Potential use of human adipose mesenchymal stromal cells for intervertebral disc regeneration: a preliminary study on biglycan-deficient murine model of chronic disc degeneration
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Biglycan is an important proteoglycan of the extracellular matrix of intervertebral disc (IVD), and its decrease with aging has been correlated with IVD degeneration. Biglycan deficient (Bgn−/0) mice lack this protein and undergo spontaneous IVD degeneration with aging, thus representing a valuable in vivo model for preliminary studies on therapies for human progressive IVD degeneration. The purpose of the present study was to assess the possible beneficial effects of adipose-derived stromal cells (ADSCs) implants in the Bgn−/0 mouse model.
To evaluate ADSC implant efficacy, Bgn−/0 mice were intradiscally (L1-L2) injected with 8x104 ADSCs at 16 months old, when mice exhibit severe and complete IVD degeneration, evident on both 7Tesla Magnetic Resonance Imaging (7TMRI) and histology. Placebo and ADSCs treated Bgn−/0 mice were assessed by 7TMRI analysis up to 12 weeks post-transplantation. Mice were then sacrificed and implanted discs were analyzed by histology and immunohistochemistry for the presence of human cells and for the expression of biglycan and aggrecan in the IVD area.
After in vivo treatment, 7TMRI revealed evident increase in signal intensity within the discs of mice that received ADSCs, while placebo treatment did not show any variation. Ultrastructural analyses demonstrated that human ADSC survival occurred in the injected discs up to 12 weeks after implant. These cells acquired a positive expression for biglycan, and this proteoglycan was specifically localized in human cells. Moreover, ADSC treatment resulted in a significant increase of aggrecan tissue levels.
Overall, this work demonstrates that ADSC implant into degenerated disc of Bgn−/0 mice ameliorates disc damage, promotes new expression of biglycan and increased levels of aggrecan. This suggests a potential benefit of ADSC implant in the treatment of chronic degenerative disc disease and prompts further studies in this field.
KeywordsDisc Degeneration Mesenchymal Stromal Cell Chondrogenic Differentiation Degenerative Disc Disease Disc Regeneration
7-Tesla magnetic resonance imaging
Human-derived adipose mesenchymal stem cell
Dulbecco's modified Eagle's medium
Dulbecco’s phosphate-buffered saline
epidermal growth factor
fluorescence-activated cell sorting
basic fibroblast growth factor 2
fetal bovine serum
magnetic resonance imaging
mesenchymal stem cell
number of averages
rapid acquisition with relaxation enhancement
stem cell medium
small leucine repeat proteoglycans
- T1-wi and T2-wi
T1 and T2-weighted images
The degeneration of the intervertebral disc (IVD) is a physio-pathological process accelerating with age and considered as the major cause of diverse spine disorders. Indeed, IVD degeneration represents the main cause of the low-back pain that affects the majority of the adult population, and causes a huge loss of time from work as well as relevant medical expenses . As demonstrated by Furukawa et al. , the degenerative changes in the IVD that occur in pathologic processes are similar to those associated with normal aging. In addition, IVD degeneration may be premature or early onset of the aging process, or taken as a distinct process from aging .
The IVD is the largest enclosed and avascular tissue of the human body, and possesses a peculiar microenvironment, characterized by high mechanical and osmotic pressures, severe hypoxia, and a very limited supply of nutrients . Its core, called the nucleus pulposus (NP), is composed of a jelly-like material that consists mainly of water, as well as the extracellular matrix (ECM) components, including a loose network of collagen fibers and proteoglycans. This ECM composition is similar to the articular cartilage, as it contains several members of the small leucine repeat proteoglycans (SLRPs) family . Temporal and spatial expressions of some SLRPs, in particular biglycan, have been demonstrated in the human IVD - and their decreasing level appears to correlate with age and degeneration of human IVD . IVD degeneration has been found to spontaneously occur in biglycan-deficient (Bgn −/0 ) mice, which therefore represent a valuable in vivo model to study degenerative disc disease . In this animal model, 7-Tesla magnetic resonance imaging (7TMRI) is a noninvasive tool that is able to evaluate pathological evolution over time and therapeutic follow up .
