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去极化通过 PI4-激酶机制增加磷脂酰肌醇(PI)4,5-二磷酸水平和 KCNQ 电流。

Depolarization increases phosphatidylinositol (PI) 4,5-bisphosphate level and KCNQ currents through PI 4-kinase mechanisms.

机构信息

Department of Pharmacology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.

Department of Pharmacology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.

出版信息

J Biol Chem. 2010 Mar 26;285(13):9402-9409. doi: 10.1074/jbc.M109.068205. Epub 2010 Jan 27.

Abstract

A growing body of evidence shows that membrane phosphatidylinositol 4,5-bisphosphates (PtdIns(4,5)P(2), PIP(2)) play an important role in cell signaling. The presence of PIP(2) is fundamentally important for maintaining the functions of a large number of ion channels and transporters, and for other cell processes such as vesicle trafficking, mobility, and endo- and exocytosis. PIP(2) levels in the membrane are dynamically modulated, which is an important signaling mechanism for modulation of PIP(2)-dependent cellular processes. In this study, we describe a novel mechanism of membrane PIP(2) modulation. Membrane depolarization induces an elevation in membrane PIP(2), and subsequently increases functions of PIP(2)-sensitive KCNQ potassium channels expressed in Xenopus oocytes. Further evidence suggests that the depolarization-induced elevation of membrane PIP(2) occurs through increased activity of PI4 kinase. With increased recognition of the importance of PIP(2) in cell function, the effect of membrane depolarization in PIP(2) metabolism is destined to have important physiological implications.

摘要

越来越多的证据表明,膜磷脂酰肌醇 4,5-二磷酸(PtdIns(4,5)P(2),PIP(2))在细胞信号转导中发挥重要作用。PIP(2)的存在对于维持大量离子通道和转运体的功能以及其他细胞过程(如囊泡运输、流动性以及内吞作用和胞吐作用)至关重要。膜中 PIP(2)的水平是动态调节的,这是调节 PIP(2)依赖性细胞过程的重要信号机制。在这项研究中,我们描述了一种膜 PIP(2)调节的新机制。膜去极化诱导膜 PIP(2)升高,并随后增加在非洲爪蟾卵母细胞中表达的 PIP(2)敏感的 KCNQ 钾通道的功能。进一步的证据表明,去极化诱导的膜 PIP(2)升高是通过增加 PI4 激酶的活性而发生的。随着对 PIP(2)在细胞功能中的重要性的认识不断提高,膜去极化对 PIP(2)代谢的影响注定具有重要的生理意义。

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