- Open Access
Nascent osteoblast matrix inhibits osteogenesis of human mesenchymal stem cells in vitro
© Kolf et al. 2015
- Received: 29 December 2014
- Accepted: 3 November 2015
- Published: 22 December 2015
Adult mesenchymal stem cells (MSCs) are considered promising candidates for cell-based therapies. Their potential utility derives primarily from their immunomodulatory activity, multi-lineage differentiation potential, and likely progenitor cell function in wound healing and repair of connective tissues. However, in vitro, MSCs often senesce and spontaneously differentiate into osteoblasts after prolonged expansion, likely because of lack of regulatory microenvironmental signals. In vivo, osteoblasts that line the endosteal bone marrow surface are in close proximity to MSCs in the marrow stroma and thus may help to regulate MSC fate.
We examined here how osteogenic differentiation of MSCs in vitro is affected by exposure to osteoblastic cells (OBCs). Human bone marrow MSCs were exposed to OBCs, derived by induced osteogenic differentiation of MSCs, either directly in contact co-cultures, or indirectly to OBC-conditioned medium or decellularized OBC extracellular matrix (ECM).
Our results showed that OBCs can act as negative regulators of MSC osteogenesis. mRNA expression profiling revealed that OBCs did not affect MSC osteogenesis in direct contact cultures or via secreted factors. However, seeding MSCs on decellularized OBC ECM significantly decreased expression of several osteogenic genes and maintained their fibroblastic morphologies. Proteomic analysis identified some of the candidate protein regulators of MSC osteogenesis.
These findings provide the basis for future studies to elucidate the signaling mechanisms responsible for osteoblast matrix-mediated regulation of MSC osteogenesis and to better manipulate MSC fate in vitro to minimize their spontaneous differentiation.
- Mesenchymal stem cells
- Extracellular matrix
- Stem cell niche
Mesenchymal stem cells (MSCs) are multipotent cells resident in adult tissues that function in wound healing and repair of connective tissues, especially the musculoskeletal system. Capable of extensive expansion in vitro , they are an exciting cell type to study because of their therapeutic potential in tissue engineering and regenerative medicine . MSCs are commonly differentiated into osteoblasts, chondrocytes and adipocytes , as well as other cell types [4, 5]. Still more promising, MSCs have been shown to have immunomodulatory properties, allowing them to evade the immune system when transplanted .
A practical hurdle in the application of MSCs is their tendency to undergo spontaneous differentiation upon extended propagation in vitro. Specifically, osteogenesis appears to be the default differentiation pathway for long term cultures of MSCs , causing them to senesce and lose their therapeutic potential. However, in vivo, both of these processes are prevented due to the specialized niche in which MSCs reside. Recapitulation of this niche in vitro would permit more extensive expansion of MSCs without the loss of their multi-lineage differentiation potential. The feasibility of such an endeavor requires understanding the nature of the MSC niche.
In the bone marrow, the MSC niche is, at least partially, perivascular . However, MSCs are likely in contact with both endothelial cells and osteoblasts (OBs), which line the bone marrow cavity. Since OBs have been implicated in the hematopoietic stem cell niche [9, 10], it seems likely that they could also be key players in the MSC niche. A number of studies have assessed the effects of OBs and their secreted soluble and extracellular matrix (ECM) proteins on MSC osteogenesis [11–15]. For example, co-culturing of embryonic mouse MSCs and OBs, separated in a Transwell set-up, showed that factors secreted by OBs can cause a 30-fold increase in MSC proliferation and a decrease in their alkaline phosphatase (ALP) activity, indicative of less osteogenic differentiation . While the active factors responsible for this observed effect have not been ascertained, both bone morphogenetic proteins (BMPs) and insulin-like growth factors (IGFs) are secreted by OBs and have been implicated in several niche functions in other systems, including stem cell maintenance [16-18] and asymmetric cell division .
