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转化生长因子-β1可防止骨骺软骨细胞肥大:对软骨基质蛋白和金属蛋白酶基因表达的调控

TGF-beta 1 prevents hypertrophy of epiphyseal chondrocytes: regulation of gene expression for cartilage matrix proteins and metalloproteases.

作者信息

Ballock R T, Heydemann A, Wakefield L M, Flanders K C, Roberts A B, Sporn M B

机构信息

Laboratory of Chemoprevention, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Dev Biol. 1993 Aug;158(2):414-29. doi: 10.1006/dbio.1993.1200.

Abstract

Using an in vitro model of rat epiphyseal chondrocyte differentiation in which cells are maintained in a three-dimensional cell pellet, we show that exogenous TGF-beta 1 reversibly prevents terminal differentiation of epiphyseal chondrocytes into hypertrophic cells. Through maintenance of gene expression for the cartilage matrix proteins type II collagen and aggrecan core protein, and with coordinate inhibition of expression of genes encoding the metalloproteases collagenase and stromelysin, TGF-beta 1 stabilizes the phenotype of the prehypertrophic epiphyseal chondrocyte. This ability of TGF-beta 1 to stabilize the cartilage phenotype is critically dependent on culture conditions. Epiphyseal chondrocytes cultured as a subconfluent monolayer of cells dedifferentiate (reduce type II collagen and aggrecan core protein expression, increase metalloprotease expression, and acquire a spindled morphology) in response to short-term TGF-beta 1 treatment. Increasing the initial seeding density and allowing the cells to become multilayered prior to the addition of growth factor reverse the effects of TGF-beta 1 on type II collagen and transin/stromelysin gene expression and maintain a rounded cellular morphology. This finding emphasizes the importance of considering cell density and environmental context in the analysis of the regulatory action of peptide growth factors in general and of the TGF-beta s in particular. We propose that one function of TGF-beta 1 during endochondral ossification is regulation of chondrocyte growth and differentiation through modulation of the relative expression of cartilage matrix proteins and metalloproteases. This function of TGF-beta 1 helps illustrate how the regulation of diverse cellular processes such as matrix synthesis, matrix degradation, and cell growth and differentiation may be coordinated at the molecular level by a single peptide growth factor.

摘要

利用大鼠骨骺软骨细胞分化的体外模型(细胞在三维细胞球中培养),我们发现外源性转化生长因子β1(TGF-β1)可可逆地阻止骨骺软骨细胞终末分化为肥大细胞。通过维持软骨基质蛋白II型胶原蛋白和聚集蛋白聚糖核心蛋白的基因表达,并协同抑制编码金属蛋白酶胶原酶和基质溶解素的基因表达,TGF-β1稳定了肥大前期骨骺软骨细胞的表型。TGF-β1稳定软骨表型的这种能力严重依赖于培养条件。作为亚汇合单层细胞培养的骨骺软骨细胞在短期TGF-β1处理下会去分化(降低II型胶原蛋白和聚集蛋白聚糖核心蛋白的表达,增加金属蛋白酶的表达,并获得纺锤状形态)。增加初始接种密度并在添加生长因子之前使细胞形成多层可逆转TGF-β1对II型胶原蛋白和转胶酶/基质溶解素基因表达的影响,并维持圆形细胞形态。这一发现强调了在分析肽生长因子尤其是TGF-βs的调节作用时考虑细胞密度和环境背景的重要性。我们提出,在软骨内骨化过程中,TGF-β1的一个功能是通过调节软骨基质蛋白和金属蛋白酶的相对表达来调控软骨细胞的生长和分化。TGF-β1的这一功能有助于说明单一肽生长因子如何在分子水平上协调多种细胞过程的调节,如基质合成、基质降解以及细胞生长和分化。

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