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线粒体自由基的产生与缺氧信号传导。

Mitochondrial generation of free radicals and hypoxic signaling.

作者信息

Poyton Robert O, Ball Kerri A, Castello Pablo R

机构信息

Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.

出版信息

Trends Endocrinol Metab. 2009 Sep;20(7):332-40. doi: 10.1016/j.tem.2009.04.001. Epub 2009 Sep 3.

Abstract

Most reactive oxygen species (ROS) are generated in cells by the mitochondrial respiratory chain. Mitochondrial ROS production is modulated largely by the rate of electron flow through respiratory chain complexes. Recently, it has become clear that under hypoxic conditions, the mitochondrial respiratory chain also produces nitric oxide (NO), which can generate other reactive nitrogen species (RNS). Although excess ROS and RNS can lead to oxidative and nitrosative stress, moderate to low levels of both function in cellular signaling pathways. Especially important are the roles of these mitochondrially generated free radicals in hypoxic signaling pathways, which have important implications for cancer, inflammation and a variety of other diseases.

摘要

大多数活性氧(ROS)由线粒体呼吸链在细胞中产生。线粒体ROS的产生很大程度上受通过呼吸链复合物的电子流速率调节。最近,已经明确在缺氧条件下,线粒体呼吸链也会产生一氧化氮(NO),其可生成其他活性氮物质(RNS)。尽管过量的ROS和RNS可导致氧化应激和亚硝化应激,但二者适度到低水平时在细胞信号通路中发挥作用。这些线粒体产生的自由基在缺氧信号通路中的作用尤为重要,这对癌症、炎症及多种其他疾病具有重要意义。

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