Dr. Seol and Mr. McCabe contributed equally to this work.
Chondrogenic progenitor cells respond to cartilage injury
Article first published online: 27 OCT 2012
Copyright © 2012 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 64, Issue 11, pages 3626–3637, November 2012
How to Cite
Seol, D., McCabe, D. J., Choe, H., Zheng, H., Yu, Y., Jang, K., Walter, M. W., Lehman, A. D., Ding, L., Buckwalter, J. A. and Martin, J. A. (2012), Chondrogenic progenitor cells respond to cartilage injury. Arthritis & Rheumatism, 64: 3626–3637. doi: 10.1002/art.34613
- Issue published online: 27 OCT 2012
- Article first published online: 27 OCT 2012
- Accepted manuscript online: 6 JUL 2012 09:56AM EST
- Manuscript Accepted: 26 JUN 2012
- Manuscript Received: 30 SEP 2011
- US Department of Defense. Grant Number: W81XWH-10-1-0702a
- World Arthrosis Organization
- Top of page
- MATERIALS AND METHODS
- AUTHOR CONTRIBUTIONS
Hypocellularity resulting from chondrocyte death in the aftermath of mechanical injury is thought to contribute to posttraumatic osteoarthritis. However, we observed that nonviable areas in cartilage injured by blunt impact were repopulated within 7–14 days by cells that appeared to migrate from the surrounding matrix. The aim of this study was to assess our hypothesis that the migrating cell population included chondrogenic progenitor cells that were drawn to injured cartilage by alarmins.
Osteochondral explants obtained from mature cattle were injured by blunt impact or scratching, resulting in localized chondrocyte death. Injured sites were serially imaged by confocal microscopy, and migrating cells were evaluated for chondrogenic progenitor characteristics. Chemotaxis assays were used to measure the responses to chemokines, injury-conditioned medium, dead cell debris, and high mobility group box chromosomal protein 1 (HMGB-1).
Migrating cells were highly clonogenic and multipotent and expressed markers associated with chondrogenic progenitor cells. Compared with chondrocytes, these cells overexpressed genes involved in proliferation and migration and underexpressed cartilage matrix genes. They were more active than chondrocytes in chemotaxis assays and responded to cell lysates, conditioned medium, and HMGB-1. Glycyrrhizin, a chelator of HMGB-1 and a blocking antibody to receptor for advanced glycation end products (RAGE), inhibited responses to cell debris and conditioned medium and reduced the numbers of migrating cells on injured explants.
Injuries that caused chondrocyte death stimulated the emergence and homing of chondrogenic progenitor cells, in part via HMGB-1 release and RAGE-mediated chemotaxis. Their repopulation of the matrix could promote the repair of chondral damage that might otherwise contribute to progressive cartilage loss.
The risk of posttraumatic osteoarthritis (OA) after serious joint injuries is still as high as 70%, despite many refinements in care (1–3). This underscores the urgent need for new treatments to prevent articular cartilage loss initiated by joint damage and cartilage injury. Most macroscopic cartilage lesions do not heal and may spread locally or stimulate joint-wide cartilage degeneration (1, 4). This occurs despite the presence of potentially reparative chondrogenic progenitor cells in cartilage and other intraarticular tissue (5–8) that show vigorous in vitro chondrogenic activity. It may be possible to coax these cells to be more effective in vivo, but more complete knowledge of the posttraumatic behavior and function of chondrogenic progenitor cells is needed to evaluate this potential.
Like mesenchymal stem cells (MSCs) that originate in bone marrow, progenitor cells residing in tissue are multipotent, highly clonogenic, and chemotactic (9–11). Progenitor cells migrate locally to sites of injury, where they proliferate and differentiate as needed to replace damaged tissue (12, 13). Unlike MSCs, which must be capable of differentiating suitably for the regeneration of multiple tissues in different organ systems, progenitor cells do not require such pluripotency for local tissue regeneration, and the repertoire of progenitor cells is typically more limited than that of MSCs (12).
Chondrogenic progenitor cells were first identified in calf cartilage as a subpopulation of superficial zone cells required for the appositional growth of articular cartilage (5, 14). This specialized cell population was isolated from other cartilage cells based on enhanced binding to fibronectin. Compared with normal chondrocytes, chondrogenic progenitor cells overexpressed the stem cell–associated factor Notch-1 and the fibronectin receptor α5β1 integrin. The cells also showed enhanced clonality in culture and multipotency when grafted to chick limb buds. Alsalameh et al (15) subsequently showed that ∼4% of cells in normal human cartilage expressed the MSC markers CD105 and CD166. This frequency increased to almost 8% in OA cartilage. However, less than half of the CD105+CD166+ cells were capable of adipogenic differentiation, suggesting that CD marker status overestimated the numbers of multipotent MSC-like progenitor cells.
