TransTissue Technologies GmbH, Berlin, Germany.
J Orthop Res. 2010 Jun;28(6):819-27. doi: 10.1002/jor.21058.
In microfracture, subchondral progenitors enter the cartilage defect and form cartilage repair tissue. We hypothesize that synovial fluid (SF) from rheumatoid arthritis (RA) donors affects chondrogenesis of human subchondral progenitors stimulated with transforming growth factor-beta3 (TGFB3), whereas SF from normal and osteoarthritis (OA) donors do not. Human progenitors from subchondral cortico-spongious bone (pool of n = 4) were cultured in micromasses under serum-free conditions and were stimulated with 10 ng/mL TGFB3 and with 5% SF from normal, OA, and RA donors (pool of n = 7, each). Histological staining of proteoglycan and immunostaining of type II collagen showed that progenitors stimulated with SF from RA donors show significantly reduced cartilage matrix formation compared to progenitors treated with TGFB3 or with SF from normal and OA donors (n = 3, each). Gene expression analysis of typical chondrocyte marker genes and genes encoding matrix modifying enzymes showed that SF from OA and RA donors influence the onset of TGFB3-mediated chondrogenesis (pool of 20 micromasses), but had no effect on the gene expression profile after prolonged culture in micromasses. These results suggest that SF from RA patients may impair the chondrogenic development of mesenchymal progenitors in microfracture, whereas osteoarthritic SF may has no negative effect on the cartilage matrix formation.
在微骨折术中,软骨下祖细胞进入软骨缺陷并形成软骨修复组织。我们假设类风湿关节炎(RA)供体的滑液(SF)会影响转化生长因子-β3(TGFB3)刺激的人软骨下祖细胞的软骨生成,而正常和骨关节炎(OA)供体的 SF 则不会。在无血清条件下,将来自软骨下皮质海绵骨的人类祖细胞(n = 4)培养在微团中,并分别用 10ng/ml TGFB3 和来自正常、OA 和 RA 供体的 5%SF(n = 7,每组)刺激。蛋白聚糖的组织学染色和 II 型胶原的免疫染色表明,与用 TGFB3 或正常和 OA 供体的 SF 处理的祖细胞相比,用 RA 供体的 SF 刺激的祖细胞显示出明显减少的软骨基质形成(n = 3,每组)。典型软骨细胞标记基因和编码基质修饰酶的基因的表达分析表明,OA 和 RA 供体的 SF 影响 TGFB3 介导的软骨生成的起始(20 个微团的池),但对微团中延长培养后的基因表达谱没有影响。这些结果表明,RA 患者的 SF 可能会损害微骨折术中间充质祖细胞的软骨生成发育,而骨关节炎的 SF 可能对软骨基质形成没有负面影响。