On the other hand, both BMPs and IGFs can also be found sequestered in the ECM of OBs; in fact, BMPs were first identified in demineralized bone matrix (DBM) because of their activity in inducing bone formation . While several ECM molecules, in their purified forms, have been shown to enhance bone formation (e.g., collagen type I ), the reactivity of MSCs to native OB matrix, with its three-dimensionality and protein-protein interactions, is likely to be more complex. In addition, it is important to examine the interactions between human MSCs and nascent human OBs, the most likely osteoblastic cell type to interact with MSCs in the native bone marrow environment. Mature bone cells, such as fully differentiated OBs and osteocytes, from which DBM is created, are encased in bony matrix and are most likely exposed to MSCs only upon tissue injury, such as bone fracture. This information serves as the foundation for our study of MSC osteogenesis, in which we tested the effects of relatively immature osteoblastic cells (OBCs), derived in vitro from MSCs. Specifically, we have examined the influence of cell-cell interaction, and secreted factors and extracellular matrix produced by the OBCs on MSC osteogenic differentiation.
Human femoral heads were generously obtained from Dr. Paul Manner (University of Washington, Seattle) from total hip arthroplasty patients with informed consent and Institutional Review Board approval. Bone marrow MSCs were isolated as described previously , plated in expansion medium (EM) (DMEM, 9 % lot-selected fetal bovine serum (Invitrogen, Grand Island, NY; MSC-qualified), 1 % penicillin/streptomycin/Fungizone) in 150-cm2 culture flasks (Corning or Nunc), and incubated at 37 °C, 5 % CO2. One to two days later, hematopoietic cells were rinsed away with phosphate-buffered saline (PBS) or Hank’s Balanced Salt Solution (HBSS). MSCs were routinely passaged every three to four days before reaching confluency.
To obtain OBCs, second or third passage MSCs were trypsinized and re-plated in osteogenic medium (OM) consisting of EM plus 10 mM β-glycerophosphate, 19.5 mM L-ascorbic acid-2-phosphate, 10 nM dexamethasone (all from Sigma-Aldrich, St. Louis, MO, USA), 10 nM 1,25-dihydroxyvitamin D3 (Enzo, Farmingdale, NY, USA) . MSCs were cultured in OM for a minimum of 14 days before being considered OBCs.
Direct co-cultures of MSCs and OBCs
To assess endogenous levels of osteoblastic mRNAs in osteogenically differentiating MSCs in contact with OBCs, MSCs and OBCs were co-cultured in a 1:4 ratio at 9,000-10,000 cells/cm2. Before co-culture, trypsinized MSCs were stained with the cell tracker CM-DiI (Thermo Fisher, Waltham, MA; 106 cells/mL + 8 μL CM-DiI, 37 °C, for five min, then 4 °C, for 15 min) to distinguish them from OBCs and to allow subsequent fluorescence-activated cell sorting (FACS). Three co-culture combinations were tested in both EM and OM: (1) DiI-labeled MSCs mixed with unlabeled OBCs, (2) DiI-labeled MSCs mixed with unlabeled MSCs, and (3) unlabeled, MSC-only cell populations, with the latter two conditions serving as controls. Samples were harvested pre-culture, and at culture days 6 and 12. MSC-only cultures were trypsinized, centrifuged, resuspended in 1 mL Trizol (Invitrogen), and stored at -80 °C; mixed cultures were trypsinized and frozen in dimethyl sulfoxide (DMSO) freeze medium (BioVeris Corporation, Gaithersburg, MD, USA) until the time course was complete. The DiI-positive cells were fractionated using a Becton-Dickinson three-laser Dako MoFlo FACS sorter, pelleted by centrifugation, resuspended in 1 mL Trizol, and stored at -80 °C. Osteogenesis was assessed by conventional real time RT-PCR and by PCR array analysis (SuperArray, Qiagen, Valencia, CA, USA; see below).
Conditioned medium cultures
To assess the effects of OB-secreted factors on MSC osteogenesis, EM and OM were conditioned for three days by OBCs that had completed 11-14 days of osteogenesis. Conditioned medium (CM) was frozen at -80 °C until use. OM incubated without cells for three days, referred to as aged osteogenic medium (AOM), served as the control. Thawed CM was mixed 1:1 with fresh OM before use (Note: Fresh OM was added to minimize possible medium nutrient deprivation as a confounding factor). MSCs, seeded at 8-10 × 103 /cm2 in 6- and 12-well plates and exposed to CM every three days, were analyzed for osteogenesis, as described below.
