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协同相互作用以及C末端在压力、游离脂肪酸和碱激活TRAAK钾通道中的作用。

Synergistic interaction and the role of C-terminus in the activation of TRAAK K+ channels by pressure, free fatty acids and alkali.

作者信息

Kim Y, Bang H, Gnatenco C, Kim D

机构信息

Department of Physiology and Biophysics, Finch University of Health Sciences, Chicago Medical School, 3333 Green Bay Road, North Chicago, IL 60064, USA.

出版信息

Pflugers Arch. 2001 Apr;442(1):64-72. doi: 10.1007/s004240000496.

Abstract

TRAAK is a member of the tandem-pore K+ channel family, and is expressed mainly in the brain. Using rat TRAAK (rTRAAK), we studied its single-channel kinetics, interactive modes of activation, and the role of the C-terminus on its pressure-, fatty-acid- and pH-sensitivity. When expressed in COS-7 cells, rTRAAK showed a mildly inwardly rectifying single-channel current/voltage relationship in symmetrical 140 mM KCl. Unlike TREK-1 and TREK-2, which are activated by acidic conditions, rTRAAK was activated by alkali conditions, such that a change in intracellular pH from 7.3 to 8.3 and 8.8 increased channel activity 5- and 14-fold, respectively. Pressure and alkali produced a strong synergistic activation, and pressure and arachidonic acid (AA) produced a mild synergistic activation. The only additive effect was observed with alkali and AA. Replacing the C-terminus of rTRAAK with that of TASK-1 or TASK-3 did not affect the response to pressure, AA or alkali. In contrast, replacing the C-terminus of TREK-2 with that of TASK-3 abolished the sensitivity to AA and acid, but not to pressure. These results show that rTRAAK is an alkali-sensing K+ channel that shows synergistic activation with pressure, and that the mechanism of activation of rTRAAK and TREK by free fatty acids are different.

摘要

TRAAK是串联孔道K⁺通道家族的成员,主要在大脑中表达。我们使用大鼠TRAAK(rTRAAK)研究了其单通道动力学、激活的相互作用模式以及C末端对其压力敏感性、脂肪酸敏感性和pH敏感性的作用。当在COS-7细胞中表达时,rTRAAK在对称的140 mM KCl中显示出轻度内向整流的单通道电流/电压关系。与在酸性条件下被激活的TREK-1和TREK-2不同,rTRAAK在碱性条件下被激活,使得细胞内pH从7.3变为8.3和8.8时,通道活性分别增加5倍和14倍。压力和碱产生强烈的协同激活作用,压力和花生四烯酸(AA)产生轻度的协同激活作用。仅在碱和AA之间观察到加和效应。用TASK-1或TASK-3的C末端替换rTRAAK的C末端不影响对压力、AA或碱的反应。相反,用TASK-3的C末端替换TREK-2的C末端消除了对AA和酸的敏感性,但对压力的敏感性未消除。这些结果表明,rTRAAK是一种碱敏感的K⁺通道,与压力表现出协同激活作用,并且游离脂肪酸对rTRAAK和TREK的激活机制不同。

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