Inoue H, Kondo J, Koike T, Shukunami C, Hiraki Y
Department of Biochemistry, Osaka University Faculty of Dentistry, Japan.
Biochem Biophys Res Commun. 1997 Dec 18;241(2):395-400. doi: 10.1006/bbrc.1997.7820.
Chondrocytes are unique among non-transformed cells in that they are capable of anchorage-independent growth in soft agar. Fibroblast growth factor (FGF) is known as a potent colony-stimulating factor for chondrocytes. However, cartilage extracts contain a potent colony-stimulating activity which is not explicable only by contaminating FGF. We previously isolated the 25 kDa cartilage-specific glycoprotein chondromodulin-I (ChM-I) which stimulates the growth of chondrocytes. In the present study, we observed that ChM-I stimulates the colony formation of rabbit growth plate chondrocytes in agarose culture. ChM-I alone weakly stimulated the formation of chondrocyte colonies, but it markedly stimulated colony formation synergistically in the presence of an optimal dose of FGF-2. This effect was dependent on the dose of ChM-I. These results suggest that ChM-I participates in an autocrine signaling mechanism for the anchorage-independent growth of chondrocytes in vitro.
软骨细胞在未转化细胞中独具特性,因为它们能够在软琼脂中进行不依赖贴壁的生长。成纤维细胞生长因子(FGF)是已知的对软骨细胞有强大集落刺激作用的因子。然而,软骨提取物含有一种强大的集落刺激活性,这仅用污染的FGF无法解释。我们之前分离出了25 kDa的软骨特异性糖蛋白软骨调节素-I(ChM-I),它能刺激软骨细胞生长。在本研究中,我们观察到ChM-I在琼脂糖培养中刺激兔生长板软骨细胞的集落形成。单独的ChM-I对软骨细胞集落形成的刺激作用较弱,但在最佳剂量的FGF-2存在时,它能显著协同刺激集落形成。这种效应依赖于ChM-I的剂量。这些结果表明,ChM-I参与了体外软骨细胞不依赖贴壁生长的自分泌信号机制。