Different therapies have been proposed for the treatment of IVD degeneration, and among them, the use of cell therapy strategies to supplement/replenish the cell population in IVD degeneration appears promising -. For example, rabbit annulus fibrosus (AF) cells cultured in an atelocollagen honeycomb-shaped scaffold have been allografted into the lacunae of NP of rabbit IVD to treat degeneration through a tissue-engineering method. This approach showed in vivo cell proliferation activity with a hyaline-like cartilage production .
Our group has recently demonstrated that it is possible to isolate mesenchymal stromal cells from pathological IVD samples, and these cells exhibit stem-cell-like properties . Despite the fact that mesenchymal stromal cells represent a good in vitro tool to clarify the mechanisms underlying IVD degeneration, their use in cell therapy for spinal disorders remains unknown, mainly due to difficulty obtaining normal IVD tissue specimens as well as a sufficient number of cells required for therapy. Besides stromal cells derived from IVD tissue, it has been suggested that mesenchymal stromal cells derived from the adipose tissue (ADSCs) could be more accessible and effective cells to treat IVD disease ,. Indeed, ADSCs can be easily isolated from fat tissue of patients with IVD degeneration, and of relevance, they exhibit both proliferative and differentiation capability in appropriate culture conditions .
In the present study we assess the possibility to improve disc regeneration by intradiscal injection of ADSCs in the spontaneous and progressive model of IVD degeneration of Bgn−/0 mice, where IVD changes and degeneration occur due to byglican deficiency . We focused on the efficacy of the cell therapy monitoring treatment effects by high resolution in vivo imaging and ex vivo histological examination of IVD tissues. We additionally investigated whether ADSC implant increases the production of biglycan and aggrecan in the degenerated IVD.
ADSC isolation and expansion
The study was approved by the local institutional review board of the IRCCS Foundation Neurological Institute “C. Besta” (Milan, Italy), and conformed to the WMA Declaration of Helsinki. Patients’ informed consent to the procedure was obtained. Adipose tissue was collected from peri-umbilical adipose tissue from four healthy male donors (mean age, 45 ± 6 years) undergoing elective abdominal surgery. In particular, abdominal subcutaneous fat specimens of about 1 to 2 cm3 (corresponding to 1 to 2 g) were obtained by needle aspiration from the peri-umbilical area, under local anesthesia (1% xylocaine). Once the tissue was aspirated, the sample was placed in a Falcon tube containing Dulbecco’s phosphate-buffered saline (D-PBS) (Euroclone, Milan, Italy) (1:1, w/v) with the addition of penicillin and streptomycin solution (1%) (Sigma-Aldrich, Basel, Switzerland), and sent to the laboratory for tissue processing.
The adipose tissue was extensively washed with D-PBS and after centrifugation (300 g, 12 minutes), the infranatant, containing hematopoietic cells, was removed. The tissue was cut into small pieces with fine scissors (Martin KLS, Tuttlingen, Germany), and then mechanically dissociated using a 1-mL aerosol-resistant tip. Cells were resuspended in 10 mL D-PBS and centrifuged at 123 g for 10 minutes. The pellet was resuspended in 500 μL of D-PBS and again mechanically dissociated by a 200-μL aerosol-resistant tip. Cells were resuspended again and centrifuged as described above. Finally, the pellet was resuspended in 10 mL of chemically defined Stem Cells Medium (SCM) ,. The SCM composition consisted of DMEM-F-12 supplemented with 10% FBS (Gibco, Grand Island, NY, USA), 10 ng/mL basic fibroblast growth factor 2 (FGF2) (human recombinant, Peprotech, Rocky Hill, NJ, USA, or Upstate Biotechnology, Lake Placid, NY, USA), and 20 ng/mL epidermal growth factor (EGF) (human recombinant, Sigma-Aldrich, Milan, Italy). Cells were then seeded in tissue culture plates (NUNC, Thermo Scientific Illkirch, Cedex, France) at 1 to 3.5 × 103/cm2 density and were maintained in a humidified incubator with 5% CO2 at 37°C. After 24 to 48 h from plating, cultures were gently washed with D-PBS to remove unattached cells and then fed with fresh media. When cells achieved about 70% confluence, they were detached from the tissue culture plates using TrypLE Select (Gibco) and plated at a density of 5 × 103 cells/cm2. Cultures between passage 3 (P3) and passage 5 (P5) were expanded and used for experimental analyses. The remaining cells were cryopreserved in cryopreservation medium composed of dimethylsulfoxide (Sigma Aldrich) (10% in FBS).
