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Oestradiol-mediated ferroptosis defense shapes sex differences in acute kidney injury.

作者信息

Wu Shengrong, Zhuang Li, Gan Boyi

机构信息

Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

The University of Texas MD Anderson UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.

出版信息

Cell Death Differ. 2025 Aug 28. doi: 10.1038/s41418-025-01573-w.

DOI:10.1038/s41418-025-01573-w
PMID:40877408
Abstract
摘要

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Oestradiol-mediated ferroptosis defense shapes sex differences in acute kidney injury.雌二醇介导的铁死亡防御形成急性肾损伤中的性别差异。
Cell Death Differ. 2025 Aug 28. doi: 10.1038/s41418-025-01573-w.
2
Mitochondria-mediated ferroptosis induced by CARD9 ablation prevents MDSCs-dependent antifungal immunity.CARD9 缺失诱导的线粒体介导的铁死亡可防止 MDSCs 依赖的抗真菌免疫。
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Multiple oestradiol functions inhibit ferroptosis and acute kidney injury.多种雌二醇功能可抑制铁死亡和急性肾损伤。
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Kidney hepcidin protects the collecting duct against ferroptosis in ischemia/reperfusion-induced acute kidney injury.
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Hesperetin attenuates ischemia/reperfusion-induced acute kidney injury by regulating ferroptosis in mice.橙皮素通过调节小鼠铁死亡减轻缺血/再灌注诱导的急性肾损伤。
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FBXW7-Mediated Downregulation of GPX4 Aggravates Acute Kidney Injury Following Ischemia‒Reperfusion.FBXW7介导的GPX4下调加重缺血再灌注后的急性肾损伤。
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Pharmacological inhibition of STING-mediated GPX4 autophagic degradation by 4-octyl itaconate ameliorates sepsis-induced acute kidney injury.衣康酸辛酯对STING介导的GPX4自噬降解的药理学抑制作用可改善脓毒症诱导的急性肾损伤。
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本文引用的文献

1
The roles of ferroptosis in cancer: Tumor suppression, tumor microenvironment, and therapeutic interventions.铁死亡在癌症中的作用:肿瘤抑制、肿瘤微环境和治疗干预。
Cancer Cell. 2024 Apr 8;42(4):513-534. doi: 10.1016/j.ccell.2024.03.011.
2
Differences in the epidemiology, management and outcomes of kidney disease in men and women.男性和女性肾脏病的流行病学、治疗和结局的差异。
Nat Rev Nephrol. 2024 Jan;20(1):7-20. doi: 10.1038/s41581-023-00784-z. Epub 2023 Nov 20.
3
Ferroptosis surveillance independent of GPX4 and differentially regulated by sex hormones.
铁死亡监测不依赖于 GPX4 且受性激素差异调控。
Cell. 2023 Jun 22;186(13):2748-2764.e22. doi: 10.1016/j.cell.2023.05.003. Epub 2023 Jun 1.
4
Sex differences in resilience to ferroptosis underlie sexual dimorphism in kidney injury and repair.性别在铁死亡抗性方面的差异是肾脏损伤和修复中性别二态性的基础。
Cell Rep. 2022 Nov 8;41(6):111610. doi: 10.1016/j.celrep.2022.111610.
5
Hydropersulfides Inhibit Lipid Peroxidation and Protect Cells from Ferroptosis.巯基化合物抑制脂质过氧化并保护细胞免受铁死亡。
J Am Chem Soc. 2022 Aug 31;144(34):15825-15837. doi: 10.1021/jacs.2c06804. Epub 2022 Aug 17.
6
Ferroptosis turns 10: Emerging mechanisms, physiological functions, and therapeutic applications.铁死亡研究十周年:新兴机制、生理功能与治疗应用
Cell. 2022 Jul 7;185(14):2401-2421. doi: 10.1016/j.cell.2022.06.003.
7
Plasticity of ether lipids promotes ferroptosis susceptibility and evasion.醚脂的可塑性促进了铁死亡易感性和逃逸。
Nature. 2020 Sep;585(7826):603-608. doi: 10.1038/s41586-020-2732-8. Epub 2020 Sep 16.
8
The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis.辅酶 Q 氧化还原酶 FSP1 与 GPX4 平行作用以抑制铁死亡。
Nature. 2019 Nov;575(7784):688-692. doi: 10.1038/s41586-019-1705-2. Epub 2019 Oct 21.
9
FSP1 is a glutathione-independent ferroptosis suppressor.FSP1 是一种谷胱甘肽不依赖的铁死亡抑制因子。
Nature. 2019 Nov;575(7784):693-698. doi: 10.1038/s41586-019-1707-0. Epub 2019 Oct 21.
10
Synchronized renal tubular cell death involves ferroptosis.同步性肾小管细胞死亡涉及铁死亡。
Proc Natl Acad Sci U S A. 2014 Nov 25;111(47):16836-41. doi: 10.1073/pnas.1415518111. Epub 2014 Nov 10.