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线粒体复合物 I 在低氧条件下产生的活性氧和氧化还原信号转导。

Mitochondrial complex I ROS production and redox signaling in hypoxia.

机构信息

Department of Anesthesiology and Perioperative Medicine, University of Rochester Medical Center, Rochester, NY, 14642, USA.

Department of Neurobiology, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Redox Biol. 2023 Nov;67:102926. doi: 10.1016/j.redox.2023.102926. Epub 2023 Oct 16.

DOI:10.1016/j.redox.2023.102926
PMID:37871533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10598411/
Abstract

Mitochondria are a main source of cellular energy. Oxidative phosphorylation (OXPHOS) is the major process of aerobic respiration. Enzyme complexes of the electron transport chain (ETC) pump protons to generate a protonmotive force (Δp) that drives OXPHOS. Complex I is an electron entry point into the ETC. Complex I oxidizes nicotinamide adenine dinucleotide (NADH) and transfers electrons to ubiquinone in a reaction coupled with proton pumping. Complex I also produces reactive oxygen species (ROS) under various conditions. The enzymatic activities of complex I can be regulated by metabolic conditions and serves as a regulatory node of the ETC. Complex I ROS plays diverse roles in cell metabolism ranging from physiologic to pathologic conditions. Progress in our understanding indicates that ROS release from complex I serves important signaling functions. Increasing evidence suggests that complex I ROS is important in signaling a mismatch in energy production and demand. In this article, we review the role of ROS from complex I in sensing acute hypoxia.

摘要

线粒体是细胞能量的主要来源。氧化磷酸化(OXPHOS)是有氧呼吸的主要过程。电子传递链(ETC)的酶复合物将质子泵出以产生质子动力势(Δp),从而驱动 OXPHOS。复合物 I 是电子进入 ETC 的入口点。复合物 I 将烟酰胺腺嘌呤二核苷酸(NADH)氧化,并在与质子泵出偶联的反应中将电子转移给泛醌。复合物 I 在各种条件下还会产生活性氧物质(ROS)。在代谢条件下,复合物 I 的酶活性可以被调节,并且作为 ETC 的调节节点。复合物 I ROS 在细胞代谢中发挥着从生理到病理条件的多种作用。研究的进展表明,复合物 I 的 ROS 释放具有重要的信号功能。越来越多的证据表明,复合物 I ROS 对于感应能量产生和需求之间的不匹配很重要。在本文中,我们综述了 ROS 从复合物 I 中释放出来在感知急性缺氧中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/021207f75059/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/c97c54b5a0e7/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/2ee49fff01a7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/c35a3af4c6e4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/212f18de5459/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/021207f75059/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/c97c54b5a0e7/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/2ee49fff01a7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/c35a3af4c6e4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/212f18de5459/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec55/10598411/021207f75059/gr4.jpg

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