Using fluorescence-activated cell sorting analysis, Hattori et al demonstrated that 0.07% of cells present in the superficial zone of calf stifle cartilage were capable of Hoechst 33342 dye exclusion, whereas none of the cells from the middle or deep zones excluded the dye (7). Because expression of the multidrug transporter responsible for dye exclusion is typical of stem cells (16), the authors concluded that they had identified a stem-like progenitor cell population. A subpopulation of CD13-, CD29-, CD44-, CD73-, CD90-, and CD105-expressing cells was observed in repair tissue in OA cartilage obtained at the time of total joint replacement. The cells appeared to migrate from subchondral bone via tidemark-spanning blood vessels and expressed both the osteoblastic transcription factor runt-related transcription factor 2 (RUNX-2) and the chondrogenic transcription factor SOX9 (8, 17). Concurrently, Grogan and coworkers (6) observed high numbers of chondrocytes (>45%) that were immunohistologically positive for the MSC markers Notch-1 and STRO-1 in both normal and OA cartilage. These cells were osteogenic and chondrogenic but not adipogenic, and they included a small side population (0.14%) of Hoechst dye–excluding cells.
Necrotic cell death associated with wounding releases intracellular components that serve as chemotactic signals for progenitor cells, stem cells, and leukocytes. Known collectively as “alarmins” or damage-associated molecular pattern molecules, they include mitochondrial DNA and formyl methionine–containing peptides and DNA-binding high mobility group proteins such as high mobility group box chromosomal protein 1 (HMGB-1) and HMGB-2 and multiple S100 proteins (18–21). Alarmin binding to receptor for advanced glycation end products (RAGE) and Toll-like receptors stimulates the migration of progenitor cells and stem cells, attracting them to injury sites, where they participate in tissue regeneration and repair (22–25). The potent antiinflammatory drug glycyrrhizic acid (glycyrrhizin) is a natural product derived from licorice that binds HMGB-1 and blocks its activities (26). Additional chemotactic recruitment is stimulated by CXC ligands (CXCLs) released by tissue and inflammatory cells (27, 28). Several studies have shown that blunt trauma to articular cartilage induces acute chondrocyte necrosis and apoptosis (1, 29–35). In an explant trauma model, we observed cells migrating over cartilage surfaces near sites of extensive chondrocyte death. These cells were isolated and evaluated for progenitor cell characteristics and chemotactic responses to injury-related alarmins.
MATERIALS AND METHODS
- Top of page
- MATERIALS AND METHODS
- AUTHOR CONTRIBUTIONS
Explant harvest and culture.
Stifle joints from young adult cattle (15–24 months old) were obtained from a local abattoir (Bud's Custom Meats). Osteochondral explants were prepared by manually sawing an ∼25 × 25-mm portion of the bovine tibial plateau that included the central loaded area of the articular surface. After obtaining institutional review board approval, osteochondral explants from 3 normal tali of patients undergoing lower limb amputation for cancer were obtained and prepared in the same manner. The patients were males ages 29, 34, and 46 years who did not have a diagnosis of OA. The explants were rinsed in Hanks' balanced salt solution (HBSS) and cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (Invitrogen Life Technologies), 50 μg/ml L-ascorbate, 100 units/ml penicillin, 100 μg/ml streptomycin, and 2.5 μg/ml Fungizone.
After 2 days in culture, the human and bovine explants were injured by blunt impact (14 J/cm2) via a 5-mm–diameter flat-ended platen, using a drop tower device as described previously (35, 36). In some cases, explant cartilage was dissected free from subchondral bone immediately after impact injury. Scratch injuries were made by dragging a 26-gauge needle over the cartilage surface to create X-shaped matrix tears of ∼0.5 mm in depth. Confocal imaging studies were performed essentially as previously described (35, 36). Briefly, explants were stained with calcein AM (viability) and ethidium homodimer (dead cells) and submerged in culture medium. After a 30-minute incubation, the explants were imaged using a Bio-Rad 1024 confocal laser scanning microscope.
Five to seven days after injury, the explants were submerged in 0.25% trypsin–EDTA in HBSS and incubated for 10 minutes to detach migrating progenitor cells from the surface. Imaging studies performed before and after submersion in trypsin confirmed that the brief enzymatic treatment removed the surface-adherent migrating cells without disrupting the underlying superficial chondrocytes. To recover normal chondrocytes, the underlying cartilage was digested overnight with type I collagenase and Pronase E (Sigma-Aldrich) dissolved in culture medium (0.25 mg/ml each). A custom-fabricated device was used to separate the superficial one-third and lower two-thirds zones of the cartilage sample prior to collagenase/Pronase digestion. Colony-forming assays were performed as previously described (37).
