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脂质组学分析在铁死亡中的应用。

Lipidomics Analysis in Ferroptosis.

机构信息

Department of Pediatrics, The Third Xiangya Hospital Central South University, Changsha, Hunan, China.

出版信息

Methods Mol Biol. 2023;2712:149-156. doi: 10.1007/978-1-0716-3433-2_13.

DOI:10.1007/978-1-0716-3433-2_13
PMID:37578703
Abstract

Ferroptosis is a form of regulated cell death that occurs due to abnormal lipid metabolism. Lipids, which have been identified in over 45,000 different molecular species, play essential roles in modulating basic life processes. The process of ferroptosis is highly reliant on various lipid species, with polyunsaturated fatty acids (PUFAs) playing a central role in driving this process. Recent advances in mass spectrometry-based lipidomics have led to a surge in studies on ferroptosis. To explore the mechanism of lipid homeostasis in ferroptosis, the development of lipidomics techniques is critical. Currently, liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC-MS) are the most widely used analytical techniques in lipidomics. These techniques offer deeper insights into the complex lipid mechanisms that underlie ferroptosis.

摘要

铁死亡是一种由于脂质代谢异常导致的细胞程序性死亡形式。脂质在超过 45000 种不同的分子物种中被鉴定出来,在调节基本生命过程中发挥着至关重要的作用。铁死亡过程高度依赖于各种脂质物种,其中多不饱和脂肪酸(PUFAs)在驱动这一过程中起着核心作用。基于质谱的脂质组学的最新进展导致了铁死亡研究的激增。为了探索铁死亡中脂质动态平衡的机制,脂质组学技术的发展至关重要。目前,液相色谱-串联质谱(LC-MS/MS)和气相色谱-质谱(GC-MS)是脂质组学中最广泛使用的分析技术。这些技术提供了对铁死亡背后复杂脂质机制的更深入了解。

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本文引用的文献

1
The lipid flippase SLC47A1 blocks metabolic vulnerability to ferroptosis.脂质翻转酶 SLC47A1 阻断代谢易感性的铁死亡。
Nat Commun. 2022 Dec 27;13(1):7965. doi: 10.1038/s41467-022-35707-2.
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Guiding the choice of informatics software and tools for lipidomics research applications.指导脂质组学研究应用中信息学软件和工具的选择。
Nat Methods. 2023 Feb;20(2):193-204. doi: 10.1038/s41592-022-01710-0. Epub 2022 Dec 21.
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Mass spectrometry-based metabolomics: a guide for annotation, quantification and best reporting practices.
基于质谱的代谢组学:注释、定量和最佳报告实践指南。
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Lipid Metabolism in Ferroptosis.铁死亡中的脂质代谢。
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Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis.氧化的花生四烯酸和肾上腺酸磷脂酰乙醇胺引导细胞走向铁死亡。
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Identification of ACSL4 as a biomarker and contributor of ferroptosis.鉴定ACSL4作为铁死亡的生物标志物和促成因素。
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Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis.脂氧合酶对多不饱和脂肪酸的过氧化作用驱动铁死亡。
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