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内向整流钾通道Kir4.2的生理特性及其在人类疾病中的研究进展

The physiological characteristics of inward rectifying potassium channel Kir4.2 and its research progress in human diseases.

作者信息

Zhang Hongling, Bai Zhongyuan, Xi Yanfeng

机构信息

Pathology Department, The Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China.

Colorectal Surgery, The First Clinical Medical College of Shanxi Medical University, Taiyuan, China.

出版信息

Front Cell Dev Biol. 2025 Apr 24;13:1519080. doi: 10.3389/fcell.2025.1519080. eCollection 2025.

DOI:10.3389/fcell.2025.1519080
PMID:40342929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12058739/
Abstract

Kir4.2 is a member of the inward rectifying potassium channel family, encoded by the KCNJ15 gene. The Kir4.2 protein is expressed in various organs including the kidneys, liver, pancreas, bladder, stomach, and lungs. Kir4.2 not only forms functional homomeric channels, but also heteromeric channels with Kir5.1. An increasing number of studies indicate that the function of the Kir4.2 channel should not be underestimated. Kir4.2 participates in cell electrotaxis chemotaxis by sensing extracellular electric fields and functions as a K + sensor in the proximal tubules of the kidney, playing a crucial role in maintaining acid-base and potassium balance. This article provides a comprehensive review of the main physiological characteristics of the Kir4.2 channel, the various pathological processes it is involved in, and the human diseases resulting from Kir4.2 dysfunction.

摘要

Kir4.2是内向整流钾通道家族的成员,由KCNJ15基因编码。Kir4.2蛋白在包括肾脏、肝脏、胰腺、膀胱、胃和肺在内的各种器官中表达。Kir4.2不仅形成功能性同聚体通道,还与Kir5.1形成异聚体通道。越来越多的研究表明,Kir4.2通道的功能不容小觑。Kir4.2通过感知细胞外电场参与细胞电趋化性趋化作用,并在肾脏近端小管中作为钾离子传感器发挥作用,在维持酸碱和钾平衡方面起着关键作用。本文全面综述了Kir4.2通道的主要生理特性、其参与的各种病理过程以及Kir4.2功能障碍导致的人类疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f77e/12058739/ac320d9cb972/fcell-13-1519080-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f77e/12058739/b1753d5d2f34/fcell-13-1519080-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f77e/12058739/ac320d9cb972/fcell-13-1519080-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f77e/12058739/b1753d5d2f34/fcell-13-1519080-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f77e/12058739/ac320d9cb972/fcell-13-1519080-g002.jpg

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Nat Commun. 2024 Jun 17;15(1):5144. doi: 10.1038/s41467-024-49562-w.
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Paxillin/HDAC6 regulates microtubule acetylation to promote directional migration of keratinocytes driven by electric fields.桩蛋白/HDAC6 通过调控微管乙酰化促进电场驱动的角质形成细胞的定向迁移。
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COL3A1-positive endothelial cells influence LUAD prognosis and regulate LUAD carcinogenesis by NCL-PI3K-AKT axis.
COL3A1 阳性内皮细胞通过 NCL-PI3K-AKT 轴影响 LUAD 预后并调节 LUAD 癌变。
J Gene Med. 2024 Jan;26(1):e3573. doi: 10.1002/jgm.3573. Epub 2023 Aug 7.
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Screening and validation of potential markers associated with uterine corpus endometrial carcinoma and polycystic ovary syndrome based on bioinformatics methods.基于生物信息学方法的子宫内膜癌和多囊卵巢综合征相关潜在标志物的筛选与验证
Front Mol Biosci. 2023 Jun 9;10:1192313. doi: 10.3389/fmolb.2023.1192313. eCollection 2023.
5
KCNJ15 deficiency promotes drug resistance via affecting the function of lysosomes.钾通道蛋白KCNJ15缺陷通过影响溶酶体功能促进耐药性。
Asian J Pharm Sci. 2023 May;18(3):100814. doi: 10.1016/j.ajps.2023.100814. Epub 2023 May 12.
6
Exploring the common diagnostic gene KCNJ15 and shared pathway of ankylosing spondylitis and ulcerative colitis through integrated bioinformatics.通过综合生物信息学探索强直性脊柱炎和溃疡性结肠炎的共同诊断基因KCNJ15及共享通路。
Front Physiol. 2023 May 5;14:1146538. doi: 10.3389/fphys.2023.1146538. eCollection 2023.
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Front Oncol. 2023 Jan 10;12:1074469. doi: 10.3389/fonc.2022.1074469. eCollection 2022.
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