Green fluorescent protein labeling.
For some experiments, isolated putative chondrogenic progenitor cells were labeled with green fluorescent protein (GFP; 488 nm) by lentiviral transduction. GFP-labeled cells (1 × 105) were suspended in chilled (8°C) hydrogel consisting of 0.6% 2-kd hyaluronic acid (Easy Motion Horse) and 18% Pluronic F-127 (Sigma-Aldrich) in normal saline. Pluronic F-127 is a polyol surfactant that confers temperature-sensitive gelation to solutions (38). The cold suspension gelled on contact with warmed (37°C) explants, such that the suspended cells were held in place adjacent to a site of blunt impact. The explants were incubated for 5 days, after which they were counterstained with 0.5 μM CellTracker Red CMTPX (Invitrogen Life Technologies) and imaged using a Bio-Rad 1024 confocal microscope with a custom-built XY microscope stage driver (Condensed Matter Sciences Division). The sites were scanned to an average depth of 330 μm at 40-μm intervals. Z-axis projections of confocal images were obtained using ImageJ (rsb.info.nih.gov/ij).
Immunofluorescence staining for proliferating cell nuclear antigen (PCNA) was performed on paraformaldehyde-fixed cryosections of cartilage from 3 different explants that had been cultured for 10 days after an impact injury, using an anti-PCNA monoclonal antibody (Abcam); an Alexa Fluor 488–labeled goat anti-mouse secondary antibody (Jackson ImmunoResearch) was used for detection. The sections were mounted in Vectashield mounting medium, using DAPI (Vector) to stain nuclei. Additional sections from the same explants were stained with Safranin O–fast green to reveal tissue morphology. Proteoglycin 4 (PRG4; lubricin) immunohistochemical analysis was performed on sections from the same specimens, using a mouse monoclonal antibody (MD Biosciences) and a Vectastain ABC kit (Vector). Transmitted light images and epifluorescence images were obtained using a QImage CCD camera (QImaging) mounted on an Olympus BX60 microscope.
Cell migration/chemotaxis assays.
Cell migration/chemotaxis assays were performed using a CytoSelect 24-Well Cell Invasion Assay kit (Cell Biolabs) essentially as described by the manufacturer. Putative chondrogenic progenitor cell or normal chondrocyte suspensions (3 × 105 cells in serum-free medium) were added to the upper Transwell and placed in reservoirs containing serum-free medium alone or serum-free medium with various chemokines, cell lysates, or serum-free medium conditioned by injured explants. The plates were incubated for 24 hours prior to processing. Cell lysates were transferred to fluorescence plates and read on a microplate reader (Molecular Devices). The data are presented as the percentage of migrating cells ([number of cells in the bottom chamber/number of cells seeded] × 100).
Conditioned medium was made by incubating blunt-impacted explants overnight in 10 ml of serum-free medium. The medium was concentrated 10-fold using Amicon Ultra centrifugal 10K filters (Millipore). Lysates for testing in the chemotaxis assay were obtained by repeated freeze-thawing of cells from primary cultures of bovine chondrocytes isolated from distal femurs. Glycyrrhizic acid (Sigma-Aldrich) and a rabbit polyclonal anti-RAGE antibody (Abcam) were added to culture medium at a concentration of 25 μM (39). Porcine platelet–derived growth factor (PDGF BB; R&D Systems) was diluted in medium to a concentration of 300 nM (40). The effects of glycyrrhizic acid and anti-RAGE antibody on migration in the explant model were assessed by confocal microscopy and by counting the number of migrating cells harvested from explant surfaces by trypsinization 14 days after blunt impact. The explants (n = 4/group) were treated daily starting immediately after impact.
Side population assay.
Side population assays were performed essentially as previously described (7). First-passage putative chondrogenic progenitor cells and normal chondrocytes in suspension in HBSS (1 × 106/ml) were incubated at 37°C for 1.5 hours with 2.5 mg/ml of Hoechst 33342 (Sigma-Aldrich), with or without 5 mM verapamil (Sigma-Aldrich). The cells were washed in cold HBSS, filtered through a 70-μm nylon mesh, and counterstained with propidium iodide to identify dead cells. Flow cytometric analysis was performed using a BD LSR II flow cytometer with an ultraviolet laser (BD Biosciences).
