Oxidized phospholipids in ferroptosis, immunity and inflammation

Redox Biochemistry and Chemistry Pub Date : 2025-12-01 Epub Date: 2025-10-09 DOI:10.1016/j.rbc.2025.100061
Valerie B. O'Donnell , Valery Bochkov
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Abstract

Oxidized phospholipids (oxPL) are generated by enzymatic or non-enzymatic reactions and play diverse roles in immunity and inflammation. OxPL are elevated in tissues from many human diseases and are now recognized as endogenous damage-associated molecular patterns (DAMPs) that alert the immune system to challenge. Early studies focused on the role(s) of non-enzymatically-formed oxPCs in cardiovascular disease, while more recently, the controlled generation of enzymatically-oxidized PL (eoxPL) in blood cells and their participation in physiological hemostasis has been delineated. In the last decade, there has been an explosion of research into their formation and roles in ferroptosis, a form of cell death driven by iron and lipid oxidation. This mini review aims to bring the reader up to date with recent work in this area, focused on discoveries over the last few years that firmly extend our knowledge of the roles of oxPL as mediators of ferroptosis, innate and adaptive immunity.
氧化磷脂在铁下垂、免疫和炎症中的作用
氧化磷脂(oxPL)是由酶促或非酶促反应产生的,在免疫和炎症中发挥着多种作用。OxPL在许多人类疾病的组织中升高,现在被认为是内源性损伤相关分子模式(DAMPs),提醒免疫系统进行挑战。早期的研究集中在非酶形成的氧化酶在心血管疾病中的作用,而最近,血细胞中酶氧化PL (eoxPL)的受控生成及其在生理止血中的参与已经被描述。在过去的十年中,对它们的形成和在铁死亡中的作用的研究激增,铁死亡是一种由铁和脂质氧化驱动的细胞死亡形式。这篇迷你综述的目的是让读者了解这一领域最近的工作,重点是过去几年的发现,这些发现坚定地扩展了我们对oxPL作为铁死亡、先天和适应性免疫介质的作用的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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