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在软骨前凝聚物形成过程中,转化生长因子β1、β2、β3和β5可刺激N-钙黏蛋白、神经细胞黏附分子、纤连蛋白和腱生蛋白的表达。

Expression of N-cadherin, N-CAM, fibronectin and tenascin is stimulated by TGF-beta1, beta2, beta3 and beta5 during the formation of precartilage condensations.

作者信息

Chimal-Monroy J, Díaz de León L

机构信息

Department of Cell Biology, Instituto de Investigaciones Biomédicas, UNAM, México D.F., México.

出版信息

Int J Dev Biol. 1999 Jan;43(1):59-67.

Abstract

Cell surface adhesion and extracellular matrix proteins are known to play a key role in the formation of cell condensations during skeletal development, and their formation is crucial for the expression of cartilage-specific genes. However, little is known about the relationship between adhesion molecules (N-cadherin and N-CAM), extracellular matrix proteins (fibronectin and tenascin) and TGF-beta1, TGF-beta2 and TGF-beta3 during in vitro precartilage condensations in mouse chondrogenesis. On these bases, we determined the participation of mammalian TGF-beta1, TGF-beta2 and TFG-beta3 and Xenopus TGF-beta5 on the expression of cell surface adhesion and extracellular matrix proteins during the formation of precartilage condensations. Also, we characterized the effects of TGF-betas on proteoglycan metabolism at different cellular densities in mouse embryonic limb bud mesenchymal cells. In TGF-beta1 and TGF-beta5-treated cultures, proteoglycan biosynthesis was higher than in controls, while there were no differences in proteoglycan catabolism, which caused the accumulation of cartilage extracellular matrix. When mesenchymal cells were seeded at three different cellular densities in the presence of TGF-betas, only high density cultures presented increased stimulation of proteoglycan biosynthesis, compared to low and intermediate densities. To determine whether the effect of TGF-betas on precartilage condensations is mediated through the expression of N-cadherin, N-CAM, fibronectin and tenascin, we evaluated their expression. Results showed that TGF-beta1, TGF-beta2, TGF-beta3, and TGF-beta5 differentially enhanced the expression of N-cadherin, N-CAM, fibronectin and tenascin in precartilage condensations, suggesting that TGF-beta isoforms play an important role in the establishment of cell-cell and cell-extracellular matrix interactions during precartilage condensations.

摘要

已知细胞表面黏附蛋白和细胞外基质蛋白在骨骼发育过程中细胞凝聚的形成中起关键作用,并且它们的形成对于软骨特异性基因的表达至关重要。然而,在小鼠软骨形成过程中的体外软骨前凝聚期间,关于黏附分子(N-钙黏蛋白和N-细胞黏附分子)、细胞外基质蛋白(纤连蛋白和腱生蛋白)与转化生长因子-β1、转化生长因子-β2和转化生长因子-β3之间的关系,人们了解甚少。基于这些情况,我们确定了哺乳动物转化生长因子-β1、转化生长因子-β2、转化生长因子-β3和非洲爪蟾转化生长因子-β5在软骨前凝聚形成过程中对细胞表面黏附蛋白和细胞外基质蛋白表达的参与情况。此外,我们还表征了转化生长因子-β在小鼠胚胎肢芽间充质细胞不同细胞密度下对蛋白聚糖代谢的影响。在转化生长因子-β1和转化生长因子-β5处理的培养物中,蛋白聚糖生物合成高于对照组,而蛋白聚糖分解代谢没有差异,这导致了软骨细胞外基质的积累。当间充质细胞在存在转化生长因子-β的情况下以三种不同细胞密度接种时,与低密度和中等密度相比,只有高密度培养物中蛋白聚糖生物合成的刺激增加。为了确定转化生长因子-β对软骨前凝聚的作用是否通过N-钙黏蛋白、N-细胞黏附分子、纤连蛋白和腱生蛋白的表达介导,我们评估了它们的表达。结果表明,转化生长因子-β1、转化生长因子-β2、转化生长因子-β3和转化生长因子-β5在软骨前凝聚中差异增强了N-钙黏蛋白、N-细胞黏附分子、纤连蛋白和腱生蛋白的表达,这表明转化生长因子-β亚型在软骨前凝聚期间细胞-细胞和细胞-细胞外基质相互作用的建立中起重要作用。

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