The effects of devitalized/decellularized OBC ECM on MSC osteogenesis were analyzed as follows: MSCs seeded at a density of 8-10 × 103 cells/cm2 in 6-well plates were cultured in OM for at least 14 days, rinsed with HBSS, and decellularized by lysis, either with three washes of 3 mL/well MilliQ-purified water (ddH2O) or by one wash of 1 mL/well 0.5 % deoxycholate (Sigma-Aldrich) in ddH2O (DOC) for 30 min at 4 °C. The plates were then washed with HBSS three times for at least three min each time. Live/Dead staining (Invitrogen) was performed in one well of each treatment type to ensure 100 % cell death. MSCs were then seeded at 8-10 × 103 cells/cm2 on top of the two types of matrix, with tissue culture plastic as the control, and osteogenesis was assessed as described below.
MSC proliferation was assessed fluorimetrically (494 nm/567 nm), based on calcein incorporation and Ca2+-dependent fluorescence, after Live/Dead staining (Invitrogen) performed on a Wallac Victor2 V plate reader (Perkin Elmer, Waltham, MA, USA). Nine measurements were made in a 3 × 3 pattern within each well of a 24-well plate, corrected with readings of matrix without cells.
RNA extracted from frozen Trizol samples was reverse transcribed using oligo-d(T) and a First Strand Synthesis kit (SSII, Invitrogen) and the cDNA was amplified using SybrGreen (BioRad, Hercules, CA, USA) on an iCycler (BioRad). Primer sets (5′–3′) were designed (see Additional file 1: Table S1) for the following human genes: osteocalcin (OC), ALP, Runx2, collagen type I, α2 (Col I), and glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Standard curves generated using a 10-fold dilution series created from a single batch of cDNA from day 18 OBCs derived from a single donor allowed relative comparisons of mRNA copy numbers between donors and experiments. Expression levels were normalized to GAPDH in triplicate.
Human osteogenesis RT2 Profiler™ PCR Superarrays (SABiosciences; http://www.sabiosciences.com/PCRArrayPlate.php) were used to monitor 84 different genes associated with osteogenesis. For the matrix study, 500 ng of cDNA were loaded per plate (5 ng/well). Since FACS sorting yielded limited cell numbers in the co-culture experiments, these samples were pre-amplified by 12 rounds of PCR prior to loading them on the Superarray plates. A total of 17.5 ng of mRNA was pre-amplified using RT2 Nano PreAMP cDNA synthesis kits plus the corresponding NanoAmp osteogenic primers (SABiosciences) according to the manufacturer’s protocol.
The fluorescence threshold for each plate was adjusted to give an average positive PCR control (PPC) value of 20 ± 2 cycle thresholds (CTs). Transcripts whose CTs were >35 were assumed to be absent . For pre-amplified samples, the cut-off CT was 30, as recommended by the manufacturer (personal communication, SABiosciences representative).
Data analysis was carried out via the SABiosciences web portal. The geometric mean of the housekeeping gene CT values was subtracted from the CT value of each gene of interest for normalization. Housekeeping genes whose CT values varied by more than two-fold among the conditions were excluded.
Osteogenic differentiation assays
To visualize matrix mineralization, cultures were stained with 2 % Alizarin Red S (AlzR), pH 4.2 (Rowley Biochemical Institute, Danvers, MA, USA). ALP activity was monitored histochemically using the Fast Blue, leukocyte alkaline phosphatase kit (Sigma, 86R-1KT).
Histochemical staining was imaged at low (5X) and high (63X) magnifications, and as whole-plate scans at a resolution of 2,400 ppi. Fluorescent Live/Dead staining was examined at 10× magnification and images analyzed using AxioVision software.
2D-Differential in-gel electrophoresis (2D-DIGE) and protein identification
OBCs were cultured from three different MSC donors and lysed as described for the matrix cultures. After the final rinse, matrix proteins were extracted using 7 M urea, 2 M thiourea, 30 mM Tris-HCl, 4 % CHAPS, pH 8.8 and stored at -80 °C until use. Proteins were precipitated using the 2D Clean Up Kit (GE Healthcare Bio-Sciences, Pittsburgh, PA, USA) and quantified by the 2D Quant Kit (GE), with pH adjusted to 8.0 - 9.0. A standard was created by mixing together equivalent aliquots of each sample.
