Suppr超能文献

转化生长因子-β1(TGF-β1)对兔关节软骨细胞单层培养物在去分化过程中基质合成的影响。

Effect of transforming growth factor-beta 1 (TGF-beta 1) on matrix synthesis by monolayer cultures of rabbit articular chondrocytes during the dedifferentiation process.

作者信息

Galéra P, Rédini F, Vivien D, Bonaventure J, Penfornis H, Loyau G, Pujol J P

机构信息

Laboratoire de Biochimie du Tissu Conjonctif, CHU Côte de Nacre, Caen, France.

出版信息

Exp Cell Res. 1992 Jun;200(2):379-92. doi: 10.1016/0014-4827(92)90186-c.

Abstract

Since transforming growth factor-beta (TGF-beta) has been shown earlier to induce the chondrocyte phenotype in embryonic rat mesenchymal cells with production of cartilage-specific type II collagen and proteoglycans, it was of interest to determine whether the factor could also influence the differentiation state of articular chondrocytes maintained in monolayer culture. Using rabbit articular chondrocytes (RAC) in primary and passaged cultures, we demonstrate that the loss of the phenotype accompanying the subculture was not significantly influenced by the presence of TGF-beta. The factor exerted an inhibitory effect on collagen synthesis in a 6-day exposure of primary cultures whereas it stimulated that production throughout the subsequent passages. Steady-state levels of mRNAs encoding type I, II, and III procollagens were correlated with the amounts of cognate proteins produced, suggesting that both inhibition and stimulation were exerted at a transcriptional level. The pattern of proteoglycans produced in primary culture, essentially chondroitin sulfate-containing molecules, was altered by the subculture-induced RAC dedifferentiation, as shown by decrease in chondroitin sulfate formation and progressive appearance of hyaluronic acid. Contrasting with its effect on collagen synthesis, TGF-beta did not significantly change the proteoglycan production of RAC in our conditions whenever it was added at the beginning of the primary cultures or in the subsequent passages. Altogether, our data indicate that the effect of TGF-beta on RAC collagen synthesis depends on whether they are fully differentiated. Moreover, the data show that the factor does not prevent the loss of RAC phenotype but rather contributes to the dedifferentiation process since it exerts differential effects on the major components of extracellular matrix, collagen, and proteoglycans.

摘要

由于之前已表明转化生长因子-β(TGF-β)可诱导胚胎大鼠间充质细胞产生软骨特异性II型胶原蛋白和蛋白聚糖,从而呈现软骨细胞表型,因此研究该因子是否也能影响单层培养的关节软骨细胞的分化状态就很有意义。我们使用原代培养和传代培养的兔关节软骨细胞(RAC)进行研究,结果表明,传代培养导致的表型丧失并未因TGF-β的存在而受到显著影响。在原代培养6天的过程中,该因子对胶原蛋白合成具有抑制作用,而在随后的传代过程中则刺激胶原蛋白的产生。编码I型、II型和III型前胶原蛋白的mRNA稳态水平与相应蛋白质的产生量相关,这表明抑制和刺激作用均在转录水平发挥。原代培养中产生的蛋白聚糖模式,主要是含硫酸软骨素的分子,因传代培养诱导的RAC去分化而改变,表现为硫酸软骨素形成减少和透明质酸逐渐出现。与它对胶原蛋白合成的作用相反,无论在原代培养开始时还是在随后的传代过程中添加TGF-β,在我们的实验条件下,它都不会显著改变RAC的蛋白聚糖产生。总之,我们的数据表明,TGF-β对RAC胶原蛋白合成 的影响取决于它们是否已完全分化。此外,数据显示该因子并不能阻止RAC表型的丧失,反而促进了去分化过程,因为它对细胞外基质的主要成分胶原蛋白和蛋白聚糖发挥了不同的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验