison to normal control rats, the livers of vehicle-treated rats were enlarged, coarser, nodular on the surface, and liver lobes were fused with each other and to the peritoneal organs (Fig. 6a and b) at days 30 and 70. In contrast, rats treated with BM-MSCs showed less coarse surface at day 30 and became reddish, smoother, and lustrous at day 70 (Fig. 6b). Rats treated with WJ-MSCs showed marginal improvement. Histopathological analysis revealed that the Masson’s trichrome- and Picrosirius red-stained collagen fiber area was reduced in BM-MSCs- and WJ-MSCs-treated animals; however, the former population exhibited distinctly enhanced reduction in collagen fiber area compared to either the WJ-MSCs- or vehicle-treated sample. Furthermore, we quantified the Picrosirius red-stained area to analyze the collagen proportionate area. The percentage of collagen proportionate area was significantly reduced in BM-MSCs -treated animals as compared to vehicle-treated animals on day 30 (p < 0.01) and day 70 (p < 0.05). There was no significant reduction observed in the WJ-MSCs-administered samples (Fig. 6d). Furthermore, analysis of the Ishak fibrosis score showed a statistically significant reduction in mean score in BM-MSCs-treated animals as compared to vehicle-treated animals at both time points (Fig. 6e). Consistent with other data, WJ-MSCs-treated animals did not show such improvement.
Immunohistochemical analysis of liver samples
To evaluate the effect of BM-MSCs and WJ-MSCs on activation of HSCs and myofibroblasts, α-SMA-positive cells were examined in the liver sections of vehicle- and MSCs-treated animals. Immunohistochemical staining of liver sections showed intensely stained α-SMA+ cells along the fibrous septa in the vehicle-treated animals (Fig. 7a and b) and the expression was markedly reduced in BM-MSC-treated animals at both days 30 and 70. Our data indirectly suggested that BM-MSCs reduced HSCs and fibroblast/myofibroblast activation in the liver fibrosis model. To determine whether transplanted MSCs promote hepatocyte proliferation and liver regeneration, the number of Ki-67+ cells were enumerated in five random fields (n = 3). The results showed that the number of Ki-67+ nuclei was highest in BM-MSCs-injected animals, followed by the WJ-MSCs- and vehicle-injected groups at days 30 and 70 (Fig. 7c). Similarly, more number of EpCAM+ cells were observed around the portal and ductal region in BM-MSCs-treated liver samples compared to WJ-MSCs and vehicle-treated groups, suggesting that BM-MSC administration may have induced proliferation of liver progenitor cells. Finally, we also examined the expression of the fibrolysis marker MMP1 and found that the number of human MMP1+ cells were higher in BM-MSCs-treated animals in comparison to those treated with WJ-MSCs. Thus, the results suggest that the BM-MSCs reduce fibrogenesis by secreting fibrolytic metalloproteases such as MMP1 and MMP2 (Fig. 7d).
Liver fibrosis is a complex and dynamic process that is orchestrated by various cell types and growth factors resulting in excessive accumulation of collagen and other extracellular matrix (ECM) proteins eventually leading to liver cirrhosis and hepatic failure. Although antifibrotic treatments are available and are commonly used, they are not very effective because they address a single specific mechanism of disease pathophysiology. Thus, the discovery and combination of new drugs that can target multiple cellular pathways of liver fibrogenesis are required for efficacious treatment.
Cell therapy is intended to treat through a multifactorial effect, and thus provides an ideal alternative to currently available treatments. MSCs are considered to be a potential candidate to ameliorate hepatic fibrosis because of their multiple therapeutic effects. Several in vitro studies have shown that MSCs derived from various sources can differentiate into hepatocyte-like cells when differentiation is induced by HGF and FGF4 . Broadly, therapeutic activity can be attributed to secretion of many growth factors including VEGF and HGF and other cytokines, as well as various types of collagen-degrading MMPs. Immunosuppression and anti-inflammatory properties mediated via secretion of IDO, PGE2, IL10, etc. play an important role in reducing excessive inflammation and apoptosis .
