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首页> 外文期刊>Molecular cell >Exocytosis of Insulin Promotes Insulin Gene Transcription via the Insulin Receptor/PI-3 Kinase/p70 s6 Kinase and CaM Kinase Pathways
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Exocytosis of Insulin Promotes Insulin Gene Transcription via the Insulin Receptor/PI-3 Kinase/p70 s6 Kinase and CaM Kinase Pathways

机译:胰岛素的胞吐作用通过胰岛素受体/ PI-3激酶/ p70 s6激酶和CaM激酶途径促进胰岛素基因转录

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摘要

The control of glucose homeostasis by insulin requires, in addition to the glucose-induced insulin release, a highly dynamic control of insulin biosynthesis. Although elevated glucose concentrations have been shown to trigger insulin biosynthesis at the levels of transcription and translation, the molecular mechanisms underlying the immediate transcriptional control are poorly understood. By investigating signal transduction pathways involved in the "glucose-dependent" transcriptional control, thereby analyzing endogenous (prepro)insulin mRNA levels and monitoring on-line insulin promoter-driven GFP expression, we provide, for the first time, evidence that physiologically stimulated insulin secretion from the pancreatic β cell promotes insulin biosynthesis by enhancing insulin gene transcription in an autocrine manner. We show that secreted insulin acts via β-cell insulin receptors and up-regulates insulin gene transcription by signaling through the IRS-2/PI-3 kinase/p70 s6k and CaM kinase pathways.
机译:通过胰岛素控制葡萄糖稳态,除了葡萄糖诱导的胰岛素释放外,还需要高度动态地控制胰岛素的生物合成。尽管已经表明升高的葡萄糖浓度在转录和翻译水平上触发了胰岛素的生物合成,但是对即时转录控制的分子机制知之甚少。通过研究参与“葡萄糖依赖性”转录控制的信号转导途径,从而分析内源性(前原胰岛素)mRNA水平并监测在线胰岛素启动子驱动的GFP表达,我们首次提供了生理刺激胰岛素的证据胰腺β细胞的分泌通过以自分泌方式增强胰岛素基因的转录来促进胰岛素的生物合成。我们显示,分泌的胰岛素通过β细胞胰岛素受体起作用,并通过IRS-2 / PI-3激酶/ p70 s6k和CaM激酶途径进行信号传导,从而上调胰岛素基因的转录。

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