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缺氧诱导的自噬:细胞死亡还是细胞存活?

Hypoxia-induced autophagy: cell death or cell survival?

机构信息

Institute of Developmental Biology and Cancer Research, University of Nice, CNRS-UMR 6543, Centre Antoine Lacassagne, 33 Avenue de Valombrose, 06189 Nice, France.

出版信息

Curr Opin Cell Biol. 2010 Apr;22(2):177-80. doi: 10.1016/j.ceb.2009.11.015. Epub 2009 Dec 21.

Abstract

Hypoxia (approximately 3-0.1% oxygen) is capable of rapidly inducing, via the hypoxia-inducible factor (HIF-1), a cell survival response engaging autophagy. This process is mediated by the atypical BH3-only proteins the Bcl-2/E1B 19kDa-interacting protein 3 (BNIP3/BNIP3L (NIX)) that are induced by HIF-1. These mitochondrial associated BNIP proteins also mediate mitophagy, a metabolic adaptation for survival that is able to control reactive oxygen species (ROS) production and DNA damage. In contrast, severe hypoxic conditions or anoxia (<0.1% oxygen), where the latter is often confused with physiological hypoxia, are capable of inducing a HIF-independent autophagic response, generated via an extreme nutritional stress response implicating the AMPK-mTOR and unfolded protein response (UPR) pathways. The autophagic cell death that is often observed in these extreme stress conditions should be seen as the outcome of failed adaptation.

摘要

缺氧(约 3-0.1%氧气)能够通过缺氧诱导因子(HIF-1)迅速诱导细胞存活反应,涉及自噬。这个过程是由非典型 BH3 仅蛋白 Bcl-2/E1B 19kDa 相互作用蛋白 3(BNIP3/BNIP3L(NIX))介导的,HIF-1 诱导这些线粒体相关的 BNIP 蛋白也介导了线粒体自噬,这是一种生存的代谢适应,能够控制活性氧(ROS)的产生和 DNA 损伤。相比之下,严重的缺氧条件或缺氧(<0.1%氧气),后者常与生理性缺氧混淆,能够诱导一种 HIF 非依赖性的自噬反应,这种反应是通过涉及 AMPK-mTOR 和未折叠蛋白反应(UPR)途径的极端营养应激反应产生的。在这些极端应激条件下经常观察到的自噬性细胞死亡,应被视为适应失败的结果。

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