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

GPx4 in Bacterial Infection and Polymicrobial Sepsis: Involvement of Ferroptosis and Pyroptosis.
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DOI:
10.20455/ros.2019.835
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发表时间:
2019-05-01
期刊:
Reactive oxygen species (Apex, N.C.)
影响因子:
--
通讯作者:
Robert Li, Y
Robert Li, Y
中科院分区:
其他
文献类型:
--
作者:
Zhu, Hong;Santo, Arben;Robert Li, Y

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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不清楚。在这篇研究亮点文章中,我们讨论了最近的研究结果,即谷胱甘肽过氧化物酶-4(Gpx4)通过调节铁下垂和下垂在细菌感染和多菌败血症中的保护作用,这是调节细胞死亡的两种新模式。提示Gpx4是铁性下垂和下睑下垂的必经通道,可作为开发有效控制感染和败血症药物的重要分子靶点。
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.