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线粒体硫氧还蛋白的昼夜节律波动。

Circadian Oscillation of Sulfiredoxin in the Mitochondria.

机构信息

Yonsei Biomedical Research Institute, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Korea.

Yonsei Biomedical Research Institute, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Korea.

出版信息

Mol Cell. 2015 Aug 20;59(4):651-63. doi: 10.1016/j.molcel.2015.06.031. Epub 2015 Jul 30.

Abstract

Hydrogen peroxide (H2O2) released from mitochondria regulates various cell signaling pathways. Given that H2O2-eliminating enzymes such as peroxiredoxin III (PrxIII) are abundant in mitochondria, however, it has remained unknown how such release can occur. Active PrxIII-SH undergoes reversible inactivation via hyperoxidation to PrxIII-SO2, which is then reduced by sulfiredoxin. We now show that the amounts of PrxIII-SO2 and sulfiredoxin undergo antiphasic circadian oscillation in the mitochondria of specific tissues of mice maintained under normal conditions. Cytosolic sulfiredoxin was found to be imported into the mitochondria via a mechanism that requires formation of a disulfide-linked complex with heat shock protein 90, which is promoted by H2O2 released from mitochondria. The imported sulfiredoxin is degraded by Lon in a manner dependent on PrxIII hyperoxidation state. The coordinated import and degradation of sulfiredoxin provide the basis for sulfiredoxin oscillation and consequent PrxIII-SO2 oscillation in mitochondria and likely result in an oscillatory H2O2 release.

摘要

过氧化氢(H2O2)从线粒体中释放出来,调节着各种细胞信号通路。然而,鉴于线粒体中含有大量的过氧化氢清除酶,如过氧化物还原酶 III(PrxIII),这种释放是如何发生的仍然未知。活性 PrxIII-SH 通过超氧化作用可逆失活,形成 PrxIII-SO2,然后被硫氧还蛋白还原。我们现在发现,在正常条件下维持的小鼠特定组织的线粒体中,PrxIII-SO2 和硫氧还蛋白的含量呈相反的昼夜节律性波动。细胞质硫氧还蛋白通过一种需要与热休克蛋白 90 形成二硫键连接复合物的机制被导入线粒体,该机制由线粒体释放的 H2O2 促进。导入的硫氧还蛋白被 Lon 降解,这一过程依赖于 PrxIII 的超氧化状态。硫氧还蛋白的协调导入和降解为硫氧还蛋白的波动以及随后的线粒体中 PrxIII-SO2 的波动提供了基础,这可能导致 H2O2 的释放呈振荡性。

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