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从串扰到协同作用:胆固醇和 PI(4,5)P 对内向整流钾通道的综合影响。

From Crosstalk to Synergism: The Combined Effect of Cholesterol and PI(4,5)P on Inwardly Rectifying Potassium Channels.

机构信息

Department of Pharmacology, Addiction Science and Toxicology, College of Medicine, The University of Tennessee Health Science Center, Memphis, TN, USA.

Department of Chemistry, University of Illinois Chicago, Chicago, IL, USA.

出版信息

Adv Exp Med Biol. 2023;1422:169-191. doi: 10.1007/978-3-031-21547-6_6.

DOI:10.1007/978-3-031-21547-6_6
PMID:36988881
Abstract

Inwardly rectifying potassium (Kir) channels are integral membrane proteins that control the flux of potassium ions across cell membranes and regulate membrane permeability. All eukaryotic Kir channels require the membrane phospholipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P) for activation. In recent years, it has become evident that the function of many members of this family of channels is also mediated by another essential lipid-cholesterol. Here, we focus on members of the Kir2 and Kir3 subfamilies and their modulation by these two key lipids. We discuss how PI(4,5)P and cholesterol bind to Kir2 and Kir3 channels and how they affect channel activity. We also discuss the accumulating evidence indicating that there is interplay between PI(4,5)P and cholesterol in the modulation of Kir2 and Kir3 channels. In particular, we review the crosstalk between PI(4,5)P and cholesterol in the modulation of the ubiquitously expressed Kir2.1 channel and the synergy between these two lipids in the modulation of the Kir3.4 channel, which is primarily expressed in the heart. Additionally, we demonstrate that there is also synergy in the modulation of Kir3.2 channels, which are expressed in the brain. These observations suggest that alterations in the relative levels PI(4,5)P and cholesterol may fine-tune Kir channel activity.

摘要

内向整流钾 (Kir) 通道是整合膜蛋白,控制钾离子跨细胞膜的流动并调节膜通透性。所有真核 Kir 通道的激活都需要膜磷脂磷脂酰肌醇 4,5-二磷酸 (PI(4,5)P)。近年来,人们已经清楚地认识到,该家族许多成员的功能也受到另一种必需脂质-胆固醇的调节。在这里,我们重点关注 Kir2 和 Kir3 亚家族的成员及其与这两种关键脂质的调节。我们讨论了 PI(4,5)P 和胆固醇如何与 Kir2 和 Kir3 通道结合以及它们如何影响通道活性。我们还讨论了越来越多的证据表明,PI(4,5)P 和胆固醇在调节 Kir2 和 Kir3 通道方面存在相互作用。特别是,我们回顾了 PI(4,5)P 和胆固醇在调节普遍表达的 Kir2.1 通道中的相互作用以及这两种脂质在调节主要在心脏表达的 Kir3.4 通道中的协同作用。此外,我们证明 Kir3.2 通道的调节也存在协同作用,Kir3.2 通道在大脑中表达。这些观察结果表明,PI(4,5)P 和胆固醇的相对水平的改变可能会微调 Kir 通道的活性。

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本文引用的文献

1
A molecular switch controls the impact of cholesterol on a Kir channel.一种分子开关控制胆固醇对 Kir 通道的影响。
Proc Natl Acad Sci U S A. 2022 Mar 29;119(13):e2109431119. doi: 10.1073/pnas.2109431119. Epub 2022 Mar 25.
2
Structural insights into GIRK2 channel modulation by cholesterol and PIP.胆固醇和 PIP 对 GIRK2 通道调节的结构见解
Cell Rep. 2021 Aug 24;36(8):109619. doi: 10.1016/j.celrep.2021.109619.
3
Cryo-EM analysis of PIP regulation in mammalian GIRK channels.冷冻电镜分析哺乳动物 GIRK 通道中 PIP 的调节作用。
Elife. 2020 Aug 26;9:e60552. doi: 10.7554/eLife.60552.
4
Atomistic basis of opening and conduction in mammalian inward rectifier potassium (Kir2.2) channels.在哺乳动物内向整流钾 (Kir2.2) 通道中打开和传导的原子基础。
J Gen Physiol. 2020 Jan 6;152(1). doi: 10.1085/jgp.201912422.
5
On the mechanism of GIRK2 channel gating by phosphatidylinositol bisphosphate, sodium, and the Gβγ dimer.GIRK2 通道门控的机制:由双磷脂酰肌醇、钠离子和 Gβγ 二聚体调控。
J Biol Chem. 2019 Dec 6;294(49):18934-18948. doi: 10.1074/jbc.RA119.010047. Epub 2019 Oct 28.
6
Cholesterol Binding Sites in Inwardly Rectifying Potassium Channels.内向整流钾通道中的胆固醇结合位点。
Adv Exp Med Biol. 2019;1135:119-138. doi: 10.1007/978-3-030-14265-0_7.
7
Cholesterol in phospholipid bilayers: positions and orientations inside membranes with different unsaturation degrees.磷脂双层膜中的胆固醇:不同不饱和程度的膜内位置和取向。
Soft Matter. 2018 Dec 19;15(1):78-93. doi: 10.1039/c8sm01937a.
8
Cholesterol-Binding Sites in GIRK Channels: The Devil is in the Details.GIRK通道中的胆固醇结合位点:细节决定成败。
Lipid Insights. 2018 Feb 14;11:1178635317754071. doi: 10.1177/1178635317754071. eCollection 2018.
9
Dual activation of neuronal G protein-gated inwardly rectifying potassium (GIRK) channels by cholesterol and alcohol.胆固醇和酒精对神经元 G 蛋白门控内向整流钾 (GIRK) 通道的双重激活。
Sci Rep. 2017 Jul 4;7(1):4592. doi: 10.1038/s41598-017-04681-x.
10
Synergistic activation of G protein-gated inwardly rectifying potassium channels by cholesterol and PI(4,5)P.胆固醇和 PI(4,5)P 协同激活 G 蛋白门控内向整流钾通道。
Biochim Biophys Acta Biomembr. 2017 Jul;1859(7):1233-1241. doi: 10.1016/j.bbamem.2017.03.023. Epub 2017 Apr 1.