Niikura Takahiro, Reddi A Hari
University of California, Davis School of Medicine, Sacramento, CA 95817, USA.
Arthritis Rheum. 2007 Jul;56(7):2312-21. doi: 10.1002/art.22659.
To investigate the role of transforming growth factor beta (TGFbeta)/bone morphogenetic protein (BMP) superfamily members on accumulation of superficial zone protein (SZP) in articular chondrocytes and synoviocytes.
Chondrocytes and synoviocytes were isolated from articular cartilage and synovium from calf stifle joints and cultured as monolayers in serum-free chemically defined medium. Articular chondrocytes were isolated from 3 distinct zones of the cartilage: superficial, middle, and deep. Accumulation of SZP in the culture medium in response to various members of the TGFbeta/BMP superfamily was demonstrated by immunoblotting and quantified by enzyme-linked immunosorbent assay.
TGFbeta stimulated SZP accumulation in both superficial zone chondrocytes and synoviocytes. The 3 isoforms of TGFbeta elicited a similar dose response. Inhibition of TGFbeta receptor type I kinase by the specific inhibitor SB431542 abolished the TGFbeta-stimulated accumulation of SZP. BMPs up-regulated SZP accumulation in the superficial zone; however, the magnitude of the effects was not as great as was observed with TGFbeta. There was an additive action between TGFbeta and BMP on SZP accumulation. The response of synoviocytes to BMP was stronger than that of superficial zone chondrocytes. Activin up-regulated SZP accumulation in synoviocytes, but not in chondrocytes.
TGFbeta is a critical regulator of SZP accumulation in both superficial zone articular chondrocytes and synoviocytes. TGFbeta and BMP have an additive effect. Synoviocytes are more sensitive to BMP family members and activins than are superficial zone articular chondrocytes. Thus, regulation of SZP accumulation by TGFbeta /BMP superfamily members is regulated differently in articular chondrocytes and synoviocytes.
研究转化生长因子β(TGFβ)/骨形态发生蛋白(BMP)超家族成员在关节软骨细胞和滑膜细胞中浅表区蛋白(SZP)积累过程中的作用。
从犊牛膝关节的关节软骨和滑膜中分离软骨细胞和滑膜细胞,并在无血清化学限定培养基中单层培养。关节软骨细胞从软骨的3个不同区域分离:浅表区、中间区和深层区。通过免疫印迹法证实培养基中SZP在TGFβ/BMP超家族各成员作用下的积累,并通过酶联免疫吸附测定法进行定量。
TGFβ刺激浅表区软骨细胞和滑膜细胞中SZP的积累。TGFβ的3种同工型引发相似的剂量反应。特异性抑制剂SB431542对I型TGFβ受体激酶的抑制作用消除了TGFβ刺激的SZP积累。BMP上调浅表区SZP的积累;然而,其作用程度不如TGFβ显著。TGFβ和BMP在SZP积累上具有相加作用。滑膜细胞对BMP的反应强于浅表区软骨细胞。激活素上调滑膜细胞中SZP的积累,但在软骨细胞中无此作用。
TGFβ是浅表区关节软骨细胞和滑膜细胞中SZP积累的关键调节因子。TGFβ和BMP具有相加作用。滑膜细胞比浅表区关节软骨细胞对BMP家族成员和激活素更敏感。因此,TGFβ/BMP超家族成员对SZP积累的调节在关节软骨细胞和滑膜细胞中存在差异。