Han Min-Su, Kim Jung-Eun, Shin Hong-In, Kim In-San
Cell and Matrix Research Institute, Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Exp Mol Med. 2008 Aug 31;40(4):453-60. doi: 10.3858/emm.2008.40.4.453.
betaig-h3 is a TGF-beta-induced extracellular matrix protein which is expressed in many tissues including bones and cartilages. In previous reports, we showed that betaig-h3 mediates cell adhesion and migration and, especially in bones, negatively regulates the mineralization in the end stage of endochondral ossification. Here, to elucidate the expression pattern and role of betaig-h3 in chondrocyte differentiation, ATDC5 chondrocytes and embryonic and postnatal mice were used for in vitro differentiation studies and in vivo studies, respectively. betaig-h3 was strongly induced by the treatment of TGF-beta1 and the expression level of betaig-h3 mRNA and protein were highly expressed in the early stages of differentiation but decreased in the late stages in ATDC5. Furthermore, the patterns of TGF-beta1, -beta2, and -beta3 mRNA expression were concurrent with betaig-h3 in ATDC5. betaig-h3 was deeply stained in perichondrium (PC), periosteum (PO), and prehypertrophic chondrocytes (PH) through the entire period of endochondral ossification in mice. betaig-h3 was mainly expressed in PC and PH at embryonic days and obviously in PH in postnatal days. These results suggest that betaig-h3 may play a critical role as a regulator of chondrogenic differentiation in endochondral ossification.
βig-h3是一种由转化生长因子-β(TGF-β)诱导的细胞外基质蛋白,在包括骨骼和软骨在内的许多组织中均有表达。在先前的报道中,我们发现βig-h3介导细胞黏附和迁移,尤其是在骨骼中,它在软骨内骨化末期对矿化起负向调节作用。在此,为了阐明βig-h3在软骨细胞分化中的表达模式和作用,分别使用ATDC5软骨细胞以及胚胎期和出生后的小鼠进行体外分化研究和体内研究。用TGF-β1处理可强烈诱导βig-h3表达,在ATDC5细胞分化早期,βig-h3 mRNA和蛋白的表达水平较高,但在晚期降低。此外,在ATDC5细胞中,TGF-β1、-β2和-β3 mRNA的表达模式与βig-h3一致。在小鼠软骨内骨化的整个过程中,βig-h3在软骨膜(PC)、骨膜(PO)和前肥大软骨细胞(PH)中均有深染。在胚胎期,βig-h3主要在PC和PH中表达,在出生后则明显在PH中表达。这些结果表明,βig-h3可能作为软骨内骨化过程中软骨形成分化的调节因子发挥关键作用。