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铁死亡的细胞生物学。

The cell biology of ferroptosis.

机构信息

Department of Biology, Stanford University, Stanford, CA, USA.

Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.

出版信息

Nat Rev Mol Cell Biol. 2024 Jun;25(6):424-442. doi: 10.1038/s41580-024-00703-5. Epub 2024 Feb 16.

Abstract

Ferroptosis is a non-apoptotic cell death mechanism characterized by iron-dependent membrane lipid peroxidation. Here, we review what is known about the cellular mechanisms mediating the execution and regulation of ferroptosis. We first consider how the accumulation of membrane lipid peroxides leads to the execution of ferroptosis by altering ion transport across the plasma membrane. We then discuss how metabolites and enzymes that are distributed in different compartments and organelles throughout the cell can regulate sensitivity to ferroptosis by impinging upon iron, lipid and redox metabolism. Indeed, metabolic pathways that reside in the mitochondria, endoplasmic reticulum, lipid droplets, peroxisomes and other organelles all contribute to the regulation of ferroptosis sensitivity. We note how the regulation of ferroptosis sensitivity by these different organelles and pathways seems to vary between different cells and death-inducing conditions. We also highlight transcriptional master regulators that integrate the functions of different pathways and organelles to modulate ferroptosis sensitivity globally. Throughout this Review, we highlight open questions and areas in which progress is needed to better understand the cell biology of ferroptosis.

摘要

铁死亡是一种非细胞凋亡的细胞死亡机制,其特征是铁依赖性的膜脂质过氧化。在这里,我们回顾了介导铁死亡执行和调控的细胞机制。我们首先考虑了膜脂质过氧化物的积累如何通过改变质膜的离子转运来导致铁死亡的执行。然后,我们讨论了如何通过影响铁、脂质和氧化还原代谢,分布在细胞不同区室和细胞器中的代谢物和酶来调节对铁死亡的敏感性。事实上,位于线粒体、内质网、脂滴、过氧化物酶体和其他细胞器中的代谢途径都有助于调节铁死亡敏感性。我们注意到,不同细胞器和途径对铁死亡敏感性的调节似乎在不同的细胞和诱导死亡的条件下有所不同。我们还强调了转录主控调节剂,它们整合了不同途径和细胞器的功能,以全局调节铁死亡敏感性。在本综述中,我们强调了一些开放性问题和需要取得进展的领域,以更好地理解铁死亡的细胞生物学。

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