The multipotency of putative chondrogenic progenitor cells was tested by culturing them under chondrogenic, osteogenic, and adipogenic conditions (41). For chondrogenic differentiation, 1.2 million cells were pelleted and incubated in chondrogenic medium (DMEM containing 10 ng/ml transforming growth factor β1, 0.1 μM dexamethasone, 25 μg/ml L-ascorbate, 100 μg/ml pyruvate, 50 mg/ml ITS+ Premix, and antibiotics) for 14 days. The pellets were analyzed for matrix formation, using Safranin O–fast green staining of cryosections. To induce osteogenic differentiation, 3 × 104 trypsinized migrating cells were cultured in osteogenic medium (DMEM–Ham's F-12 containing 0.1 μM dexamethasone, 100 mM β-glycerophosphate, 50 μg/ml L-ascorbate, and antibiotics) for 14 days and stained with alizarin red to detect calcium phosphate mineralization. An adipogenesis differentiation kit (Gibco) was used to induce adipogenesis, and the cells were stained with oil red O 14 days postinduction. All cultures were imaged on a Nikon CX2 inverted microscope.
For microarray analysis, RNA was isolated from primary cultures of bovine MSCs, from freshly harvested putative chondrogenic progenitor cells, and directly from explant cartilage. Saline lavage was used to isolate MSCs from the marrow and subchondral bone of adult bovine tibiae. The lavage fluid was centrifuged, and the pelleted cells were plated in plastic dishes. Adherent cells were cultured for 5 days before harvesting. RNA was harvested from 3 independent batches of cells/explants. Cells and cartilage were homogenized in TRIzol reagent (Invitrogen Life Technologies), and total RNA was extracted using an RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. RNA (50 ng) was converted to single primer isothermal amplification–amplified complementary DNA (cDNA) using an Ovation RNA Amplification System version 2 (NuGEN). Biotinylated cDNA was placed onto Bovine Genome Arrays (Affymetrix). Arrays were scanned with an Affymetrix Model 3000, and data were collected using GeneChip operating software (MAS 5.0). Statistical analysis of the data was performed by one-way analysis of variance (ANOVA), and a heatmap and dendrogram were generated using Partek Genomics Suite software.
Previously published work indicated that progenitor cells can be distinguished from normal chondrocytes based on up-regulation of genes expressed in MSC populations (5, 6). These genes include ATP-binding cassette subfamily G member 2 (ABCG2), various CD cell markers, fetal liver kinase 1 (FLK-1), RUNX-2, and SOX9. Beta-actin was used for normalization. Real-time polymerase chain reaction (PCR) was performed to compare the expression of these markers in putative chondrogenic progenitor cells and normal chondrocytes, essentially as previously described (42).
Primers were purchased from Integrated DNA Technologies. The following primer sequences were used: for ABCG2, forward CCTTGGTTGTCATGGCTTCA and reverse AGTCCTGGGCAGAAGTTTTGTC; for CD105, forward CCACTGCCCCAGAGACTGCGC and reverse CCCCCACAGTGAGTGCTTAGGT; for CD90, forward CGGTGGTGTTTGGCCATGTAATGA and reverse GAGAGAGGGGAGTCCTATCCTGGT; for CD73, forward AGCTTTCCCAGCCTTCCATGCG and reverse GGGTGTCCTCTTGAGTCCTGCA; for CD39, forward CCACCCTCTCCTTCCGAGAGG and reverse TGACTGTAACCCTGGAGCTTGGCT; for CD29, forward GCGGCCTCCGGGTGGATTCC and reverse GCCGGGAAGGTCCAGGGGC; for FLK-1, forward TTCCAAGTGGCTAAGGGCAT and reverse TTTAACCACGTTCTTTTCCGACA; for RUNX-2, forward GCATGAAGCCCTATCCAGAGTCT and reverse GCTGATGGAGCTGTTGGTGTAG; for SOX9, forward CGGTGGTGTTTGGCCATGTAATGA and reverse GAGAGAGGGGAGTCCTATCCTGGT; for β-actin, forward TCGACACCGCAACCAGTTCGC and reverse CATGCCGGAGCCGTTGTCGA.
For colony-formation assays, statistical analysis was performed using SPSS software (version 10.0.7) with one-way ANOVA and post hoc pairwise comparison. Flow cytometry data (side population) were evaluated by Student's t-test. One-way and two-way ANOVAs with the Holm-Sidak post hoc test were used to analyze migration assay data. Results are presented as the mean ± SD.