In the current study, the comparative analysis of pooled BM-MSCs and WJ-MSCs was carried out in vitro. We have deciphered one of the mechanisms of action of both cell types in reversing the fibrosis using activated HSCs that are known to produce very high levels of collagen . Our in vitro data suggest that secretome of BM-MSCs is superior in degrading collagen compared to that of WJ-MSCs. Furthermore, when we evaluated the expression of MMPs, BM-MSCs expressed a wide range of MMPs such as MMP1, -2, -13, and -16 that are known to catabolize the fibrotic collagens. In addition, the in vivo data demonstrated that intravenous infusion of BM-MSCs exhibited a greater potential to reduce liver collagen content and improve liver architecture as evidenced by liver hydroxylproline levels, collagen proportionate area, and Ishak score as compared to the WJ-MSCs population. The antifibrotic potential of BM-MSCs and WJ-MSCs has been demonstrated in various preclinical models of liver fibrosis , although no direct comparison between the two cell types has been performed in the same animal model. The comparative in vitro and in vivo efficacy results presented here suggest the BM-MSCs might be more effective due to a broader expression of various MMPs necessary for fibrous collagen degradation.
Growth factors such as VEGF and HGF secreted by MSCs are reported to reduce hepatocyte apoptosis and increase liver regeneration . In the current study, BM-MSCs showed higher levels of VEGF secretion whereas WJ-MSCs secreted higher levels of HGF (Fig. 3b and c). Our data corroborates with earlier findings by Amable et al.  who demonstrated that BM-MSCs had higher potential to secrete VEGF compared to WJ-MSCs and adipose tissue-derived MSCs, and that WJ-MSCs secreted higher amounts of HGF compared to the other two cell types. Our study showed some difference in the MMP expression as compared to those performed by Amable et al. We believe these may be due to the use of different culture conditions such as the addition of bFGF and pooling of MSCs from three independent donors in our study. bFGF is known to regulate the MMP expression [33, 34]. Also, interestingly, it was shown that the migration of MSCs through bone marrow endothelium is regulated by MMP2 [35, 36] which showed higher expression in BM-MSCs. Our in vivo data show higher numbers of Ki-67+ and EpCAM+ cells in BM-MSCs-treated animals when compared to WJ-MSCs-treated animals (Fig. 7). It has been shown that both HGF and VEGF exhibit their antifibrotic effect by inhibiting HSCs activity  and by activating the CXCL9-MMP13 axis , respectively. Though WJ-MSCs secrete higher levels of HGF compared to BM-MSCs, WJ-MSCs showed reduced efficacy in ameliorating liver fibrosis. This suggests that higher amounts of HGF secretion alone is not sufficient to predict the potency of a particular MSC population to reduce CCl4-induced hepatic fibrosis. Immunofluorescence results for DiI/CD105+ cells showed that BM-MSCs persisted for a longer duration in the injured liver compared to WJ-MSCs. It is to be noted that Zhao et al.  demonstrated that intravenously transplanted BM-MSCs engrafted and rescued liver fibrosis more efficiently than intraperitoneal and intrahepatic routes of administration. Our study also confirmed that intravenous administration of BM-MSCs resulted in a marked reduction of liver fibrosis as compared to WJ-MSCs in our CCl4-induced liver fibrosis rat model.
In conclusion, our data suggest that BM-MSCs are superior to WJ-MSCs in ameliorating CCl4-induced liver fibrosis in rats, which may be collectively due to several reasons: the differential capacity to home to the injured liver tissue; difference in paracrine activities; variation in MMP synthesis and secretion; and differences in inhibiting HSCs activation. Whether WJ-MSCs delivered through a different route can be as equally effective as BM-MSCs in treating fibrosis still remains an open question. Obviously, future studies would be required to compare antifibrotic effects of BM-MSCs with those derived from other tissues before selecting a cell-based therapeutic product to treat patients with liver fibrosis/cirrhosis.
Basic fibroblast growth factor
Bone marrow mononuclear cells
- CCl4 :
Epithelial cell adhesion molecule
Fetal bovine serum
Fibroblast growth factor
Hepatocyte growth factor
Hepatic stellate cell
Mesenchymal stromal cells
Nerve growth factor
Smooth muscle actin
Transforming growth factor
Vascular endothelial growth factor
Poynard T, Yuen MF, Ratziu V, et al. Viral hepatitis C. Lancet. 2003;362:2095–100.
Bataller R, Brenner D. Liver fibrosis. J Clin Invest. 2005;115:209–18.
Mokdad AA, Alan DL, Saied S, et al. Liver cirrhosis mortality in 187 countries between 1980 and 2010: a systematic analysis. BMC Med. 2014;12:145.
Fox IJ, Chowdhury JR, Kaufman SS, et al. Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation. N Engl J Med. 1998;338(20):1422–6.
Muraca M, Gerunda G, Neri D, et al. Hepatocyte transplantation as a treatment for glycogen storage disease type 1a. Lancet. 2002;359(9303):317–8.
Strom SC, Fisher RA, Thompson MT, et al. Hepatocyte transplantation as a bridge to orthotopic liver transplantation in terminal liver failure. Transplantation. 1997;63(4):559–69.
