GPx4在细菌感染和多微生物脓毒症中的作用:与铁亡和焦亡有关。

Hong Zhu, Arben Santo, Zhenquan Jia, Y Robert Li
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引用次数: 51

摘要

虽然众所周知,细菌感染是脓毒症的主要原因,但这种临床综合征的分子病理生理学仍然不明确。在这篇研究重点文章中,我们讨论了关于谷胱甘肽过氧化物酶-4 (GPx4)通过调节铁亡和焦亡(两种新的调节细胞死亡模式)在细菌感染和多微生物脓毒症中的保护作用的最新研究发现。提示GPx4作为铁下垂和焦下垂的必要通道,可能是开发有效的感染和脓毒症控制药物的关键分子靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

GPx4 in Bacterial Infection and Polymicrobial Sepsis: Involvement of Ferroptosis and Pyroptosis.

GPx4 in Bacterial Infection and Polymicrobial Sepsis: Involvement of Ferroptosis and Pyroptosis.

While it is well known that bacterial infection is the predominant cause of sepsis, the molecular pathophysiology of this clinical syndrome remains ill-defined. In this Research Highlights article, we discuss the recent research findings regarding a protective role for glutathione peroxidase-4 (GPx4) in bacterial infection and polymicrobial sepsis via modulating ferroptosis and pyroptosis, two novel modes of regulated cell death. It is suggested that GPx4, being a requisite gateway to both ferroptosis and pyroptosis, may serve as a critical molecular target for developing effective drugs for controlling infection and sepsis.

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