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Insulin receptor substrate 1 is required for insulin-mediated mitogenic signal transduction.

机译:胰岛素介导的有丝分裂信号转导需要胰岛素受体底物1。

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摘要

Insulin treatment of mammalian cells immediately stimulates the tyrosine phosphorylation of a cellular protein of 185 kDa referred to as pp185 or IRS-1 (insulin receptor substrate 1). The potential role of the IRS-1 protein in insulin signaling has been examined by microinjecting affinity-purified antibodies into living cells. Stably transfected Rat-1 fibroblasts, which overexpress the human insulin receptor, were microinjected and subsequently stimulated with insulin or other growth factors. Progression through the cell cycle was monitored by using a single-cell assay, which employs bromodeoxyuridine labeling of DNA and analysis with immunofluorescence microscopy. Microinjection of anti-IRS-1 antibody completely inhibited incorporation of bromodeoxyuridine into the nuclei of cells stimulated with insulin or insulin-like growth factor I but did not affect cells stimulated with serum or a variety of purified growth factors. These studies indicate that IRS-1 is a critical component of the insulin and insulin-like growth factor I signaling pathways, which lead to DNA synthesis and cell growth.
机译:哺乳动物细胞的胰岛素处理立即刺激了称为pp185或IRS-1(胰岛素受体底物1)的185 kDa细胞蛋白的酪氨酸磷酸化。通过将亲和纯化的抗体显微注射到活细胞中,已经检查了IRS-1蛋白在胰岛素信号传导中的潜在作用。显微注射过表达人胰岛素受体的稳定转染的Rat-1成纤维细胞,然后用胰岛素或其他生长因子刺激。通过使用单细胞测定法监测整个细胞周期的进程,该方法采用溴脱氧尿苷标记DNA,并用免疫荧光显微镜分析。显微注射抗IRS-1抗体可完全抑制溴脱氧尿苷掺入胰岛素或胰岛素样生长因子I刺激的细胞核中,但不影响血清或多种纯化的生长因子刺激的细胞。这些研究表明,IRS-1是胰岛素和类胰岛素生长因子I信号通路的关键组成部分,可导致DNA合成和细胞生长。

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