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Nat Commun. 2018 Jul 19;9(1):2815. doi: 10.1038/s41467-018-05043-5.
2
Tissue Distribution of Kir7.1 Inwardly Rectifying K Channel Probed in a Knock-in Mouse Expressing a Haemagglutinin-Tagged Protein.在表达血凝素标记蛋白的敲入小鼠中对Kir7.1内向整流钾通道进行组织分布研究
Front Physiol. 2018 Apr 23;9:428. doi: 10.3389/fphys.2018.00428. eCollection 2018.
3
Oxytocin (OXT)-stimulated inhibition of Kir7.1 activity is through PIP-dependent Ca response of the oxytocin receptor in the retinal pigment epithelium in vitro.在体外,催产素(OXT)刺激的 Kir7.1 活性抑制是通过视网膜色素上皮细胞中催产素受体的 PIP 依赖性 Ca 反应实现的。
Cell Signal. 2017 Sep;37:93-102. doi: 10.1016/j.cellsig.2017.06.005. Epub 2017 Jun 8.
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J Immunol Methods. 2017 Jun;445:53-58. doi: 10.1016/j.jim.2017.03.008. Epub 2017 Mar 12.
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Elife. 2017 Jan 16;6:e24149. doi: 10.7554/eLife.24149.
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Structure of a Pancreatic ATP-Sensitive Potassium Channel.胰腺 ATP 敏感性钾通道的结构。
Cell. 2017 Jan 12;168(1-2):101-110.e10. doi: 10.1016/j.cell.2016.12.028.
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A Common Signal Patch Drives AP-1 Protein-dependent Golgi Export of Inwardly Rectifying Potassium Channels.一个共同的信号补丁驱动内向整流钾通道的AP-1蛋白依赖性高尔基体输出。
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Multiple Sclerosis and Antibodies against KIR4.1.多发性硬化症与抗KIR4.1抗体
N Engl J Med. 2016 Apr 14;374(15):1496-8. doi: 10.1056/NEJMc1507131.
9
A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).一种新型的KCNJ13无义突变及Kir7.1通道功能丧失导致莱伯先天性黑蒙(LCA16)。
Hum Mutat. 2015 Jul;36(7):720-7. doi: 10.1002/humu.22807. Epub 2015 May 20.
10
G-protein-independent coupling of MC4R to Kir7.1 in hypothalamic neurons.下丘脑神经元中黑皮质素4受体(MC4R)与内向整流型钾通道7.1(Kir7.1)的非G蛋白偶联
Nature. 2015 Apr 2;520(7545):94-8. doi: 10.1038/nature14051. Epub 2015 Jan 19.

G 蛋白偶联受体差异调节内向整流钾通道 Kir7.1 的糖基化和活性。

G protein-coupled receptors differentially regulate glycosylation and activity of the inwardly rectifying potassium channel Kir7.1.

机构信息

From the Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee 37232; Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109.

Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109.

出版信息

J Biol Chem. 2018 Nov 16;293(46):17739-17753. doi: 10.1074/jbc.RA118.003238. Epub 2018 Sep 26.

DOI:10.1074/jbc.RA118.003238
PMID:30257863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6240878/
Abstract

Kir7.1 is an inwardly rectifying potassium channel with important roles in the regulation of the membrane potential in retinal pigment epithelium, uterine smooth muscle, and hypothalamic neurons. Regulation of G protein-coupled inwardly rectifying potassium (GIRK) channels by G protein-coupled receptors (GPCRs) via the G protein βγ subunits has been well characterized. However, how Kir channels are regulated is incompletely understood. We report here that Kir7.1 is also regulated by GPCRs, but through a different mechanism. Using Western blotting analysis, we observed that multiple GPCRs tested caused a striking reduction in the complex glycosylation of Kir7.1. Further, GPCR-mediated reduction of Kir7.1 glycosylation in HEK293T cells did not alter its expression at the cell surface but decreased channel activity. Of note, mutagenesis of the sole Kir7.1 glycosylation site reduced conductance and open probability, as indicated by single-channel recording. Additionally, we report that the L241P mutation of Kir7.1 associated with Lebers congenital amaurosis (LCA), an inherited retinal degenerative disease, has significantly reduced complex glycosylation. Collectively, these results suggest that Kir7.1 channel glycosylation is essential for function, and this activity within cells is suppressed by most GPCRs. The melanocortin-4 receptor (MC4R), a GPCR previously reported to induce ligand-regulated activity of this channel, is the only GPCR tested that does not have this effect on Kir7.1.

摘要

Kir7.1 是一种内向整流钾通道,在视网膜色素上皮、子宫平滑肌和下丘脑神经元的膜电位调节中具有重要作用。G 蛋白偶联受体 (GPCR) 通过 G 蛋白 βγ 亚基对 G 蛋白偶联内向整流钾 (GIRK) 通道的调节已得到充分研究。然而,Kir 通道如何被调节尚不完全清楚。我们在此报告 Kir7.1 也受 GPCR 调节,但通过不同的机制。通过 Western blot 分析,我们观察到多种测试的 GPCR 导致 Kir7.1 的复杂糖基化明显减少。此外,GPCR 介导的 HEK293T 细胞中 Kir7.1 糖基化的减少并未改变其在细胞表面的表达,但降低了通道活性。值得注意的是,Kir7.1 上唯一的糖基化位点的突变降低了电导和开放概率,如单通道记录所示。此外,我们报告与 Leber 先天性黑蒙 (LCA) 相关的 Kir7.1 的 L241P 突变显著降低了其复杂糖基化。总之,这些结果表明 Kir7.1 通道糖基化对于功能至关重要,而细胞内的这种活性受到大多数 GPCR 的抑制。黑皮质素-4 受体 (MC4R) 是一种先前报道可诱导该通道配体调节活性的 GPCR,是唯一一种对 Kir7.1 没有这种作用的 GPCR。