Istituto Nazionale per la Ricerca sul Cancro, viale Benedetto XV, 10, 16132, Genova, Italy.
Cytotechnology. 1991 Feb;5(Suppl 1):41-4. doi: 10.1007/BF00736804.
The establishment of a cell culture system promoting chondrocyte differentiation has been utilized to better characterize phenotypic stages of chondrogenesis at the cellular level. Although the expression of the type II collagen gene has been studied during "in vitro" chondrocyte differentiation, little is known about the expression of the gene coding for its receptor: anchorin CII. The modulation of the anchorin mRNA steady state level in chick embryo chondrocytes at different developmental stages is described here.The anchorin mRNA level was low in dedifferentiated chondrocytes, progressively increased after the cell transfer into suspension (a condition promoting differentiation), reached its maximal value after 4 weeks and decreased after 5 weeks.Therefore anchorin CII mRNA reaches its maximum level in hypertrophic stage II chondrocytes.
建立促进软骨细胞分化的细胞培养系统,有助于更好地在细胞水平上描述软骨生成的表型阶段。尽管已经研究了在“体外”软骨细胞分化过程中 II 型胶原基因的表达,但对于编码其受体锚蛋白 CII 的基因的表达知之甚少。本文描述了在不同发育阶段的鸡胚软骨细胞中锚蛋白 mRNA 稳定水平的变化。在去分化的软骨细胞中,锚蛋白 mRNA 水平较低,在细胞转移到悬浮状态后(促进分化的条件)逐渐增加,在 4 周后达到最大值,5 周后降低。因此,锚蛋白 CII mRNA 在肥大期 II 型软骨细胞中达到最大值。