Solutions of CyDyes 2, 3, and 5 (GE) in dimethylformamide (Sigma) were added to the samples at final concentrations of 400 pmol per 50 μg protein. The standard was labeled with Cy2 while individual samples were labeled with either Cy3 or Cy5, assigned randomly, for 30 min on ice in the dark, followed by quenching with lysine (Sigma). Samples were flash frozen and stored at -80 °C until use.
First dimension gel rehydration and sample loading
Thawed samples were equilibrated (1:1, v/v) with 2× sample buffer (7 M urea, 2 M thiourea, 4 % CHAPS, 4 % IPG 3-10, 6.2 mg diothiothreitol/mL) and pooled appropriately. Each mixture was added to rehydration buffer (7 M urea, 2 M thiourea, 4 % CHAPS, 2 % IPG 3-10, plus 12 μL DeStreak Solution [GE]/mL before use) for a total volume of 340 μL, and used to rehydrate an Immobiline™ 18 cm IEF DryStrip, pH 3-10 (GE) overnight.
A Multiphor II electrophoresis unit (GE Healthcare Bio-Sciences) was used with the following program at 20 °C in the dark: constant current of 1 mA; constant power of 5 W; 500 V for 0.01 h; 500 V for 3 h; gradual ramping from 500 to 3,500 V over 5 h; and 3,500 V for 12.5 h. Unless used immediately for second dimension electrophoresis, IEF gels were wrapped in plastic, placed in airtight tubes, flash frozen in liquid nitrogen, and stored at -80 °C until use.
SDS-polyacrylamide gel electrophoresis
The second dimension gels were 1 mm thick, 4-20 % SDS-polyacrylamide gels cast in low-fluorescence glass plates (Jule Biotechnologies, Milford, CT, USA). Electrofocused gels were incubated for 15 min in the dark in reducing buffer (0.5 M Tris-HCl, pH 6.8, 10 mg dithiothreitol/mL), followed by incubation for 15 min in alkylation buffer (10 % reduction buffer without dithiothreitol, 6 M urea, 30 % glycerol, 1 % SDS, 25 mg iodoacetamide/mL), placed on the SDS gel, and sealed with 1 % low-melt agarose. Fluorescent Mr standards (Sigma) were used. Electrophoresis was run at 25 °C (2 W/gel, 45 min; 17 W/gel, 3-4 h). Gels were stored moist in the dark at 4 °C overnight.
CyDye-protein fluorescence was imaged on a Molecular Dynamics Typhoon 9410 Variable Mode Imager at a resolution of 100 pixels/μm. The gel that would be used for picking protein spots (“pick gel”) was then stained with SimplySafe Coomassie blue (Invitrogen), and fixed using two to three cycles of a 15 min wash in 10 % ethanol, followed by a 15 min wash in water. The Coomassie staining of the pick gel was then imaged.
Protein spot comparison: DeCyder™ analysis
Gel images were analyzed using DeCyder™ (GE) to detect protein spots in each gel. Spots were excluded if they had slopes >1.3, areas <260 pixels, volumes <45,000 pixels, and peak heights <600 or >65,000 relative fluorescence units. Spots resulting from the Mr standards were also excluded to prevent them from being used in the statistical analysis of biological variance. The rest of the spots were analyzed manually to ensure accurate discrimination. The software then used the Cy2 standard, included in each gel, to match each protein spot to its related spots in the other gels. This matching was again checked manually and corrected, as needed. Finally, a “pick list” was generated by comparing all occurrences of each spot between gels and choosing those spots whose average volumes were > ±1.5-fold different from the standard (p ≤ 0.05).
Mass spectrometric identification of protein spots
Protein spots from the “pick list” were cut out of the gel in 1 mm2 pieces, destained, and digested overnight at 37 °C in trypsin (0.02 μg/μL in 25 mM Tris-HCl, pH 8.0) (Promega, Madison, WI, USA) to just cover the gel pieces, with extra buffer on top. Peptides were extracted with 60 % acetonitrile/3 % trifluoroacetic acid and dried.
