Katagiri Yohko U, Yamagata Tatsuya
Laboratory of Developmental Biology, Mitsubishi-Kasei Institute of Life Sciences, 11 Minamiooya, Machida-shi, Tokyo 194, JAPAN.
Dev Growth Differ. 1981;23(4):335-348. doi: 10.1111/j.1440-169X.1981.00335.x.
The effect of chick embryo extract on the phenotypic expression of differentiated chondrocytes has been studied in consideration of the fact that these cells are well characterized by certain specific cell products, such as type H proteochondroitin sulfate and type II collagen. In this study, we utilized floating chondrocytes derived from chick embryonic sterna, which can be cultured in suspension with no apparent change in the type of cell products for at least a period of eight weeks, as described in a previous paper (1). In the presence of chick embryo extract in the medium, the floating chondrocytes became attached to the bottom of the culture dish, and the attached cells took on a fibroblast-like appearance. Biochemical analyses of the proteochondroitin sulfate and collagen synthesized by the attached cells revealed that if the culture medium was renewed everyday, the cells having a fibroblast-like appearance continued to synthesize type H proteochondroitin sulfate and type II collagen. When however, the medium was replaced every other day, the synthesis of both proteochondroitin sulfate and collagen by the attached cells switched from the chondrocyte type to the fibroblast type, i.e. the synthesis of type M proteochondroitin sulfate and type I collagen, with little change in the fibroblast-like appearance. The results show that the morphological features of chondrocytes are not necessarily associated with the biochemical properties of these cells, and further suggest that, in chick embryo extract, there is no modulator capable of acting directly on the chondrocytes to bring about phenotypic changes with respect to the synthesis of collagen and proteoglycans.
鉴于分化的软骨细胞具有某些特定的细胞产物,如硫酸H型蛋白聚糖和II型胶原蛋白,因而对鸡胚提取物对这些细胞表型表达的影响进行了研究。在本研究中,我们利用了源自鸡胚胸骨的悬浮软骨细胞,正如之前一篇论文(1)中所述,这些细胞可以在悬浮状态下培养至少八周,细胞产物类型无明显变化。在培养基中存在鸡胚提取物的情况下,悬浮软骨细胞会附着于培养皿底部,附着的细胞呈现出成纤维细胞样外观。对附着细胞合成的硫酸蛋白聚糖和胶原蛋白进行生化分析发现,如果每天更换培养基,具有成纤维细胞样外观的细胞会继续合成硫酸H型蛋白聚糖和II型胶原蛋白。然而,当隔天更换培养基时,附着细胞合成的硫酸蛋白聚糖和胶原蛋白均从软骨细胞类型转变为成纤维细胞类型,即合成M型硫酸蛋白聚糖和I型胶原蛋白,而成纤维细胞样外观变化不大。结果表明,软骨细胞的形态特征不一定与这些细胞的生化特性相关,进一步表明,在鸡胚提取物中,不存在能够直接作用于软骨细胞以引起胶原蛋白和蛋白聚糖合成方面表型变化的调节剂。