Flow cytometric immunophenotyping
For each sample, 5 × 104 ADSCs between P3 and P5 were characterized by means of fluorescence-activated cell sorting (FACS). Cells were incubated with appropriate phycoerytrin (PE)- or fluorescein isothiocyanate (FITC)- conjugated monoclonal antibodies to test the expression of a pattern of mesenchymal, hematopoietic, endothelial and immunological markers including: CD14, CD34, CD45, CD73, HLA-DR (BD Pharmingen, San Jose, CA, USA), CD105 (AbDSerotec, Raleigh, NC, USA), CD90 (Millipore Temecula, CA, USA) and CD19 (Beckman Coulter, Cassina de’ Pecchi, Milano, Italy). After 30 minutes at 4°C, cells were washed once with D-PBS, fixed with 4% paraformaldehyde (PFA) (Sigma Aldrich), and analyzed using a FACS scan flow cytometer and Cell Quest software (BD Pharmingen, San Jose, CA, USA). According to the manufacturers’ instructions, specific isotype-matched mouse immunoglobulins (BD Pharmingen) were used as control. At least 2 × 104 events were acquired for each sample. Non-viable cells or cell debris were excluded by physical gating.
Multipotent differentiation capacity of ADSCs
ADSCs were tested for their capacity to differentiate into adipocytes, chondrocytes and osteocytes according to the minimal criteria suggested by Dominici et al.. The procedure was described by Navone et al.  (Materials and methods).
Procedures involving animals and their care were conducted in conformity with all procedures following institutional guidelines which, in turn, are in compliance with national (DL number 116, GU Suppl. 40, February 18 1992, Circolare number 8, GU, 14 July 1994) and international laws and policies (EEC Council Directive 86/609, OJ L 358, 1 December 2012, 1987; NIH Guide for the Care and Use of Laboratory Animals, US National Research Council, 1996). The protocol for the use of laboratory animals was approved by the ethical committee of the IRCCS Foundation Neurological Institute “C. Besta” (Milan, Italy), and by the Italian Ministry of Health (number NTN-01-10). Bgn−/0 mice, generated by gene targeting in embryonic stem cells , were kindly provided by Dr Marian Young (National Institutes of Health, Bethesda, MD, USA), Dr Ariane Melchior-Becker and Dr Jens W Fischer (University of Essen, Germany) and Dr Liliana Schaefer (Johann Wolfgang Goethe-University, Frankfurt, Germany). C57Bl6 mice were purchased from Charles River (Calco, Lecco, Italy). We used male mice for experimental animals because the biglycan gene is located on the X chromosome and absent from the Y chromosome. All mice maintained their hybrid (C57Bl6/129) genetic background. DNA was isolated from tail samples, and the genotype of the wild type (WT) and Bgn−/0 mice was determined by PCR . The successful genetic deletion in Bgn−/0 mice was previously assessed by the absence of biglycan mRNA and protein . Animals were enrolled at 6 months of age and characterized for disc degeneration until 19 months by 7TMRI (7 T Biospec 70/30 USR, Bruker, Ettlingen, Germany). C57Bl6 (n =10) male mice were considered as WT controls. All animals were supplied with food and water ad libidum. Temperature, humidity and night-day cycles were maintained according to the standards set up by the research animal services.