- Top of page
- MATERIALS AND METHODS
- AUTHOR CONTRIBUTIONS
Blunt impact injury to explant surfaces caused local chondrocyte death and stimulated the emergence of migratory cells in and around impact sites. These cells began to accumulate 5 days after impact and gradually repopulated previously uninhabited areas (Figures 1A–C). Migrating cells were morphologically distinct from normal chondrocytes in that they were elongated with multiple thin cytoplasmic extensions (Figure 1D). A similar migratory reaction was observed at impact sites in explanted human tali (Figures 1E and F) and in a scratch injury (Figures 1G and H). Migrating cells were also observed on impacted explant cartilage cultured without subchondral bone (Figure 1I). Immunostaining of cryosections from impacted explants revealed that surface-migrating putative chondrogenic progenitor cells were positive for PCNA, whereas chondrocytes beneath the surface were largely negative (Figure 1J). Surface putative chondrogenic progenitor cells were also strongly positive for lubricin (Figure 1K).
Five to seven days after impact injury, surface-adherent migrating cells were detached from the injured explants by trypsin treatment. Some cells were transduced with GFP and grafted ∼4 mm away from a freshly made impact site on another explant (Figure 2A). The number of labeled cells in the impact site increased dramatically from day 2 to day 12 (Figures 2B–D). The clonogenic activity of trypsinized cells was compared with that of chondrocytes from the upper one-third of the cartilage, which included the superficial and transitional zones, and from the bottom two-thirds, which included the transitional and deep zones (Figure 3). Primary cultures were established, and the cells were harvested after 5–7 days in culture for colony-formation assays. Trypsinized cells in monolayer culture grew more rapidly than did chondrocytes (Figures 3A–D). These cultures were passaged, seeded in cloning dishes, and incubated for 10 days. Trypsinized cells showed the most vigorous colony formation in terms of both the total number of colonies and the average colony size (Figures 3E–G). Trypsinized cells and chondrocytes from the upper one-third of the cartilage matrix showed significantly higher numbers of colonies (150 and 120, respectively) compared with chondrocytes from the bottom two-thirds of the matrix (20 colonies) (P = 0.001). The average colony size of trypsinized cells (20 mm2) was significantly greater than that of chondrocytes from the upper one-third or lower two-thirds of the matrix, both of which showed average colony sizes of <5 mm2 (P = 0.001). However, ∼1% of the colonies formed by chondrocytes from the upper one-third of the matrix showed areas of ≥20 mm2.
Putative chondrogenic progenitor cells were cultured in chondrogenic, osteogenic, or adipogenic medium for 14 days in order to evaluate their differentiation potential. After the induction of chondrogenic differentiation, cultured pellets were fixed and stained with Safranin O–fast green, revealing a proteoglycan-rich matrix throughout the pellets (Figure 4A). Similarly, most cells in osteogenic medium deposited a calcium phosphate–rich mineralized matrix, as detected by alizarin red staining (Figure 4B). However, few cells (<1%) stained with oil red O after 2 weeks of culture in adipogenic medium (Figure 4C).
Flow cytometric analysis of Hoechst 33342–stained normal chondrocytes revealed few side population cells (mean ± SD 0.032 ± 0.012%) (Figure 4D). The side population was significantly larger in trypsinized cells (0.22 ± 0.07%; P = 0.001). Verapamil treatment reduced side populations to <0.005%, indicating that stain efflux depended on the stem cell–associated ABCG2 transporter. Real-time PCR analysis revealed substantially higher expression of stem cell marker genes in putative chondrogenic progenitor cells compared with normal chondrocytes (Figure 4E). ABCG2 expression was increased by >4-fold, SOX9 expression was increased by 3.8-fold, and FLK-1 expression was increased by 2.8-fold. CD105, CD73, CD39, and CD29 expression was increased by <2-fold in putative chondrogenic progenitor cells, and CD90 expression was 2-fold higher in normal chondrocytes than in putative chondrogenic progenitor cells. Microarray analysis showed elevated expression of the progenitor cell markers Notch-1 (7.4-fold) and CD44 (12-fold) in putative chondrogenic progenitor cells compared with normal chondrocytes.
