Institute of Developmental Biology and Cancer Research, University of Nice, CNRS-UMR 6543, Centre Antoine Lacassagne, 33 Avenue de Valombrose, 06189 Nice, France.
Curr Opin Cell Biol. 2010 Apr;22(2):177-80. doi: 10.1016/j.ceb.2009.11.015. Epub 2009 Dec 21.
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.
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。