Dual regulation of hEAG1 channels by phosphatidylinositol 4,5-bisphosphate

被引:6
|
作者
Delgado-Ramirez, Mayra [1 ]
Lopez-Izquierdo, Angelica [2 ]
Rodriguez-Menchaca, Aldo A. [1 ]
机构
[1] Univ Autonoma San Luis Potosi, Fac Med, Dept Fisiol & Biofis, Venustiano Carranza 2405, San Luis Potosi 78210, SLP, Mexico
[2] Univ Autonoma Baja California, Fac Ingn, Mexicali 21280, Baja California, Mexico
关键词
Potassium channels; Lipids; Ion channel regulation; Patch clamp; POTASSIUM CHANNELS; K+ CHANNELS; ACTIVATION; PIP2; INHIBITION; FAMILY;
D O I
10.1016/j.bbrc.2018.07.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ether-a-go-go1 (EAG1, Kv10.1) K+ channel is a member of the voltage-gated K+ channel family mainly expressed in the central nervous system and cancer cells. Membrane lipids regulate several voltage-gated K+ channels but their influence on EAG1 channels has been poorly explored. Here we have studied the regulation of hEAG1 channels by phosphatidylinositol 4,5-bisfofate (PIP2) by using different strategies to manipulate the levels of this lipid, and the patch clamp technique. We found that depletion of endogenous PIP2 by activation of the voltage-sensing phosphatase from Danio rerio (Dr-VSP) or the human muscarinic type-1 receptor (hM1R) inhibits hEAG1 currents; however, the application of exogenous PIP2 to increase the level of this lipid on the plasma membrane, also induced an inhibition of hEAG1. In summary, our results indicate that PIP2 have dual effects on hEAG1 channels and its action as activator or inhibitor depends on its initial level on the plasma membrane. (C) 2018 Elsevier Inc. All rights reserved.
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页码:2531 / 2535
页数:5
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