Statistical analysis of microarrays indicated that overall gene expression in putative chondrogenic progenitor cells was more similar to that of MSCs than to that of normal chondrocytes (Figure 4F). Individual genes that showed statistically significant differences (P < 0.05) in expression of >2-fold in putative chondrogenic progenitor cells versus normal chondrocytes or MSCs are listed in Table 1. The listed genes were selected for relevance to inflammation, proliferation, migration, and chondrogenic differentiation. The proinflammatory cytokine interleukin-6 (IL-6) was among the most highly up-regulated genes in chondrogenic progenitor cells compared with normal chondrocytes (130-fold increase). Chemokines involved in stem cell and leukocyte chemotaxis (28, 43) were also strikingly up-regulated in putative chondrogenic progenitor cells relative to normal chondrocytes: CXCL12 expression was >25-fold greater, and CXCL8 (IL-8) expression was increased by >35-fold. Also relative to normal chondrocytes, matrix metalloproteinase 1 (MMP-1) and MMP-13 genes were overexpressed in putative chondrogenic progenitor cells by 18-fold and 4.3-fold, respectively, and the proliferation-related cyclin B1 and cyclin D1 genes were overexpressed by 35-fold and 9-fold, respectively. Genes encoding the cartilage extracellular matrix components type X collagen (COL10A1), type IX collagen (COL9A2), type II collagen (COL2A1), aggrecan (ACAN), and cartilage oligomeric matrix protein (COMP) were among the most down-regulated genes in putative chondrogenic progenitor cells.
|CPCs vs. NCs|
|IL6||130||3.6 × 10−5|
|DOCK10||62||4.4 × 10−7|
|CXCL8||36||3.0 × 10−3|
|CCNB1||35||5.8 × 10−5|
|CXCL12||28||2.4 × 10−5|
|CSF1||21||9.3 × 10−6|
|MMP1||18||3.9 × 10−3|
|CD44||12||6.1 × 10−3|
|ADAMTS4||10||2.9 × 10−5|
|IL1RN||9.1||1.3 × 10−4|
|CCND1||9.0||2.3 × 10−5|
|NOTCH1||7.4||9.4 × 10−7|
|ADAM9||6.4||1.6 × 10−3|
|IGFBP3||5.6||2.7 × 10−2|
|MMP13||4.3||1.2 × 10−2|
|HMMR||4.2||1.4 × 10−4|
|TLR3||3.7||3.7 × 10−2|
|ITGB5||3.6||4.0 × 10−2|
|COL6A1||3.1||1.1 × 10−2|
|ADAM8||3.0||2.0 × 10−2|
|COL10A1||−192||7.0 × 10−6|
|CHAD||−136||1.5 × 10−8|
|COL9A2||−38||4.9 × 10−6|
|COL2A1||−12||9.8 × 10−6|
|TIMP4||−8.3||9.4 × 10−5|
|ACAN||−8.0||5.2 × 10−3|
|INSR||−6.0||1.7 × 10−3|
|COMP||−5.4||4.9 × 10−4|
|TIMP4||−4.8||9.7 × 10−4|
|FGF2||−3.9||3.2 × 10−4|
|ACAN||−3.7||3.2 × 10−2|
|PTH1R||−3.1||1.8 × 10−2|
|DNMT3A||−2.9||2.3 × 10−2|
|CPCs vs. MSCs|
|PRG4||78||7.6 × 10−5|
|MMP3||23||1.0 × 10−3|
|ACAN||17||5.4 × 10−4|
|S100A1||16||2.7 × 10−4|
|MMP1||15||5.2 × 10−3|
|HAPLN1||13||1.0 × 10−5|
|CXCL2||12||2.0 × 10−2|
|IL8||10||2.5 × 10−2|
|COL2A1||6.9||8.0 × 10−5|
|SOD3||6.7||1.3 × 10−4|
|COL5A3||6.2||1.5 × 10−3|
|FGF2||5.1||8.6 × 10−5|
|IL16||3.3||8.5 × 10−3|
|CD83||3.2||1.5 × 10−2|
|PLAT||3.0||4.2 × 10−2|
|SOCS1||2.7||2.2 × 10−2|
|IL1A||2.7||2.2 × 10−2|
|S100B||2.6||1.6 × 10−3|
|PDGFRA||2.5||8.4 × 10−3|
|SOD2||2.3||3.4 × 10−2|
|NID1||−11||4.4 × 10−2|
|IGFBP7||−10||6.7 × 10−3|
|PPARG||−9.8||5.3 × 10−3|
|THBS1||−6.5||4.2 × 10−2|
|GPC4||−6.2||1.8 × 10−2|
|IGFBP3||−5.4||4.6 × 10−2|
|IGFBP2||−3.6||1.0 × 10−2|
|IL1RN||−3.6||4.3 × 10−3|
|PLAU||−3.0||2.0 × 10−3|
|DNMT3A||−2.7||1.1 × 10−2|
|IGFBP4||−2.6||2.6 × 10−2|
|NOTCH1||−2.3||6.2 × 10−4|
However, compared with MSCs, putative chondrogenic progenitor cells overexpressed the superficial chondrocyte marker PRG4 (lubricin) and the chondrocyte-associated genes S100A1 (16-fold) and S100B (2.6-fold). Moreover, ACAN and COL2A1 expression was much higher in putative chondrogenic progenitor cells than in MSCs (17-fold and 6.9-fold increases, respectively). In contrast, expression of the IL-1 receptor antagonist gene (IL1RN) was substantially down-regulated in putative chondrogenic progenitor cells compared with MSCs (−3.6-fold), as was the expression of several insulin-like growth factor binding proteins, including IGFBP7 (−10-fold), IGFBP3 (−5.4-fold), and IGFBP2 (−3.6-fold).
