Doll Sebastian, Conrad Marcus
Helmholtz Zentrum München, Institute of Developmental Genetics, Neuherberg, Germany.
IUBMB Life. 2017 Jun;69(6):423-434. doi: 10.1002/iub.1616. Epub 2017 Mar 9.
Ferroptosis is a recently described form of regulated necrotic cell death, which appears to contribute to a number of diseases, such as tissue ischemia/reperfusion injury, acute renal failure, and neurodegeneration. A hallmark of ferroptosis is iron-dependent lipid peroxidation, which can be inhibited by the key ferroptosis regulator glutathione peroxidase 4(Gpx4), radical trapping antioxidants and ferroptosis-specific inhibitors, such as ferrostatins and liproxstatins, as well as iron chelation. Although great strides have been made towards a better understanding of the proximate signals of distinctive lipid peroxides in ferroptosis, still little is known about the mechanistic implication of iron in the ferroptotic process. Hence, this review aims at summarizing recent advances in our understanding to what is known about enzymatic and nonenzymatic routes of lipid peroxidation, the involvement of iron in this process and the identification of novel players in ferroptotic cell death. Additionally, we review early works carried out long time before the term "ferroptosis" was actually introduced but which were instrumental in a better understanding of the role of ferroptosis in physiological and pathophysiological contexts. © 2017 IUBMB Life, 69(6):423-434, 2017.
铁死亡是一种最近被描述的受调控的坏死性细胞死亡形式,它似乎与多种疾病有关,如组织缺血/再灌注损伤、急性肾衰竭和神经退行性变。铁死亡的一个标志是铁依赖性脂质过氧化,它可以被关键的铁死亡调节因子谷胱甘肽过氧化物酶4(Gpx4)、自由基捕获抗氧化剂和铁死亡特异性抑制剂(如铁抑素和脂氧素他汀)以及铁螯合作用所抑制。尽管在更好地理解铁死亡中独特脂质过氧化物的近端信号方面已经取得了很大进展,但对于铁在铁死亡过程中的机制意义仍然知之甚少。因此,本综述旨在总结我们在理解脂质过氧化的酶促和非酶促途径、铁在这一过程中的作用以及铁死亡细胞死亡中新型参与者的鉴定方面的最新进展。此外,我们还回顾了在“铁死亡”一词实际提出之前很久就进行的早期研究,这些研究有助于更好地理解铁死亡在生理和病理生理背景中的作用。© 2017国际生物化学与分子生物学联盟生命科学,69(6):423 - 434,2017。