Nishida Takashi, Kubota Satoshi, Nakanishi Tohru, Kuboki Takuo, Yosimichi Gen, Kondo Seiji, Takigawa Masaharu
Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.
J Cell Physiol. 2002 Jul;192(1):55-63. doi: 10.1002/jcp.10113.
We previously reported that connective tissue growth factor/hypertrophic chondrocyte-specific gene product 24 (CTGF/Hcs24) stimulated the proliferation and differentiation of rabbit growth cartilage (RGC) cells in vitro. In this study, we investigated the effects of CTGF/Hcs24 on the proliferation and differentiation of rabbit articular cartilage (RAC) cells in vitro. RAC cells transduced by recombinant adenoviruses generating mRNA for CTGF/Hcs24 synthesized more proteoglycan than the control cells. Also, treatment of RAC cells with recombinant CTGF/Hcs24 (rCTGF/Hcs24) increased DNA and proteoglycan syntheses in a dose-dependent manner. Northern blot analysis revealed that the rCTGF/Hcs24 stimulated the gene expression of type II collagen and aggrecan core protein, which are markers of chondrocyte maturation, in both RGC and RAC cells. However, the gene expression of type X collagen, a marker of hypertrophic chondrocytes, was stimulated by rCTGF/Hcs24 only in RGC cells, but not in RAC cells. Oppositely, gene expression of tenascin-C, a marker of articular chondrocytes, was stimulated by rCTGF/Hcs24 in RAC cells, but not in RGC cells. Moreover, rCTGF/Hcs24 effectively increased both alkaline phosphatase (ALPase) activity and matrix calcification of RGC cells, but not of RAC cells. These results indicate that CTGF/Hcs24 promotes the proliferation and differentiation of articular chondrocytes, but does not promote their hypertrophy or calcification. Taken together, the data show that CTGF/Hcs24 is a direct growth and differentiation factor for articular cartilage, and suggest that it may be useful for the repair of articular cartilage.
我们之前报道过,结缔组织生长因子/肥大软骨细胞特异性基因产物24(CTGF/Hcs24)在体外可刺激兔生长软骨(RGC)细胞的增殖和分化。在本研究中,我们调查了CTGF/Hcs24对兔关节软骨(RAC)细胞体外增殖和分化的影响。用产生CTGF/Hcs24 mRNA的重组腺病毒转导的RAC细胞比对照细胞合成了更多的蛋白聚糖。此外,用重组CTGF/Hcs24(rCTGF/Hcs24)处理RAC细胞可使DNA和蛋白聚糖的合成呈剂量依赖性增加。Northern印迹分析显示,rCTGF/Hcs24可刺激RGC和RAC细胞中II型胶原蛋白和聚集蛋白聚糖核心蛋白的基因表达,这两种蛋白是软骨细胞成熟的标志物。然而,X型胶原蛋白(肥大软骨细胞的标志物)的基因表达仅在RGC细胞中受到rCTGF/Hcs24的刺激,而在RAC细胞中未受刺激。相反,腱生蛋白-C(关节软骨细胞的标志物)的基因表达在RAC细胞中受到rCTGF/Hcs24的刺激,而在RGC细胞中未受刺激。此外,rCTGF/Hcs24可有效增加RGC细胞的碱性磷酸酶(ALPase)活性和基质钙化,但对RAC细胞无效。这些结果表明,CTGF/Hcs24可促进关节软骨细胞的增殖和分化,但不促进其肥大或钙化。综上所述,数据表明CTGF/Hcs24是关节软骨的直接生长和分化因子,并提示其可能对关节软骨修复有用。