MRI characterization of the animal model
In order to study the timing of disc degeneration and evaluate the time of cell implantation, Bgn−/0 mice (n =10) and WT mice (n =10) were monitored every 2 weeks from 6 months to 18 months of age with the same acquisition protocol.
Preparation of ADSCs for transplant
ADSCs isolated from the four donors satisfied criteria proposed by Dominici et al. . Briefly, ADSCs, which are plastic-adherent when maintained in standard culture conditions, expressed CD105, CD73 and CD90, and lacked expression of CD45, CD34, CD14, CD19 and HLA-DR surface molecules. When cultured in a selective culture condition, ADSCs were able to differentiate into osteoblasts, adipocytes and chondroblasts. After four in vitro passages, ADSCs derived from one donor were harvested by Tryple Select (Gibco), washed and resuspended in saline solution.
Procedure of ADSC injection into the IVD in Bgn−/0 mice
At 16 months of age, after confirmation of disc degeneration by 7TMRI, ADSCs or saline were administrated according to the following procedure. General anesthesia, consisting of induction with 5% isoflurane (Aerrane, One Baxter Parkway, Deerfield IL, USA) in 30% oxygen in air at a flow rate of 1 L/minute was given, and anesthesia was maintained with 2.0 ± 0.4% isoflurane. Five minutes after induction of anesthesia, supplemental analgesia was provided by intraperitoneal injection of buprenorphine (Sigma Aldrich) (0.3 mg/kg in saline, 1 mL given over 5 minutes). With the animals (n =10 each for placebo and the ADSC-transplanted group) lying supine, both the abdominal skin and peritoneum were incised. The bowel was displaced to allow an anterior approach to the lumbar vertebral segment. IVD at the level of the first lumbar vertebra (L1) to L2 was exposed and ADSCs or saline treatment was administrated by a Hamilton syringe (using a 33-gauge blunt needle). Cells (8 × 104) or saline were injected 1 mm deep in a final volume of 5 μL in a time of 2 minutes. After injection, the needle was maintained inside the disc for a further 2 minutes to reduce the spilling of the injection solution. The bowel was then repositioned and the wound was closed using 5–0 Nylon suture (Ethicon Inc., Somerville, NJ, USA). Post-intervention animals were left to recover on heated pads and then transferred to their own cages, and monitored daily for 3 months.
The effectiveness of ADSC transplantation on L1 to L2 discs was evaluated by 7TMRI of the lumbar tract of the spine one day before transplantation, immediately after surgery (30 minutes) and every 14 days until 12 weeks after transplantation. The acquisition protocol was optimized in order to reduce exposure time to anesthesia.
The experiments were carried out using a high-field 7TMRI (Bruker) scanner equipped with a gradient system reaching the maximum amplitude of 400 mT/m. Mice were anesthetized with 1.5 to 2.0% isoflurane (flow rate 0.8 L/minute) and positioned on an animal bed equipped with a nosecone for gas anesthesia. To detect the depth of anesthesia and the animal health condition during the MRI study, the respiratory rate and temperature were monitored by a pneumatic and rectal sensor, respectively. A 75-mm birdcage linear coil (Rapid Mr International, Columbus, OH, USA) was used for radio frequency excitation and a rat brain surface coil (Rapid) was used for signal reception. Animals were placed supine on the rat brain surface coil, so that the lumbar tract of the spine could be placed at the centre of the coil’s sensitive part. For anatomical references and to test the correct animal alignment in the magnet bore, T2-weighted images (T2-wi) were acquired in three orthogonal planes: axial, sagittal, and coronal. The acquisition protocol included T1- and high-resolution T2-wi. T1-wi was acquired by spin echo sequence with echo time (TE) 11.720 ms, repetition time (TR) 401.306 ms, slice thickness (ST) 1 mm, in-plane resolution 0.105 mm, number of averages (NA) 6 and high resolution T2-wi by a rapid acquisition with relaxation enhancement (RARE) sequence (TR/TE =3000/14 ms, RARE factor =8, slice thickness =0.07 mm, in plane resolution =0.086 mm, NA =8). Both sequences investigated the three orthogonal orientations: axial, coronal and sagittal.