Mass spectrometry analysis of gel digest samples was generously performed by Dr. Lewis Pannell (University of Alabama). Samples, dissolved in 15 μL 1 % acetic acid/2 % acetonitrile, were run on an ESI-TRAP mass spectrometer (ThermoElectron LTQ Orbitrap) coupled to an Agilent 1200 nano LC system with a C18 reverse phase column, eluted with 5-90 % acetonitrile (in 0.2 % formic acid) over 40 min. The acquired data files were converted into Mascot generic format (.mgf) and matched against the Swiss Protein (Sprot) Homo sapiens database through the MASCOT search engine (http://www.matrixscience.com). The following additional parameters were used: fixed iodoacetamidation of cysteines, variable deamidation, standard scoring, and requiring at least one unique peptide per protein match (“require bold red”). Mass accuracy for precursor ions was set to ±10 ppm and ±0.6 Da for MS/MS fragmentation data. Only proteins with at least three significant peptide matches (p < 0.05) and ion scores ≥200 were considered. Proteins that were identified in gel blanks or that matched the proteins of the Mr markers were excluded from further analysis.
In silico analysis and compilation of gene expression profiles and 2D-DIGE protein data was performed using Ingenuity Systems software (Qiagen). Changes ≥3-fold of normalized gene expression from MSCs in OM on matrix versus plastic were analyzed with their corresponding p-values (≤0.1). For each gene, the fold change at day 6 or day 12 that had the higher value and/or the greater significance was chosen to represent that gene. Proteins identified by mass spectrometry in the 2D gels were analyzed together with their maximum scores from Mascot.
All statistical comparisons used an unpaired Student’s t-test with a p-value of ≤0.05, unless otherwise specified. Graphic portrayals of the data show either standard deviations (SD) or standard errors of the mean (SEM), as specified. Data analysis was performed using Prism (GraphPad Software, La Jolla, CA, USA), Excel (Microsoft, Redmond, WA, USA), FlowJo (Tree Star, Ashland, OR, USA), and ImageQuant (GE).
MSC/OBC direct contact cultures
To assess the osteogenic progression of MSCs cultured in direct contact with OBCs, RT-PCR and human osteogenesis Superarray analyses were performed on FACS-sorted MSCs that had been labeled with DiI and then co-cultured with OBCs while undergoing osteogenic differentiation. We first verified that the DiI labeling did not alter MSC gene expression or morphology (Additional file 2: Figure S1). Our results showed that in mixed co-cultures, no obvious morphological differences (Additional file 3: Figure S2) nor consistent changes in gene expression (Additional file 4: Figure S3) were seen (n = 5).
MSC Osteogenesis in OBC-Conditioned medium
To further characterize the nature of OBC-to-MSC signaling, MSCs were cultured in OM that had previously been conditioned by OBCs during days 11-14 of their osteogenic progression. MSC expression of OC, ALP, Col I and Runx2, as assayed by real time RT-PCR, was not significantly different in OBC-conditioned OM versus the AOM control (Additional file 5: Figure S4). None of the changes in gene expression were greater than 1.7-fold and none of them were statistically significant (n = 3). This was confirmed by AlzR histological staining of matrix mineralization and ALP histochemical staining (data not shown).
Mineralization of MSCs on OBC Matrix
Gene expression and morphology of MSCs on decellularized OBC matrix
To confirm these data and broaden the number of genes being assessed, we carried out real-time RT-PCR microarray analysis using human osteogenesis Superarrays (see Additional file 6: Figure S5.pdf). Changes ≥3-fold were analyzed. The trends seen previously in the four osteogenic markers (above) were somewhat altered, presumably due to donor variability. Changes in ALP and Runx2 levels did not reach three-fold, although ALP levels were reduced by more than two-fold on water-matrix on days 6 and 12 and on DOC-matrix on day 6. Runx2 levels decreased by 2.3-fold on DOC-matrix on day 6 but all other conditions elicited little change. Twenty-one genes related to osteogenesis displayed ≥3-fold changes in MSCs on matrix, including OC and Col I. All of them were down-regulated except CSF2, CSF3, ITGA2, OC and VEGFA. OC was up only on day 6 in MSCs on DOC-matrix. The down-regulated genes included BGN, BMP4, CD36, CDH11, COL1A1, COL1A2, COL4A3, COL10A1, COL11A1, COL12A1, COMP, FGFR2, ICAM1, IGF1, IGF2, and MMP8. Overall, while the Superarray data did not reflect the greater potency of water-treated matrix versus DOC-treated matrix, suppression of MSC osteogenesis by OBC matrix was confirmed.