Pittenger MF, Mackay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284(5411):143–7.
Lee KD, Kuo TK, Whang-Peng J, et al. In-vitro differentiation of human mesenchymal stem cells. Hepatology. 2004;40(6):1275–84.
Fang B, Shi M, Liao L, et al. Systemic infusion of FLK1+ mesenchymal stem cells ameliorate carbon tetrachloride-induced liver fibrosis in mice. Transplantation. 2004;78(1):83–8.
Kinnaird T, Stabile E, Burnett MS, et al. Local delivery of marrow-derived stromal cells augments collateral perfusion through paracrine mechanisms. Circulation. 2004;109:1543–9.
Aggarwal S, Pittenger MF. Human mesenchymal stem cells modulate allogeneic immune cell responses. Blood. 2005;105(4):1815–22.
Thomas JK, Paul L, Caplan AI, et al. MSC: delivery routes and engraftment, cell-targeting strategies, and immune modulation. Stem Cell International. 2013;2013:1–13.
Caplan AI, Sorrell JM. The MSC curtain that stops the immune system. Immunol Lett. 2015;168(2):136–9.
Eom YW, Kim G, Baik SK. Mesenchymal stem cell therapy for cirrhosis: present and future perspectives. World J Gastroenterol. 2015;21(36):10253–61.
Jang YO, Kim YJ, Baik SK, Kim MY, Eom YW, Cho MY, Park HJ, Park SY, Kim BR, Kim JW, Soo Kim H, Kwon SO, Choi EH, Kim YM. Histological improvement following administration of autologous bone marrow-derived mesenchymal stem cells for alcoholic cirrhosis: a pilot study. Liver Int. 2014;34:33–41.
Liang J, Zhang H, Zhao C, Wang D, Ma X, Zhao S, Wang S, Niu L, Sun L.Effects of allogeneic mesenchymal stem cell transplantation in the treatment of liver cirrhosis caused by autoimmune diseases. Int J Rheum Dis. 2017. doi:10.1111/1756-185X13015. [Epub ahead of print].
Esrefoglu M. Role of stem cells in repair of liver injury: experimental and clinical benefit of transferred stem cells on liver failure. World J Gastroenterol. 2013;19(40):6757–73.
Lin SZ, Chang YJ, Liu JW, et al. Transplantation of human Wharton’s jelly-derived stem cells alleviates chemically induced liver fibrosis in rats. Cell Transplant. 2010;19(11):1451–63.
Sakaida I, Terai S, Yamamoto N, et al. Transplantation of bone marrow cells reduces CCl4-induced liver fibrosis in mice. Hepatology. 2004;40(6):1304–11.
Pal R, Hanwate M, Jan M, Totey S. Phenotypic and functional comparison of optimum culture conditions for upscaling of bone marrow-derived mesenchymal stem cells. J Tissue Eng Regen Med. 2009;3(3):163–74.
Mamidi MK, Nathan KG, Singh G, et al. Comparative cellular and molecular analyses of pooled bone marrow multipotent mesenchymal stromal cells during continuous passaging and after successive cryopreservation. J Cell Biochem. 2012;113(10):3153–64.
Swamynathan P, Venugopal P, Kannan S, Thej C, Kolkundar U, Bhagwat S, Ta M, Majumdar AS, Balasubramanian S. Are serum-free and xeno-free culture conditions ideal for large scale clinical grade expansion of Wharton’s jelly derived mesenchymal stem cells? A comparative study. Stem Cell Res Ther. 2014;5(4):88.
Nekanti U, Mohanty L, Venugopal P, et al. Optimization and scale-up of Wharton’s jelly-derived mesenchymal stem cells for clinical applications. Stem Cell Res. 2010;5(3):244–54.
Issa R, Zhou X, Constandinou CM, et al. Spontaneous recovery from micronodular cirrhosis: evidence for incomplete resolution associated with matrix cross-linking. Gastroenterology. 2004;126(7):1795–808.
Constandinou C, Henderson N, Iredale JP. Modeling liver fibrosis in rodents. Methods Mol Med. 2005;117:237–50.
Ishak K, Baptista A, Bianchi L, et al. Histological grading and staging of chronic hepatitis. J Hepatol. 1995;22(6):696–9.
Kang XQ, Zang WJ, Bao LJ, et al. Fibroblast growth factor-4 and hepatocyte growth factor induce differentiation of human umbilical cord blood-derived mesenchymal stem cells into hepatocytes. World J Gastroenterol. 2005;11(47):7461–5.
Usunier B, Benderitter M, Tamarat R, et al. Management of fibrosis: the mesenchymal stromal cells breakthrough. Stem Cells Int. 2014;2014:340257.