MRI assessment of IVD regeneration after ADSC transplantation
Once the acquisition protocol had been optimized and implantation time determined, the whole protocol was repeated on mice in the placebo group (n =10) and in the ADSCs group (n =10), every two weeks for three months after implantation; the mouse being placed in the same position for easier inter-scan comparison.
A signal intensity index was determined to assess the degree of disc regeneration after transplantation. The operated discs were identified on the high resolution T2-wi and the signal intensity was quantified on the corresponding axial T1- and T2-wi slice using Paravision software (Paravision 5.1, Bruker). A circular region of interest of 1 mm2 was drawn at the center of the disc and in the adjacent spinal cord at every time point. The signal intensity from the spinal cord was used as the intensity reference within the scan and the index was therefore defined by the ratio between the disc and the spinal cord signals; thus the normalized indexes could be compared between different animals at different times . Mean values were computed in the L1 to L2 disc where histological examination detected the presence of implanted cells. The selection of regions of interest was repeated independently by two blinded reviewers and the mean from the two values was considered.
Animals were sacrificed at 12 weeks after ADSC injection. The L1 to L4 vertebral bodies were entirely fixed in 4% PFA containing 0.1 M sodium phosphate buffer (Euroclone). After 3 weeks of decalcification with RapidCal Immuno (BBC Biochemical, Mount Vernon, WA, USA), the tissues were embedded in Optimal Cutting Temperature (OCT) compound (Sakura Finetek, Torrance, CA, USA) and sectioned to 20 μm thickness. The sections were stained with Safranin-O (Sigma Aldrich) and counterstained with human specific anti-HuNu antibody (MAB 1281, Chemicon Millipore, Billerica, MA, USA) (1:100) to identify human cells. The histological grading system for disc degeneration devised by Masuda  was used, focusing on the morphological changes in the IVD structure. Each sample was interpreted by two blinded histologists. The histological evidence of disc regeneration was interpreted considering the recovery of tissue matrix and IVD structure .
The disc sections were incubated overnight at 4°C with the appropriate primary antibody against Human Nuclei (HuNu), biglycan, aggrecan, Ki67 and Iba1, diluted in 1% bovine serum albumin (BSA) in D-PBS. Sections were then washed in D-PBS containing 0.1% BSA and incubated 1 h at room temperature (RT) with a secondary antibody conjugated with a fluorochrome (Molecular Probes). Sections were then washed and mounted in Vectashield H-1000 (Vector Laboratories, Peterborough, UK). The following primary antibodies were used: mouse anti-HuNu (1:100 dilution; Chemicon,), goat anti-human biglycan (1:250; Abcam, Cambridge, UK), goat anti-human aggrecan (10 μg/mL; R&D Systems, Minneapolis, MN, USA), rabbit anti-human Ki67 (1:200; Chemicon), rabbit anti-mouse Iba1 (1 μg/mL; Wako Chemicals GmbH, Neuss, Germany). Nuclear staining (1:5000; 4',6-diamidino-2-phenylindole (DAPI), (Invitrogen, Life Technology, Monza, Italy) was applied and used to quantify the total number of cells. Immunohistochemistry acquisitions were performed by two blinded observers.
Images of cells positive to HuNu (as a marker of injected ADSCs), and to biglycan and aggrecan (as markers of in vivo differentiation) were acquired by microscopy (Leica TCS SP2 AOBS, Leica Microsystems, Milan, Italy) after specific immunocytochemical staining at 3 months after transplantation. The quantification of positive cells was performed by Axion Vision Software (Carl Zeiss Microscopy GmbH, München Germany). Briefly, cell counts were performed on a minimum of nine independent fields of photomicrographs captured with 40X objective. Total counts of each marker’s immunoreactive cells were performed, and the number of positive cells per culture was expressed as percentage of total cells and of HuNu-positive cells.
