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src癌基因转化的细胞中表皮生长因子受体的下调。

Down-modulation of EGF receptors in cells transformed by the src oncogene.

作者信息

Wasilenko W J, Shawver L K, Weber M J

出版信息

J Cell Physiol. 1987 Jun;131(3):450-7. doi: 10.1002/jcp.1041310318.

Abstract

The effects of src oncogene expression on epidermal growth factor (EGF) receptors have been investigated in mouse 3T3 and rat-1 fibroblasts. Transformation of both cell types with src resulted in marked reductions in cellular EGF receptor levels, as assayed by either 125I-EGF binding or immunoprecipitation of receptor protein from radiolabeled cell lysates. In contrast to cells transformed by other types of retroviral oncogenes, the loss of EGF receptors in the src-transformed cells did not appear to be due to secreted transforming growth factor-alpha (TGF-alpha), since such factors were undetectable in culture fluids from the src-transformed cells. By several criteria of transformation, an EGF-receptorless cell line infected with src was shown to be transformed, suggesting that EGF receptors themselves are not obligatory to the src transformation process. We suggest that pp60src down-modulates EGF receptors by an intracellular mechanism and that the loss of the receptors is symptomatic of more general effects of pp60src on the machinery of growth regulation.

摘要

src癌基因表达对表皮生长因子(EGF)受体的影响已在小鼠3T3和大鼠-1成纤维细胞中进行了研究。用src对这两种细胞类型进行转化,导致细胞EGF受体水平显著降低,这是通过125I-EGF结合或从放射性标记的细胞裂解物中免疫沉淀受体蛋白来测定的。与由其他类型逆转录病毒癌基因转化的细胞不同,src转化细胞中EGF受体的丧失似乎不是由于分泌的转化生长因子-α(TGF-α),因为在src转化细胞的培养液中检测不到此类因子。根据几种转化标准,感染src的无EGF受体细胞系被证明发生了转化,这表明EGF受体本身对于src转化过程并非必不可少。我们认为pp60src通过细胞内机制下调EGF受体,并且受体的丧失是pp60src对生长调节机制更广泛影响的症状表现。

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