铁蛋白沉积：急性肺损伤的潜在靶点

IF 4.8 3区医学 Q2 CELL BIOLOGY

Inflammation Research Pub Date : 2024-10-01 Epub Date: 2024-08-17 DOI:10.1007/s00011-024-01919-z

Yuqi Wen, Yang Liu, Weihong Liu, Wenli Liu, Jinyan Dong, Qingkuo Liu, Zhen Yu, Hongsheng Ren, Hao Hao

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引用次数: 0

摘要

急性肺损伤（ALI）由多种肺内和肺外因素引起，发病率和死亡率都很高。氧化应激是急性肺损伤病理机制的重要组成部分。铁氧化是一种有别于其他细胞死亡的程序性细胞死亡模式，其特点是铁依赖性脂质过氧化。本文综述了铁变态反应的代谢调控、铁变态反应在 ALI 发病机制中的作用，以及将铁变态反应作为 ALI 药物治疗的靶点。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Ferroptosis: a potential target for acute lung injury.

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Ferroptosis: a potential target for acute lung injury.

Acute lung injury (ALI) is caused by a variety of intrapulmonary and extrapulmonary factors and is associated with high morbidity and mortality. Oxidative stress is an important part of the pathological mechanism of ALI. Ferroptosis is a mode of programmed cell death distinguished from others and characterized by iron-dependent lipid peroxidation. This article reviews the metabolic regulation of ferroptosis, its role in the pathogenesis of ALI, and the use of ferroptosis as a therapeutic target regarding the pharmacological treatment of ALI.

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来源期刊

Inflammation Research 医学-免疫学

CiteScore

9.90

自引率

1.50%

发文量

134

审稿时长

3-8 weeks

期刊介绍： Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.