The intensity index variation over time was evaluated by SPSS software (IBM). Repeated-measures analysis of variance (ANOVA) was performed pairwise at 3, 5 and 12 weeks post surgery with respect to baseline and between the groups at the same week. P-values lower than 0.05 were considered statistically significant. For each cell-treated animal, we estimated the correlation between intensity index and number of ADSCs found in the disc at the histological exam.
ADSC culture and phenotypic characterization
ADSCs were isolated from human adipose tissue sample obtained from healthy donors. After seeding in the used culture conditions, isolated ADSCs grew as adherent monolayer and presented a fusiform, fibroblastic-like morphology.
Identification of degeneration and regeneration from 7TMRI findings
Twelve weeks after treatment, the slices of ADSC-implanted discs were immunopositive for both Safranin-O and anti-HuNu, which identify the ECM and human cells, respectively (Figure 4B).
The human cell number observed in the middle of the section of the cell-transplanted disc exhibited an appreciable correlation with the intensity index obtained by MRI examination of the corresponding mouse (Figure 4C). The correlation analysis was conducted in a group of eight implanted discs and the mean value of the placebo group was shown. The linear regression coefficient was R =0.73, with a positive slope.
Histological analyses of IVD treated with ADSCs
ADSCs, placebo and WT groups were also investigated for the immunoinflammatory marker ion calcium binding protein (Iba1), which is specifically expressed in macrophages and activated microglia. In placebo sections, we observed an average of 45 to 50 positive cells per field (Figure 5G). Conversely, reactive cells in the ADSC group were by far less numerous (5 to 6 per field), and were characterized by a low intensity staining (Figure 5H). The number of positive cells in the ADSC group was found similar to that of WT samples (Figure 5I).
Expression of HuNu, biglycan, aggrecan and Ki67 in mice treated with ADSCs and placebo
In order to assess whether the ADSCs expressed aggrecan spontaneously, we performed immunohistochemistry on control cells and on cells growing in standard culture conditions, that is, in the absence of chondrogenic inducing factors. In both cases, we found that immunopositivity to aggrecan was undetectable in cultured ADSCs under normal expansion conditions (data not shown), indicating that they did not spontaneously express this large proteoglycan prior to implantation.
Finally, due to the significant presence of human ADSCs in transplanted mice, in order to ascertain whether ADSCs may undergo proliferation, we analyzed the expression of Ki67 at 12 weeks from ADSC injection. However, in Bgn−/0 mice at 12 weeks after implant, co-localization of HuNu and Ki67 staining was undetectable (Figure 8C,D).
Different mouse models have been proposed to study the physiological and pathophysiological behavior of degenerated IVD in spinal disorders. Numerous methods have been developed, including mechanical instability, mechanical compression, structural and chemical injury ,. However, these models do not appear to entirely reflect disc degeneration, but rather they mirror post-surgery disc injury ,.
The Bgn−/0 mouse model exhibits many similarities to the human IVD pathophysiology, and despite not entirely reproducing it, it was reported to represent a valuable model for studying the time progression of IVD degeneration as a chronic and linear degenerative process in vivo. Thus we considered the Bgn−/0 mouse as a suitable tool for our preliminary in vivo evaluation of the potential efficacy of ADSC implants as a therapeutic approach in progressive, degenerative disc disease.
