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Cell membrane signals in the mechanism of insulin action. Claude P. Brown memorial lecture.

作者信息

Cheng K, Thompson M, Craig J, Schwartz C, Locher E, Larner J

出版信息

Ann Clin Lab Sci. 1984 Jan-Feb;14(1):78-89.

PMID:6320711
Abstract

Present evidence points to the rapid formation of one or several mediators by proteolysis initiated by insulin and, possibly, other hormones. Mediators act intracellularly at a number of subcellular sites, including cytoplasm, mitochondria, endoplasmic reticulum, cell membrane, and nucleus (figure 9). These mediators control enzymes that are controlled by covalent phosphorylation. As a result, the mediators impart an overall integrated control of metabolism. Evidence strongly suggests that the mediators are peptides. They appear to be formed by limited proteolysis from cell membrane proteins or glycoproteins and act as transmembrane signals following the binding of insulin to its receptor and the activation of the insulin-receptor complex.

摘要

相似文献

1
Cell membrane signals in the mechanism of insulin action. Claude P. Brown memorial lecture.
Ann Clin Lab Sci. 1984 Jan-Feb;14(1):78-89.
2
Insulin receptor function and glycogen synthase activity in human skeletal muscle. Physiology and pathophysiology.人类骨骼肌中的胰岛素受体功能与糖原合酶活性。生理学与病理生理学。
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3
[Toward an understanding of the mechanism of action of insulin].[迈向对胰岛素作用机制的理解]
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Jpn J Exp Med. 1984 Oct;54(5):189-93.
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Bioessays. 1994 Oct;16(10):753-9. doi: 10.1002/bies.950161010.

引用本文的文献

1
Further evidence for the involvement of a membrane proteolytic step in insulin action.胰岛素作用中膜蛋白水解步骤参与的进一步证据。
Biochem J. 1985 Apr 1;227(1):137-47. doi: 10.1042/bj2270137.
2
Defective insulin response of cyclic adenosine monophosphate-dependent protein kinase in insulin-resistant humans.胰岛素抵抗人群中依赖环磷酸腺苷的蛋白激酶的胰岛素反应缺陷
J Clin Invest. 1991 Feb;87(2):673-9. doi: 10.1172/JCI115045.