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氯离子通道在消化系统疾病中的作用(综述)

The function of chloride channels in digestive system disease (Review).

作者信息

Hu Yanxia, Tuo Biguang

机构信息

Department of Gastroenterology, Digestive Disease Hospital, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou 563000, P.R. China.

出版信息

Int J Mol Med. 2025 Jun;55(6). doi: 10.3892/ijmm.2025.5540. Epub 2025 May 2.

DOI:10.3892/ijmm.2025.5540
PMID:40314091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12045473/
Abstract

Cation channels have been extensively studied in the context of digestive disorders, but comparatively little attention has been given to anions and their associated channels. Chloride ions, the most abundant anions in the human body, act as signaling molecules, modulating cellular behavior and playing a key role in regulating multiorgan physiological and pathophysiological mechanisms. The intra‑ and extracellular distributions of chloride ions are primarily controlled by various chloride channels and transporters. Currently, these chloride channels are classified into several groups: The chloride channels family, cystic fibrosis transmembrane conductance regulator, calcium‑activated chloride channels, volume‑regulated anion channels, proton‑activated chloride channels and ligand‑gated anion channels. This review aims to summarize the roles of chloride ion channels and transporter proteins in digestive system diseases, providing a theoretical basis for future research and offering potential new strategies for disease treatment.

摘要

阳离子通道在消化系统疾病背景下已得到广泛研究,但阴离子及其相关通道相对较少受到关注。氯离子是人体中最丰富的阴离子,作为信号分子,调节细胞行为,并在调节多器官生理和病理生理机制中发挥关键作用。氯离子的细胞内和细胞外分布主要由各种氯离子通道和转运体控制。目前,这些氯离子通道分为几组:氯离子通道家族、囊性纤维化跨膜传导调节因子、钙激活氯离子通道、容积调节性阴离子通道、质子激活氯离子通道和配体门控阴离子通道。本综述旨在总结氯离子通道和转运蛋白在消化系统疾病中的作用,为未来研究提供理论基础,并为疾病治疗提供潜在的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/4e14750db0ff/ijmm-55-06-05540-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/7c30f33cbbf6/ijmm-55-06-05540-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/53a826a34b58/ijmm-55-06-05540-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/4e14750db0ff/ijmm-55-06-05540-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/7c30f33cbbf6/ijmm-55-06-05540-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/53a826a34b58/ijmm-55-06-05540-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99d/12045473/4e14750db0ff/ijmm-55-06-05540-g02.jpg

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Int J Exp Pathol. 2024 Aug;105(4):118-132. doi: 10.1111/iep.12513. Epub 2024 Jul 11.
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High ANO1 expression is a prognostic factor and correlated with an immunosuppressive tumor microenvironment in pancreatic cancer.ANO1 高表达是胰腺癌的一个预后因素,并与免疫抑制性肿瘤微环境相关。
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Epithelial TNF controls cell differentiation and CFTR activity to maintain intestinal mucin homeostasis.
上皮细胞 TNF 控制细胞分化和 CFTR 活性以维持肠道粘蛋白的动态平衡。
J Clin Invest. 2023 Oct 16;133(20):e163591. doi: 10.1172/JCI163591.
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LRRC8A promotes the initial development of oxaliplatin resistance in colon cancer cells.LRRC8A促进结肠癌细胞中奥沙利铂耐药性的初始发展。
Heliyon. 2023 Jun 1;9(6):e16872. doi: 10.1016/j.heliyon.2023.e16872. eCollection 2023 Jun.
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LRRC8A is responsible for exosome biogenesis and volume regulation in colon cancer cells.LRRC8A 负责结肠癌细胞外体的生物发生和体积调节。
Biochem J. 2023 May 17;480(9):701-713. doi: 10.1042/BCJ20220614.
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ClC-K Kidney Chloride Channels: From Structure to Pathology.ClC-K 肾脏氯离子通道:从结构到病理学。
Handb Exp Pharmacol. 2024;283:35-58. doi: 10.1007/164_2023_635.
7
Proton-Activated Chloride Channel: Physiology and Disease.质子激活氯离子通道:生理学与疾病。
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8
Hepatocyte-specific TMEM16A deficiency alleviates hepatic ischemia/reperfusion injury via suppressing GPX4-mediated ferroptosis.肝特异性 TMEM16A 缺乏通过抑制 GPX4 介导的铁死亡缓解肝缺血/再灌注损伤。
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