In a previous study on Bgn−/0 mice, the degree of degeneration or deceleration of the disc degeneration process was evaluated by histological/immunochemical approach . This type of evaluation of the IVD degeneration allows the identification of alterations in cell proliferation and ECM synthesis, but cannot provide information on the progression or arrest of the disease over time. Instead, changes in MRI signal intensity on T2-wi of IVDs, represents an important parameter for evaluating the degree of disc degeneration . Indeed, a decrease in signal intensity of T2-weighted MRI images correlates with the IVD water content, which in turn is associated with reduction in nuclear proteoglycans, a main feature of disc degeneration . Thus, in the case of disc regeneration, the high-signal intensity in the T2-wi is restored, reflecting restoration of proteoglycan and water content . It is for these reasons that in the present investigation we first followed the time progression of IVD degeneration in Bgn−/0 mice by high resolution MRI, and then processed discs for histological analyses.
Our studies, performed by 7TMRI assessment and histological evaluation, confirmed that IVD of Bgn−/0 mice were in a more advanced degenerative state than those of WT mice at every age examined, and thus, the biglycan deficiency significantly accelerated disc degeneration. By 7TMRI assessment, we found that IVD degeneration was particularly severe in Bgn−/0 mice at 16 months of age. For this reason we started the cell therapy at this time.
Diverse therapeutic approaches have been proposed to halt or reverse IVD degeneration . These include treatments with anabolic growth factors  and, more recently, cell therapy using either intradiscal administration of NP-derived cells, or MSCs of different tissue origin ,,. In this context, the use of ADSCs was recently proposed as a potential and effective therapeutic tool for the treatment of IVD degeneration . Prompted by this evidence, we used human ADSCs isolated without enzymatic digestion from abdominal adipose tissue specimens. These cells in culture exhibit proliferative activity, maintain typical mesenchymal markers, as well as differentiation potential .
Some evidence of IVD regeneration in an autologous ADSC-injected rabbit model has been previously provided . The present study shows for the first time that ADSC transplantation is beneficial in ameliorating degeneration in a chronic model of IVD, as demonstrated by MRI, histological and immunofluorescence findings.
In particular, the ameliorative effect of ADSCs on IVD degeneration was evident as MRI index values at all investigated times, with significant differences when compared to the pre-operative value. Of relevance, the MRI index values of the ADSC-treated group were significantly higher than those of the placebo group at all investigated times. Moreover, we found that the MRI intensity index correlated with the number of cells found in the implanted discs, supportive of an increment in water content and proteoglycans synthesis in the presence of ADSCs. The histological assessment by Safranin-O staining confirmed that ADSC implants improved the structure of IVD in Bgn−/0 mice. Indeed, we observed a recovery of disc structure, supporting that neosynthesis of ECM components occurred in transplanted discs. However, it is important to note that transplanted cells may also have transient paracrine effects, and their survival in the site of injection could not be the only one relevant aspect involved in disc regeneration .
Although the beneficial effects of ADSC transplantation were already significant after 3 weeks, these effects appeared not to progress, but rather to be maintained along with time. Notwithstanding the ameliorative effects of ADSC transplantation on disc degeneration, the apparent lack of increased beneficial effects over longer periods of time may indicate that a unique treatment could not be sufficient for optimal therapy, and that different treatments (in terms of schedules and/or transplanted cell number) could be more effective than the one used for longer periods. Further experiments are needed to clarify if serial transplants, and/or a higher number of implanted cells, as well as ADSC injections at earlier degeneration times could be effective in ameliorating the recovery process of IVD degeneration.
Immunofluorescence analyses performed with antibodies against human HuNu, Ki67, biglycan, and aggrecan provided additional important results, which we subsequently discuss here. Of critical importance, our data revealed the presence of HuNu positive cells, that is, of human cells, in transplanted IVDs all over time, and up to 12 weeks post-transplant. Thus, it emerges that, after implantation into the degenerated IVDs of biglycan-deficient mice, some human ADSCs can survive for at least 12 weeks in the peculiar microenvironment of the IVD, where hypoxia, low nutrition, acidic pH, mechanical loading, endogenous proteinases, and cytokines  would not favor exogenous ADSC survival. We also observed some positivity for anti-HuNu also in the adjacent discs, possibly due to the leakage of cells during injection.
