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大孔通道在微生物诱导的炎症中的作用。

Contribution of large-pore channels to inflammation induced by microorganisms.

作者信息

Vega José L, Gutiérrez Camila, Rojas Mauro, Güiza Juan, Sáez Juan C

机构信息

Laboratory of Gap Junctions Proteins and Parasitic Diseases (GaPaL), Instituto Antofagasta, Universidad de Antofagasta, Antofagasta, Chile.

Centro de Investigación en Inmunología y Biotecnología Biomédica de Antofagasta (CIIBBA), Universidad de Antofagasta, Antofagasta, Chile.

出版信息

Front Cell Dev Biol. 2023 Jan 9;10:1094362. doi: 10.3389/fcell.2022.1094362. eCollection 2022.

DOI:10.3389/fcell.2022.1094362
PMID:36699007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9868820/
Abstract

Plasma membrane ionic channels selectively permeate potassium, sodium, calcium, and chloride ions. However, large-pore channels are permeable to ions and small molecules such as ATP and glutamate, among others. Large-pore channels are structures formed by several protein families with little or no evolutionary linkages including connexins (Cxs), pannexins (Panxs), innexin (Inxs), unnexins (Unxs), calcium homeostasis modulator (CALHMs), and Leucine-rich repeat-containing 8 (LRRC8) proteins. Large-pore channels are key players in inflammatory cell response, guiding the activation of inflammasomes, the release of pro-inflammatory cytokines such as interleukin-1 beta (IL-1ß), and the release of adenosine-5'-triphosphate (ATP), which is considered a danger signal. This review summarizes our current understanding of large-pore channels and their contribution to inflammation induced by microorganisms, virulence factors or their toxins.

摘要

质膜离子通道可选择性地通透钾离子、钠离子、钙离子和氯离子。然而,大孔通道可通透离子以及诸如ATP和谷氨酸等小分子。大孔通道是由几个蛋白质家族形成的结构,这些家族之间几乎没有或没有进化联系,包括连接蛋白(Cxs)、泛连接蛋白(Panxs)、间隙连接蛋白(Inxs)、非连接蛋白(Unxs)、钙稳态调节剂(CALHMs)和富含亮氨酸重复序列8(LRRC8)蛋白。大孔通道是炎症细胞反应的关键参与者,指导炎性小体的激活、促炎细胞因子如白细胞介素-1β(IL-1β)的释放以及被视为危险信号的腺苷-5'-三磷酸(ATP)的释放。本综述总结了我们目前对大孔通道及其在微生物、毒力因子或其毒素诱导的炎症中所起作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea96/9868820/1ad366ddd2a7/fcell-10-1094362-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea96/9868820/1ad366ddd2a7/fcell-10-1094362-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea96/9868820/1ad366ddd2a7/fcell-10-1094362-g001.jpg

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1
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本文引用的文献

1
Ion channel molecular complexes in vascular smooth muscle.血管平滑肌中的离子通道分子复合物
Front Physiol. 2022 Aug 26;13:999369. doi: 10.3389/fphys.2022.999369. eCollection 2022.
2
Role of Pannexin-1-P2X7R signaling on cell death and pro-inflammatory mediator expression induced by toxins in enteric glia.缝隙连接蛋白 1-P2X7R 信号通路在毒素诱导肠神经胶质细胞死亡和促炎介质表达中的作用。
Front Immunol. 2022 Aug 22;13:956340. doi: 10.3389/fimmu.2022.956340. eCollection 2022.
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Cryo-EM structure of the heptameric calcium homeostasis modulator 1 channel.
七聚体钙稳态调节剂 1 通道的冷冻电镜结构。
J Biol Chem. 2022 May;298(5):101838. doi: 10.1016/j.jbc.2022.101838. Epub 2022 Mar 24.
4
The volume-regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling.LRRC8C 调控性阴离子通道通过调节环二核苷酸转运和 STING-p53 信号通路抑制 T 细胞功能。
Nat Immunol. 2022 Feb;23(2):287-302. doi: 10.1038/s41590-021-01105-x. Epub 2022 Feb 1.
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Dickkopf proteins in pathological inflammatory diseases.Dickkopf 蛋白在病理性炎症性疾病中的作用。
J Leukoc Biol. 2022 Apr;111(4):893-901. doi: 10.1002/JLB.3RI0721-385R. Epub 2021 Dec 10.
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Pannexin-1 channel opening is critical for COVID-19 pathogenesis.泛连接蛋白-1通道开放对新冠病毒发病机制至关重要。
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The spectrum of inflammatory responses.炎症反应谱。
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Unnexins: Homologs of innexin proteins in Trypanosomatidae parasites.联膜蛋白:锥虫科寄生虫中介联蛋白的同源物。
J Cell Physiol. 2022 Feb;237(2):1547-1560. doi: 10.1002/jcp.30626. Epub 2021 Nov 15.
9
Microglial Calhm2 regulates neuroinflammation and contributes to Alzheimer's disease pathology.小胶质细胞 Calhm2 调节神经炎症,并有助于阿尔茨海默病的病理。
Sci Adv. 2021 Aug 25;7(35). doi: 10.1126/sciadv.abe3600. Print 2021 Aug.
10
A physiologic rise in cytoplasmic calcium ion signal increases pannexin1 channel activity via a C-terminus phosphorylation by CaMKII.细胞质钙离子信号的生理性升高通过 CaMKII 对 C 端的磷酸化增加了连接蛋白 1 通道的活性。
Proc Natl Acad Sci U S A. 2021 Aug 10;118(32). doi: 10.1073/pnas.2108967118.