缺氧和铁蛋白沉积

IF 4.4 2区 生物学 Q2 CELL BIOLOGY
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引用次数: 0

摘要

铁中毒是一种新型的铁依赖性细胞死亡,其特点是铁中毒脂质过氧化物过度积累,最终导致细胞膜氧化损伤。铁、脂质、氨基酸代谢和其他信号通路都控制着铁变态反应。在正常和病理情况下,许多身体组织都会出现缺氧。组织细胞可通过激活缺氧诱导因子(HIF)信号通路和其他机制来适应这些变化,以应对缺氧环境。近年来,越来越多的证据表明,缺氧与铁蛋白沉积密切相关,缺氧可通过不同途径调控特定细胞和条件下的铁蛋白沉积。本文综述了缺氧诱导因子可能对铁氧化的正负调控机制,以及与铁氧化相关的缺血性疾病,旨在为防御和治疗与铁氧化相关的缺氧性疾病提供新的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxia and ferroptosis

Ferroptosis is a novel, iron-dependent cell death characterized by the excessive accumulation of ferroptosis lipid peroxides ultimately leading to oxidative damage to the cell membrane. Iron, lipid, amino acid metabolism, and other signaling pathways all control ferroptosis. Numerous bodily tissues experience hypoxia under normal and pathological circumstances. Tissue cells can adjust to these changes by activating the hypoxia-inducible factor (HIF) signaling pathway and other mechanisms in response to the hypoxic environment. In recent years, there has been increasing evidence that hypoxia and ferroptosis are closely linked, and that hypoxia can regulate ferroptosis in specific cells and conditions through different pathways. In this paper, we review the possible positive and negative regulatory mechanisms of ferroptosis by hypoxia-inducible factors, as well as ferroptosis-associated ischemic diseases, with the intention of delivering novel therapeutic avenues for the defense and management of hypoxic illnesses linked to ferroptosis.

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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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