Hypoxia-inducible factor 1: regulator of mitochondrial metabolism and mediator of ischemic preconditioning.

Hypoxia-inducible factor 1: regulator of mitochondrial metabolism and mediator of ischemic preconditioning.
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DOI:
10.1016/j.bbamcr.2010.08.006
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发表时间:
2011-07
期刊:
Biochimica et biophysica acta
影响因子:
--
通讯作者:
Semenza GL
Semenza GL
中科院分区:
其他
文献类型:
--
作者:
Semenza GL

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缺氧诱导因子 1 (HIF-1) 通过调节基因表达来介导对氧气可用性降低的适应性反应。 HIF-1 控制的慢性缺氧的关键细胞自主适应性反应是线粒体质量和/或代谢减少。 HIF-1 缺陷的成纤维细胞暴露于慢性缺氧会导致细胞因活性氧 (ROS) 水平过高而死亡。 HIF-1 通过多种机制减少缺氧条件下 ROS 的产生,包括:细胞色素 c 氧化酶中的亚基从 COX4-1 调节亚基转换为 COX4-2 调节亚基,从而提高复合物 IV 的效率;诱导丙酮酸脱氢酶激酶 1,将丙酮酸从线粒体中分流出来;诱导 BNIP3,触发线粒体选择性自噬; microRNA-210 的诱导,阻止氧化磷酸化所需的 Fe/S 簇的组装。 HIF-1 也是缺血预处理所必需的,这种作用可能部分归因于它对 CD73(一种产生腺苷的酶)的诱导。 HIF-1 依赖性线粒体代谢调节也可能有助于缺血预处理的保护作用。
Hypoxia-inducible factor 1 (HIF-1) mediates adaptive responses to reduced oxygen availability by regulating gene expression. A critical cell-autonomous adaptive response to chronic hypoxia controlled by HIF-1 is reduced mitochondrial mass and/or metabolism. Exposure of HIF-1-deficient fibroblasts to chronic hypoxia results in cell death due to excessive levels of reactive oxygen species (ROS). HIF-1 reduces ROS production under hypoxic conditions by multiple mechanisms including: a subunit switch in cytochrome c oxidase from the COX4-1 to COX4-2 regulatory subunit that increases the efficiency of complex IV; induction of pyruvate dehydrogenase kinase 1, which shunts pyruvate away from the mitochondria; induction of BNIP3, which triggers mitochondrial selective autophagy; and induction of microRNA-210, which blocks assembly of Fe/S clusters that are required for oxidative phosphorylation. HIF-1 is also required for ischemic preconditioning and this effect may be due in part to its induction of CD73, the enzyme that produces adenosine. HIF-1-dependent regulation of mitochondrial metabolism may also contribute to the protective effects of ischemic preconditioning.
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