Specificity of the effect of OBC-derived matrix
Finally, it should be noted that the observed effects of OBC matrix on MSC osteogenesis appeared to be OBC-specific. This was confirmed by comparing the effect of OBC matrix on MSC osteogenesis to that of matrix derived from human foreskin fibroblasts (HFF), prepared using an identical water lysis decellularization protocol. As shown in Additional file 7: Figure S6, HFF-derived matrix did not suppress the ALP level as effectively as OBC-derived matrix.
OBC matrix protein identification by 2D-DIGE
“Pick List” of statistically significant protein spots for identification
Identities of Proteins from "Pick List"
Entrez Gene Name
Found in Spots:
actin, alpha 2, smooth muscle, aorta
826, 894–6, 1053
aldehyde dehydrogenase 1 family, member B1
aldo-keto reductase family 1, member C1
ATP synthase, H+ transport, mitoch F1 complex, alpha 1
ATP synthase, H+ transport, mitoch F1 complex, beta
cytoskeleton-associated protein 4
enolase 1, alpha
enolase 3, beta, muscle
eukaryotic translation initiation factor 3, subunit B
heat schock protein 90kDa beta (Grp94), member 1
449, 636, 637
heat shock 27kDa protein 1
heat shock 60kDa protein 1 (chaperonin)
heat shock 70kDa protein 5 (glucose-regulated)
IKK interacting protein
prolyl 4-hydroxylase, beta polypeptide
201, 607, 636
proteasome (prosome, macropain) 26S subunit, 13
protein disulfide isomerase family A, member 3
protein disulfide isomerase family A, member 6
pyruvate dehydrogenase (lipoamide) beta
pyruvate kinase, muscle
superoxide dismutase 2, mitochondrial
tubulin, alpha 1A
collagen, type VI, alpha 1
201, 203, 208, 210, 224, 242, 247
collagen, type VI, alpha 3
247, 607, 649
EGF-containing fibulin-like ECM protein 2
elastin microfibril interfacer 1
224-6, 242, 247
HtrA serine peptidase 1
transforming growth factor, beta-induced, 68kDa
all but 1093-96
crystallin, alpha B
In this study, we have attempted to model the bone marrow niche of adult MSCs in vitro by generating a nascent osteoblast environment and testing its effect on MSC osteogenesis. When RT-PCR was used after FACS separation of cocultured MSCs, no differences were detected in osteogenic transcript levels between MSCs cultured with and without contact with OBCs. These results are corroborated by the findings of Wang et al.  in a similar study using mouse cells. These authors mixed MC3T3-E1 mouse osteoprogenitor cells with MSCs from GFP-transgenic mice, cultured them in OM at a plating density of 5,000/cm2 for 21 days, then FACS sorted the MSCs based on green fluorescent protein (GFP) fluorescence, and analyzed the transcript levels of osteogenic genes. Their results showed that direct cell-cell contact with the osteoblastic cells did not significantly alter the osteogenic differentiation of the MSCs.
As in our study, Wang et al.  also examined the effects of OB-secreted proteins on the osteogenesis of MSCs. When mouse MSCs were cultured indirectly with MC3T3 cells in OM using Transwell inserts, the proliferation of neither cell type was affected, but matrix calcification was enhanced and several osteogenic gene transcript levels were significantly increased. The differences in our results may be related to the developmental stage of the OBs used: the mouse MC3T3 osteogenic cell line is derived from newborn mouse calvaria, while the OBCs used here are recently derived from adult human MSCs. It is also known that mouse and human MSCs do not respond equivalently to all osteogenic stimuli . Additionally, other studies have also reported a lack of osteo-induction by OB-secreted factors. For example, Gerstenfeld et al.  found that C3H10T1/2 mouse embryonic MSCs did not increase their expression of OC when co-cultured in Transwells with chick embryonic calvarial OBs.
