首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Constitutive overexpression of c-fos protein in rat liver epithelial cells decreases TGF-β synthesis and increases TGF-β1 receptors
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Constitutive overexpression of c-fos protein in rat liver epithelial cells decreases TGF-β synthesis and increases TGF-β1 receptors

机译:大鼠肝上皮细胞中c-fos蛋白的组成性过表达会降低TGF-β的合成并增加TGF-β1受体

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We have previously shown that rat liver epithelial cells were more sensitive to TGF-β1 when they were transfected with c-fos cDNA. We analyzed the production of TGF-β and TGF-β1 binding proteins in transfected and parental cells. TGF-β-like activity released in the medium was reduced in c-fos expressing cells. TGF-β1 binding sites were more numerous in transfected cells (× 3).Cross-linking studies confirmed that c-fos transfected cells showed increased binding of 125I-TGF-β1 to membrane binding sites corresponding to type I, II and III receptors. Transfected cells internalized and degraded 125I-TGF-β1 more rapidly than parental cells. TGF-β1 incubation rapidly down-regulated the receptors. In parental cells, the down-regulation was total, while in transfected cells, a few binding proteins could still be detected. The c-fos cell line is an interesting tool in analysing the mechanism of action of TGF-β.
机译:先前我们已经表明,当大鼠肝上皮细胞被c-fos cDNA转染时,它们对TGF-β1更为敏感。我们分析了转染和亲代细胞中TGF-β和TGF-β1结合蛋白的产生。在表达c-fos的细胞中,培养基中释放的TGF-β样活性降低。 TGF-β1的结合位点在转染的细胞中更多(×3)。交联研究证实c-fos转染的细胞显示125I-TGF-β1与对应于I,II和III型受体的膜结合位点的结合增加。转染的细胞比亲代细胞更快地内化和降解125I-TGF-β1。 TGF-β1的孵育迅速下调了受体。在亲代细胞中,下调是完全的,而在转染细胞中,仍然可以检测到一些结合蛋白。 c-fos细胞系是分析TGF-β作用机理的有趣工具。

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