However, notwithstanding the presence of ADSCs in IVDs, at 12 weeks we were unable to find any evidence of cell division, as the proliferation marker Ki67 was undetectable at this time. However, taking into account that 12 weeks is a prolonged time after transplantation, we cannot exclude that ADSC proliferation may occur at earlier times. As indirect support of this hypothesis, histological images revealed that the implanted cells are present as tight clusters of cells, which often indicates a sign of cell division. Thus, ADSCs might have undergone cell division in the early weeks and then stopped in the later weeks.
Additional important evidence provided by our study is that a relevant percentage of ADSCs transplanted on IVD of Bgn−/0 mice showed positivity to anti-human biglycan, and also to aggrecan, supporting the concept that a differentiation process in ADSCs has occurred at 12 weeks from transplant. This is in agreement with previous studies on cultured cells, demonstrating the stem cell population within the adipose stromal compartment in human processed lipoaspirate can differentiate toward the osteogenic, adipogenic, myogenic, and chondrogenic lineages, and that they express biglycan and aggrecan in chondrogenic differentiation conditions . Notably, although human mesenchymal stem cells have been reported to spontaneously express some ECM proteins such as cartilage oligomeric matrix protein , we obtained evidence that ADSCs did not spontaneously express aggrecan when cultured in the absence of chondrogenic inducing factors, that is, in the normal expansion conditions we used prior to implantation. Therefore, it emerges that human ADSCs are multipotential stem cells capable of undergoing chondrogenic differentiation in vivo, and it is suggested that the diseased disc environment is able to induce the expression of both biglycan and the cartilage specific proteoglycan aggrecan. Whereas both proteins appear to be de novo produced by implanted ADSCs, as placebo-treated mice showed some positivity to anti-human aggrecan antibody, we cannot exclude that ADSCs treatment may stimulate an endogenous production of aggrecan too, by a paracrine effect of the cells in the disc.
Overall, it is tempting to speculate that, once implanted into IVDs, ADSCs initially may undergo cell division and forms tight clusters, and subsequently, stimulated by the local microenvironment, close-fitting clusters of ADSCs undergo chondrogenic differentiation. In agreement, cell density was reported to be crucial for chondrogenic differentiation, pellet mass cultures being essential for the chondrogenic differentiation of MSCs .
Two further important findings of our study deserve comments. First, it is worth noting that the ameliorative effect of ADSC implant on disc degeneration was observed in old animals and these had severe disc damage. This underlies the potential of ADSC implant as effective in our in vivo mouse model. Second, during the study period, we did not observe any host-graft rejection, further supporting the effectiveness of ADSC implants in IVDs. In this context, the survival of IVD-implanted ADSCs may be favored by the fact that the IVD represents a privileged implantation site from the immunological point of view, mesenchymal stem cells derived from different adult tissues showing advantages from these immunosuppressive effects -.
In conclusion, our study shows for the first time that the ADSC treatment can be beneficial in vivo in a mouse model of spontaneous IVD degeneration. ADSCs exert their effects at various levels, overall positively influencing the degeneration process and finally exhibiting long-term engraftment and tissue recovery. ADSCs appear effective in IVD degeneration by providing exogenous biglycan, and simultaneously stimulating the endogenous production of aggrecan, both these proteoglycans being crucial in re-establishing the IVD matrix composition closer to the normal one .
Overall, results obtained in this study provide preliminary in vivo evidence that ADSC transplants may represent an effective treatment for degenerative disc disease in humans. Although the Bgn−/0 mouse is a valuable model for investigating disc degeneration , it is worth noting that this model does not entirely reproduce the human disc pathophysiology. Future investigations in different models such as non-human primate models are prompted by this research, and will hopefully confirm the validity of the proposed therapy.
Marfia Giovanni and Campanella Rolando are co-first authors.
We would like to thank Dr Marian Young, Dr Ariane Melchior-Becker, Dr. Jens W Fischer, and Dr Liliana Schaefer for the Bgn−/0 mouse model.
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