In general, putative chondrogenic progenitor cells were significantly more active in Transwell chemotaxis assays than were normal chondrocytes (P = 0.001); however, this was chemotactic factor dependent (Figure 5A). Compared with untreated control medium, CXCL12 significantly increased putative chondrogenic progenitor cell chemotaxis (P = 0.001) but had no effect on normal chondrocytes (P = 0.411). Neither putative chondrogenic progenitor cells nor normal chondrocytes responded to CXCL8 (P = 0.128 and P = 0.912, respectively), but conditioned medium from impact-injured explants induced chemotaxis to a similar degree in both putative chondrogenic progenitor cells and normal chondrocytes (P = 0.001). The response to cell lysates was significant for putative chondrogenic progenitor cells and normal chondrocytes (P = 0.001), but the putative chondrogenic progenitor cell response was significantly greater than the normal chondrocyte response (P = 0.001).
In addition to cell lysates and conditioned medium, putative chondrogenic progenitor cells responded strongly to purified HMGB-1 (Figure 5B). HMGB-1 at 10 nM or 20 nM significantly enhanced chemotaxis compared with controls (P = 0.001). The stimulatory effects of 10 nM HMGB-1 and the effects of conditioned medium and cell lysates were significantly suppressed by glycyrrhizin and by an anti-RAGE antibody (P = 0.001). The migratory activity stimulated by lysates, conditioned medium, and 10 nM HMGB-1 was similar to the activity stimulated by PDGF (250 nM), a well-known stem cell chemotactic factor. Glycyrrhizin and anti-RAGE antibody also significantly inhibited putative chondrogenic progenitor cell migration in impacted explants (P = 0.016 and P = 0.011, respectively) (Figure 5C).
- Top of page
- MATERIALS AND METHODS
- AUTHOR CONTRIBUTIONS
The results of these experiments demonstrated that the migrating cells we observed on injured bovine osteochondral explants closely resembled chondrogenic progenitor cells previously identified in normal and human OA cartilage. The chemotactic activity, clonogenicity, limited multipotency, and side population of the cells were all notably consistent with published descriptions of progenitor cells from cartilage and other tissue (6, 8, 14, 15, 17).
In vitro chemotaxis assays confirmed that media conditioned by impacted cartilage or cell lysates were relatively strong chemoattractants for putative chondrogenic progenitor cells. Furthermore, a scratch injury that caused localized chondrocyte death much like that observed in impact sites provoked the same response as impact injury, indicating that chondrocyte death was the main cause of putative chondrogenic progenitor cell activation in this system. The strong blocking effects of glycyrrhizin in the migration assays implicated the nuclear protein HMGB-1 as a primary chemoattractant in these complex mixtures. A blocking antibody to the RAGE receptor also significantly diminished migration, indicating that the effects of HMGB-1 were mediated in part by RAGE. The inhibitory effects of glycyrrhizin and anti-RAGE on putative chondrogenic progenitor cell migration/proliferation in the explant system were also significant; however, the treatments were less potent than those used in Transwell migration assays, suggesting that other factors contributed to the chemotactic activity. Indeed, our data suggested that PDGF might play such a role. A similar migratory response was observed in explanted human tali specimens with the same impact injuries as those in bovine explants, indicating that putative chondrogenic progenitor cell activation was not unique to the bovine system.
Putative chondrogenic progenitor cells appeared after injury when cartilage was cultured separately from subchondral bone. Cell populations derived from the top one-third of the cartilage matrix consistently yielded a few colonies that were as large as those formed by putative chondrogenic progenitor cells, whereas cells from the bottom two-thirds of the matrix never formed such colonies. Moreover, PRG4, which is expressed at high levels by superficial chondrocytes, was one of the most highly up-regulated genes in putative chondrogenic progenitor cells relative to MSCs. These findings strongly suggest that putative chondrogenic progenitor cells resided in the superficial zone before cartilage injury.
