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铁死亡:生物能量代谢过程中的铁释放机制

Ferroptosis: iron release mechanisms in the bioenergetic process.

作者信息

Lee Jaewang, Roh Jong-Lyel

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, CHA Bundang Medical Center, CHA University, Seongnam, Gyeonggi-Do, 13496, Republic of Korea.

Department of Biomedical Science, General Graduate School, CHA University, Pocheon, Republic of Korea.

出版信息

Cancer Metastasis Rev. 2025 Feb 25;44(1):36. doi: 10.1007/s10555-025-10252-8.

DOI:10.1007/s10555-025-10252-8
PMID:40000477
Abstract

Ferroptosis, an iron-dependent form of cell death, has been the focus of extensive research over the past decade, leading to the elucidation of key molecules and mechanisms involved in this process. While several studies have highlighted iron sources for the Fenton reaction, the predominant mechanism for iron release in ferroptosis has been identified as ferritinophagy, which occurs in response to iron starvation. However, much of the existing literature has concentrated on lipid peroxidation rather than on the mechanisms of iron release. This review proposes three distinct mechanisms of iron mobilization: ferritinophagy, reductive pathways with selective gating of ferritin pores, and quinone-mediated iron mobilization. Notably, the latter two mechanisms operate independently of iron starvation and rely primarily on reductants such as NADH and O•. The inhibition of the respiratory chain, particularly under the activation of α-ketoglutarate dehydrogenase, leads to the accumulation of these reductants, which in turn promotes iron release from ferritin and indirectly inhibits AMP-activated protein kinase through excessive iron levels. In this work, we delineate the intricate relationship between iron mobilization and bioenergetic processes under conditions of oxidative stress. Furthermore, this review aims to enhance the understanding of the connections between ferroptosis and these mechanisms.

摘要

铁死亡是一种铁依赖性的细胞死亡形式,在过去十年中一直是广泛研究的焦点,这使得参与该过程的关键分子和机制得以阐明。虽然几项研究强调了芬顿反应的铁来源,但铁死亡中铁释放的主要机制已被确定为铁自噬,它发生在对铁饥饿的反应中。然而,现有文献大多集中在脂质过氧化而非铁释放机制上。本综述提出了三种不同的铁动员机制:铁自噬、铁蛋白孔选择性门控的还原途径和醌介导的铁动员。值得注意的是,后两种机制独立于铁饥饿起作用,主要依赖于NADH和O•等还原剂。呼吸链的抑制,特别是在α-酮戊二酸脱氢酶激活的情况下,会导致这些还原剂的积累,进而促进铁从铁蛋白中释放,并通过过量的铁水平间接抑制AMP激活的蛋白激酶。在这项工作中,我们描绘了氧化应激条件下铁动员与生物能量过程之间的复杂关系。此外,本综述旨在增进对铁死亡与这些机制之间联系的理解。

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本文引用的文献

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Adipocyte-derived ferroptotic signaling mitigates obesity.脂肪细胞衍生的铁死亡信号减轻肥胖。
Cell Metab. 2025 Mar 4;37(3):673-691.e7. doi: 10.1016/j.cmet.2024.11.010. Epub 2024 Dec 26.
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Hyperglycemia-triggered lipid peroxidation destabilizes STAT4 and impairs anti-viral Th1 responses in type 2 diabetes.高血糖引发的脂质过氧化作用会使信号转导和转录激活因子4(STAT4)不稳定,并损害2型糖尿病患者的抗病毒辅助性T细胞1(Th1)反应。
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Amino acid is a major carbon source for hepatic lipogenesis.
自闭症谱系障碍中的氧化应激与抗氧化治疗:生物化学及构效关系视角
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Different Forms of Regulated Cell Death in Type-2-Diabetes-Mellitus-Related Osteoporosis: A Focus on Mechanisms and Therapeutic Strategies.2型糖尿病相关骨质疏松症中不同形式的程序性细胞死亡:聚焦机制与治疗策略
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氨基酸是肝内脂肪生成的主要碳源。
Cell Metab. 2024 Nov 5;36(11):2437-2448.e8. doi: 10.1016/j.cmet.2024.10.001. Epub 2024 Oct 25.
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Inhibition of KDM4A restricts SQLE transcription and induces oxidative stress imbalance to suppress bladder cancer.抑制 KDM4A 会限制 SQLE 的转录并诱导氧化应激失衡,从而抑制膀胱癌。
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Malic enzymes in cancer: Regulatory mechanisms, functions, and therapeutic implications.苹果酸酶在癌症中的作用:调控机制、功能及治疗意义。
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Iron mobilization from intact ferritin: effect of differential redox activity of quinone derivatives with NADH/O and in situ-generated ROS.从完整的铁蛋白中动员铁:具有 NADH/O 差向氧化还原活性的醌衍生物和原位生成的 ROS 的影响。
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AMPK activation eliminates senescent cells in diabetic wound by inducing NCOA4 mediated ferritinophagy.AMPK 激活通过诱导 NCOA4 介导的铁蛋白自噬消除糖尿病伤口中的衰老细胞。
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Fatty acid oxidation drives mitochondrial hydrogen peroxide production by α-ketoglutarate dehydrogenase.脂肪酸氧化通过α-酮戊二酸脱氢酶驱动线粒体过氧化氢的产生。
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