A number of studies have assessed the effects of various ECMs and their individual components on the osteogenic differentiation of mesenchymal cells [24, 25]. Although the experimental systems were usually simplified to examine the effects of a single ECM protein on MSC osteogenesis, many of the studies reported conflicting results. Shi et al.  found that Col I-coated plates stimulated Col I, ALP and osteopontin gene expression in rat neonatal calvarial cells (ROB-C26) without osteo-inductive medium, but the Col I matrix was not sufficient to induce ALP activity or the expression of TGF-α1, TGF-β2 or BMP-6. Salasznyk et al.  concluded similarly that human MSCs can be induced to differentiate into OBs through contact with Col I or vitronectin, without osteogenic supplements, as assessed via mineralization and Col I, OPN and ALP mRNA. Cool and Nurcombe , however, saw no differences in proliferation, ALP activity or Runx2, Col I or OC mRNA levels in murine MSCs seeded on Col I, FN1 or laminin substrates and cultured in OM. (Note: culturing in EM was not tested.) Nor did Heckmann et al.  observe an induction of OC or Col I expression when human MSCs were cultured on a three-dimensional Col I matrix. There is thus no obvious consensus in the literature regarding the effects of any single ECM protein on MSC osteogenesis.
While these apparent conflicts may be related to differences of species, substrates or culture media, these studies by their very nature are overly reductionistic in terms of mimicking the in vivo environment since the ECM is a complex mixture of multiple components, deposited in temporospatially specific configurations and proportions that are important for their biological activities. To better approximate the in vivo niche, we chose to examine the activity of the matrix laid down by nascent osteoblastic cells. The native configuration of the OBC ECM is preserved by keeping it on the original culture dishes, without decalcification, fixation, or extraction. In this context, it is instructive to review the classic work of Urist on demineralized bone matrix (DBM) . In Urist’s studies, adult human and rabbit bones were lyophilized and decalcified and implanted into various muscles and bone defects. The DBM induced new bone formation within the rings of decalcified matrix. However, a later study showed that the principal inducers responsible for DBM-induced osteogenesis were BMPs sequestered in the bone matrix . This was further verified by Becerra et al.  who found that DBM could also enhance MSC osteogenesis indirectly through Transwell inserts. The fundamental difference between DBM and the ECM used here is one of age and structure. As bone matures over time, growth factors, such as BMPs, are sequestered within the bone matrix, particularly in the mature trabecular and cortical bone, as new layers of ECM are deposited and mineralized. The new matrix used here, synthesized by nascent OBCs and grown on a two-dimensional surface, is less likely to entrap growth factors. It more closely mimics that laid down by bone-lining cells at the endosteal surface of the bone marrow cavity, i.e., it is similar to the osteoblastic matrix that MSCs likely encounter in vivo. Enhancement of MSC osteogenesis seen with mature bone matrix likely mimics what MSCs experience during fracture healing when trabecular or cortical bone is exposed along with its matrix and bound growth factors [31, 32]. MSCs, recruited to the site, thus come into contact with the growth factor-laden mature bone, which then induces them to begin osteogenic differentiation to repair the fracture.
One other study elegantly demonstrates the importance of the maturity of the OB matrix being studied . ECM was produced by neonatal rat calvarial cells (ROB-C26) cultured with or without retinoic acid, which induces osteogenesis in these cells. ECM made by the more osteoblastic cells was able to induce osteogenesis in naïve C26 cells in vitro and in vivo. However, ECM synthesized by C26 cells in the absence of retinoic acid was only able to partially stimulate osteogenesis in vitro and not at all in vivo.
Furthermore, Chen et al.  showed that ECM from murine MSCs themselves enhanced MSC proliferation and slowed their spontaneous osteogenic differentiation, while enhancing their tri-lineage plasticity. A second study confirms this in human MSCs and identifies several of the proteins present in the ECM (Col I, Col II, FN, byglycan, decorin, perlecan, and laminin) .
The fact that MSCs’ own matrix can help maintain their stemness  is particularly interesting, not only because of its implications for the MSC niche, but also because it suggests that “concentrations” of ECM are important. Because MSC ECM is always available to MSCs, if this contact were sufficient to maintain their stemness, they would have to halt production of ECM proteins and withdraw from their ECM before differentiating. While this could be one explanation, there could also be thresholds of MSC-ECM interactions that must be reached before certain effects occur. Indeed, a similar idea was proposed by Volloch and Olsen  regarding the effect that the “density” of integrin-binding sites within various matrices has on MSC differentiation.
