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磷脂酰肌醇 4,5-二磷酸对 hEAG1 通道的双重调节。

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

机构信息

Departamento de Fisiología y Biofísica, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, San Luis Potosí, SLP 78210, Mexico.

Facultad de Ingeniería, Universidad Autónoma de Baja California, Mexicali, BC, 21280, Mexico.

出版信息

Biochem Biophys Res Commun. 2018 Sep 18;503(4):2531-2535. doi: 10.1016/j.bbrc.2018.07.011. Epub 2018 Jul 4.

Abstract

The ether-à-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 (PIP) by using different strategies to manipulate the levels of this lipid, and the patch clamp technique. We found that depletion of endogenous PIP 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 PIP to increase the level of this lipid on the plasma membrane, also induced an inhibition of hEAG1. In summary, our results indicate that PIP have dual effects on hEAG1 channels and its action as activator or inhibitor depends on its initial level on the plasma membrane.

摘要

醚-α--go-go1 (EAG1, Kv10.1) K 通道是电压门控 K 通道家族的成员,主要在中枢神经系统和癌细胞中表达。膜脂调节几种电压门控 K 通道,但它们对 EAG1 通道的影响尚未得到充分探索。在这里,我们通过使用不同的策略来操纵这种脂质的水平,并使用膜片钳技术,研究了磷脂酰肌醇 4,5-二磷酸 (PIP) 对 hEAG1 通道的调节。我们发现,通过激活斑马鱼的电压感应磷酸酶 (Dr-VSP) 或人毒蕈碱型 1 受体 (hM1R) 激活内源性 PIP,会抑制 hEAG1 电流;然而,应用外源性 PIP 增加质膜上这种脂质的水平,也会诱导 hEAG1 的抑制。总之,我们的结果表明,PIP 对 hEAG1 通道有双重作用,其作为激活剂或抑制剂的作用取决于其在质膜上的初始水平。

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