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环核苷酸和其他细胞内介质调节分泌的机制。

Mechanisms by which cyclic nucleotides and other intracellular mediators regulate secretion.

作者信息

de Jonge H R, Lohmann S M

出版信息

Ciba Found Symp. 1985;112:116-38. doi: 10.1002/9780470720936.ch7.

Abstract

The regulation of Na+ and Cl- transport across surface membranes and tight junctions of intestinal epithelium is mediated through at least three intracellular messengers: (i) 3',5'-cyclic AMP, activating two types of cyclic AMP-dependent protein kinase, (ii) 3',5'-cyclic GMP, binding to a unique isoenzyme of cyclic GMP-dependent protein kinase, enriched in the intestinal brush border, and (iii) Ca2+ ions, partially acting through calmodulin and a Ca2+/phospholipid-dependent protein kinase (C kinase). Recent data on the subcellular distribution and molecular properties of the high affinity cyclic nucleotide and Ca2+ receptors, their influence on the phosphorylation state of specific membrane proteins, and the possible role of these target proteins in ion transport regulation, are reviewed. The following aspects are accentuated: (1) the asymmetrical compartmentation of cyclic AMP-dependent protein kinase isoenzymes in the enterocyte and its functional implications; (2) the structure and function of microvillous cyclic GMP-dependent protein kinase; (3) the integration of cyclic AMP and cyclic GMP signals through co-phosphorylation of a 25 000 Mr protein in the intestinal-microvilli; (4) the identification of C kinase in villous and crypt cells; (5) various levels of interaction between cyclic nucleotide and Ca2+ signals; and (6) priority areas for future studies on stimulus-secretion coupling.

摘要

钠和氯跨肠上皮表面膜及紧密连接的转运调节至少由三种细胞内信使介导

(i)3',5'-环磷酸腺苷(cAMP),激活两种类型的cAMP依赖性蛋白激酶;(ii)3',5'-环磷酸鸟苷(cGMP),与一种独特的cGMP依赖性蛋白激酶同工酶结合,该同工酶在肠刷状缘富集;(iii)钙离子,部分通过钙调蛋白和一种Ca2+/磷脂依赖性蛋白激酶(C激酶)起作用。本文综述了关于高亲和力环核苷酸和钙离子受体的亚细胞分布及分子特性、它们对特定膜蛋白磷酸化状态的影响以及这些靶蛋白在离子转运调节中可能作用的最新数据。重点强调了以下几个方面:(1)肠细胞中cAMP依赖性蛋白激酶同工酶的不对称区室化及其功能意义;(2)微绒毛cGMP依赖性蛋白激酶的结构与功能;(3)通过肠微绒毛中一种25000道尔顿蛋白的共磷酸化整合cAMP和cGMP信号;(4)绒毛和隐窝细胞中C激酶的鉴定;(5)环核苷酸和钙离子信号之间的不同层次相互作用;(6)刺激-分泌偶联未来研究的重点领域。

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