In addition to these quantitative thresholds of interacting ECM, apparently achieved in the OBC matrix studied here, there are likely qualitative characteristics of the OBC matrix, i.e., specific components that are important for the control of the differentiation activities of MSCs. Therefore, we compared the protein compositions of the DOC- and water-lysed OBC matrices using 2D-DIGE. Eleven focus proteins were chosen because of their characterization as ECM or membrane proteins, which makes them most likely to be in contact with MSCs in vivo. These were FN1, COL6A1, COL6A3, ANXA1, ANXA2, ANXA6, HTRA1, flotillin (FLOT1), EMILIN1, EFEMP2, and TGFBI. Several of these proteins have already been implicated in stem cell functions or osteogenesis. FN1, for example, was found in the MSC ECM reported in the study mentioned above to suppress MSC osteogenesis . It has also been used to coat tissue culture dishes to enhance the proliferation and plasticity of a subpopulation of MSCs [5, 37]. ANXA1 and 2 are up-regulated in amputated tadpole tails undergoing regeneration . Interestingly, they were also both identified in a proteomic analysis of mouse embryonic fibroblasts, which are the feeder layers cells used to maintain embryonic stem cells in vitro .
TGFBI binds collagen types I, II and IV and is expressed in most tissues . It has been shown to be highly expressed in HSCs that adhere well to MSCs . This observation is significant because the binding of HSCs to MSCs has been implicated in the maintenance of the HSC phenotype in culture . In addition, when TGFBI is exogenously added to periodontal ligament cells, it can inhibit their mineralization, suggesting an anti-osteogenic function . Recent research shows that HTRA1 may play a similar role since it inhibited mineral deposition in immortalized murine OBs (2 T3 cells) even in the presence of BMP-2 . The same study also showed that its overexpression reduced levels of Runx2 and Col I mRNA. However, further research, using human MSCs, showed an opposite effect for HTRA1 , although it did confirm that HTRA1 secretion from MSCs increases as they undergo osteogenesis and, in mice, it is found mostly in areas of new bone formation after fracture.
EMILIN1 has not yet been linked to bone tissues but is known to bind pro-TGF-β, a key regulator of osteogenesis, in the extracellular space of blood vessels . This binding inhibits the maturation of TGF-β, the purpose of which may be the prevention of fibrosis due to Col I buildup .
To date, several studies have shown that ECMs generated by various cell types in vitro, including MSCs themselves, can encourage MSC stemness and suppress their differentiation [34, 47–50]. It is unlikely that there is a single MSC niche produced by a single cell type. Indeed MSCs are found throughout the body in various tissues. To discover which proteins are most important in maintaining and expanding MSCs, one approach would be to compare the proteins present in OBC ECM to those found in other stemness-enhancing ECMs. Since the ECM generated by MSCs of older mice has been shown to be less efficient in maintaining their stemness , we suggest that the protein makeup of ECMs from human donors of various ages be compared as well.
In summary, our study has shown an osteo-inhibitory function for OBC matrix laid down in vitro by nascent osteoblasts derived from osteogenically differentiated MSCs. The OBC matrix is likely to be similar to that laid down by newly-formed, active OBs that line the endosteal surface in the bone marrow milieu. Since only MSC osteogenesis is examined here, whether the “niche effect” seen is specific to osteogenesis only or applicable to the maintenance of MSC stemness in general remains to be investigated. In either case, it may be that MSCs in the marrow stroma are often in contact with similar nascent OB matrix and are thus kept in an undifferentiated state. In a traumatic bone injury setting, MSCs would be called forth to migrate from their niche to the site of fracture where they would come into contact with mature bone and its matrix, which would then act to stimulate their osteogenic differentiation via matrix-entrapped growth factors. This model, if proven correct, will strongly suggest that the OBC matrix and/or its active components may be applied in vitro to develop a means to extend the proliferative potency and therapeutic utility of MSCs by suppressing their default osteogenic differentiation.
We sincerely thank Dr. Paul Manner (University of Washington) for providing femoral head tissue samples, and Jim Simone (NIAMS Flow Cytometry Facility), Dr. Lewis Pannell (Proteomics and Mass Spectrometry Laboratory, University of South Alabama), and Roberto Diaz (GE) for countless hours of sample processing and procedural advice. Supported by the NIH Intramural Research Program (Z01 AR41131) and the Commonwealth of Pennsylvania Department of Health (SAP 4100050913).
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