Iredale JP, Thompson A, Henderson NC. Extracellular matrix degradation in liver fibrosis: biochemistry and regulation. Biochim Biophys Acta. 2013;1832(7):876–83.
Zhao DC, Lei JX, Chen R, Yu WH, Zhang XM, Li SN, Xiang P. Bone marrow-derived mesenchymal stem cells protect against experimental liver fibrosis in rats. World J Gastroenterol. 2005;11(22):3431–40.
Madrigal M, Rao KS, Riordan NH. A review of therapeutic effects of mesenchymal stem cell secretions and induction of secretory modification by different culture methods. J Transl Med. 2014;12:260.
Amable PR, Teixeira MV, Carias RB, et al. Protein synthesis and secretion in human mesenchymal cells derived from bone marrow, adipose tissue and Wharton’s jelly. Stem Cell Res Ther. 2014;5(2):53.
Eto H, Suga H, Aoi N, Kato H, Doi K, Kuno S, Tabata Y, Yoshimura K. Therapeutic potential of fibroblast growth factor-2 for hypertrophic scars: upregulation of MMP-1 and HGF expression. Lab Invest. 2012;92(2):214–23.
Xie J, Bian H, Qi S, Xu Y, Tang J, Li T, Liu X. Effects of basic fibroblast growth factor on the expression of extracellular matrix and matrix metalloproteinase-1 in wound healing. Clin Exp Dermatol. 2008;33(2):176–82.
De Becker A, Van Hummelen P, Bakkus M, Vande BI, De Wever J, De Waele M, et al. Migration of culture-expanded human mesenchymal stem cells through bone marrow endothelium is regulated by matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-3. Haematologica. 2007;92:440–9.
Bhoopathi P, Chetty C, Gogineni VR, Gujrati M, Dinh DH, Rao JS, et al. MMP-2 mediates mesenchymal stem cell tropism towards medulloblastoma tumors. Gene Ther. 2011;18:692–701.
Kim MD, Kim SS, Cha HY, et al. Therapeutic effect of hepatocyte growth factor-secreting mesenchymal stem cells in a rat model of liver fibrosis. Exp Mol Med. 2014;46:e110.
Yang L, Kwon J, Popov Y, et al. Vascular endothelial growth factor promotes fibrosis resolution and repair in mice. Gastroenterology. 2014;146(5):1339–50.
Zhao W, Li JJ, Cao DY, et al. Intravenous injection of mesenchymal stem cells is effective in treating liver fibrosis. World J Gastroenterol. 2012;18(10):1048–58.
The authors would like to thank the Director General of Health, Malaysia, for permission to publish this article. We gratefully acknowledge the assistance of Dr. Alan Khoo Soo Beng, Dr Munirah Ahmad, and the staff of the Specific-Pathogen-Free (SPF) Laboratory of IMR for supporting the in vivo experiment. We wish to acknowledge Mr. Pablo Bora (Stempeutics Research Pvt. Ltd., Bangalore) for reviewing the manuscript.
The work was supported by Institute for Medical Research (IMR; NMRR-13-1063-18209), Ministry of Health, Kuala Lumpur, Malaysia, and by Stempeutics Research Pvt. Ltd., Bangalore.
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All data generated or analyzed during this study are included in this published article.
MR and GS: conception and design, collection and/or assembly of data, data analysis and interpretation, manuscript writing; NAF and Siddikuzzaman: collection and/or assembly of data, data analysis and interpretation, manuscript writing; SB: conception and design and/or assembly of data, data analysis and interpretation; PS, CT, and GS: collection and/or assembly of data; PKG: contributed in conceptualizing the study and manuscript editing; AKD: reviewing the manuscript; NAF and AZAR: coordinated and helped in conducting the animal experiments; KSF and LMN: contributed to interpretation of results; ZZ: contributed in conceptualizing the study and manuscript editing; ASM: conception and design, assembly of data, data analysis and interpretation, manuscript writing, and final approval of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
The experimental protocol was approved by the Institutional Animal Ethics Committee (IAEC) (Syngene/IAEC/511/06-2014) of Syngene International animal facility. Animals were maintained at the same facility and all the animal experiments were conducted in the same facility in accordance with the experimental ethics committee.
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Rengasamy, M., Singh, G., Fakharuzi, N.A. et al. Transplantation of human bone marrow mesenchymal stromal cells reduces liver fibrosis more effectively than Wharton’s jelly mesenchymal stromal cells. Stem Cell Res Ther 8, 143 (2017). https://doi.org/10.1186/s13287-017-0595-1