Compared with normal chondrocytes, putative chondrogenic progenitor cells overexpressed a few (but not all) stem cell–associated markers. Although ABCG2, RUNX2, and NOTCH1 expression was increased by ≥4-fold in putative chondrogenic progenitor cells, increases in CD markers were minor (<2-fold) and were not likely to be biologically significant. These results are mainly consistent with those of previous studies (5, 7, 15, 17), but the lack of substantive increases in CD marker expression suggests that the putative chondrogenic progenitor cells studied here might differ from progenitor cells of subchondral origin that more clearly overexpress these markers (17). Relative to normal chondrocytes, chondrogenic progenitor cells underexpressed chondrocyte-associated genes such as COL2A1 and ACAN. However, compared with MSCs, putative chondrogenic progenitor cells overexpressed COL2A1, ACAN, PRG4, S100A1, and S100B, all of which are considered to be chondrocyte markers (44). Thus, although they closely resembled MSCs in their overall pattern of gene expression, putative chondrogenic progenitor cells retained some chondrocyte-like features and were distinguishable from MSCs on that basis.
The expression of several metalloproteinases (MMP1, MMP13, ADAMTS4, ADAM8, and ADAM9) was significantly higher in putative chondrogenic progenitor cells than in normal chondrocytes. This was consistent with the enhanced chemotactic activity of putative chondrogenic progenitor cells compared with normal chondrocytes observed in our Transwell-based assays, which measured movement through a collagen matrix. With the notable exceptions of MMP1 and MMP13, the expression of which was up-regulated by >4-fold in putative chondrogenic progenitor cells, metalloproteinases were expressed at similar levels by MSCs, whose physiologic functions include migration through extracellular matrices.
The accumulation of hundreds of putative chondrogenic progenitor cells at injury sites was unlikely to be attributable solely to migration from the surrounding matrix. Putative chondrogenic progenitor cells grew rapidly in culture, and proliferation on cartilage surfaces is likely to explain the rapid repopulation of impact sites in the explant model. This was corroborated by immunofluorescence staining, which identified relatively high numbers of PCNA-positive cells among surface-migrating cells. Consistent with their highly clonogenic, proliferative phenotype, both MSCs and putative chondrogenic progenitor cells significantly overexpressed colony-stimulating factors, cyclins, and other growth-related genes.
The circumstances of the explant experiment dictated that we use different techniques to harvest RNA from chondrogenic progenitor cells and from normal chondrocytes. Thus, chondrogenic progenitor cell RNA was obtained from cells freshly removed from explant surfaces by trypsinization, normal chondrocyte RNA was extracted directly from cartilage, and MSC RNA was obtained from primary monolayer cultures. Although the trypsin treatment of chondrogenic progenitor cells was brief (∼10 minutes), it might have led to changes in the expression of some early-response genes. Moreover, procedural losses associated with RNA extraction from cartilage might have contributed to variability among the normal chondrocyte samples, which was higher than that in putative chondrogenic progenitor cell or MSC samples. Last, the effects of isolation and short-term culture on MSC gene expression are unknown and might have affected many of the genes that appeared to be differentially regulated compared with putative chondrogenic progenitor cells and normal chondrocytes.
The physiologic functions of chondrogenic progenitor cells and their effects on healing in injured joints remain unknown. Although chondrogenic progenitor cells efficiently repopulated damaged cartilage in our model, their relatively high levels of chemokine and cytokine expression and excessive metalloproteinase production could contribute to synovitis and cartilage degeneration in injured joints. In contrast, chondrogenic progenitor cells may be involved in the early stages of cartilage repair: confocal studies and histology showed that putative chondrogenic progenitor cells formed a continuous sheet over injured cartilage surfaces after ≥1 week in culture. The relatively high level of PRG4 expression by chondrogenic progenitor cells observed at the RNA and protein levels suggests that they help to restore the surface-protective lubricant coating on damaged cartilage, a process that may be involved in the repair of superficial defects (1, 45–49). The identification of HMGB-1 as an activator suggests a method to control chondrogenic progenitor cell responses to promote healing. Whether the goal should be to thwart or augment these responses will likely be decided by findings from in vivo models, in which treatments can be evaluated in a more physiologic setting.
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All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be published. Dr. Martin had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study conception and design. Seol, McCabe, Buckwalter, Martin.
Acquisition of data. Seol, McCabe, Choe, Zheng, Yu, Jang, Walter, Lehman, Ding.
Analysis and interpretation of data. Seol, McCabe, Martin.
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We thank Dr. Tae-Hong Lim for providing his hydrogel formulation, Dr. Prem S. Ramakrishnan for developing a cartilage dissection jig, and Sean M. Martin for his indispensible help with migration assays.
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