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