单位:[1]Division of Cardiothoracic and Vascular Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China华中科技大学同济医学院附属同济医院心脏大血管外科胸外科外科学系外科学系[2]Key Laboratory of Organ Transplantation, Ministry of Education, Wuhan 430030, China[3]NHC Key Laboratory of Organ Transplantation, Wuhan 430030, China[4]Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan 430030, China[5]Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Ferroptosis was first coined in 2012 to describe the form of regulated cell death (RCD) characterized by iron-dependent lipid peroxidation. To date, ferroptosis has been implicated in many diseases, such as carcinogenesis, degenerative diseases (e.g., Huntington's, Alzheimer's, and Parkinson's diseases), ischemia-reperfusion injury, and cardiovascular diseases. Previous studies have identified numerous targets involved in ferroptosis; for example, acyl-CoA synthetase long-chain family member 4 (ACSL4) and p53 induce while glutathione peroxidase 4 (GPX4) and apoptosis-inducing factor mitochondria-associated 2 (AIFM2, also known as FSP1) inhibit ferroptosis. At least three major pathways (the glutathione-GPX4, FSP1-coenzyme Q(10) (CoQ(10)), and GTP cyclohydrolase-1- (GCH1-) tetrahydrobiopterin (BH4) pathways) have been identified to participate in ferroptosis regulation. Recent advances have also highlighted the crucial roles of posttranslational modifications (PTMs) of proteins in ferroptosis. Here, we summarize the recently discovered knowledge regarding the mechanisms underlying ferroptosis, particularly the roles of PTMs in ferroptosis regulation.
基金:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81974013, 81700249, 81873458, 81873456]; Hubei Province health and family planning scientific research project [WJ2019Q043]
第一作者单位:[1]Division of Cardiothoracic and Vascular Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China[2]Key Laboratory of Organ Transplantation, Ministry of Education, Wuhan 430030, China[3]NHC Key Laboratory of Organ Transplantation, Wuhan 430030, China[4]Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan 430030, China
共同第一作者:
通讯作者:
通讯机构:[1]Division of Cardiothoracic and Vascular Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China[2]Key Laboratory of Organ Transplantation, Ministry of Education, Wuhan 430030, China[3]NHC Key Laboratory of Organ Transplantation, Wuhan 430030, China[4]Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan 430030, China
推荐引用方式(GB/T 7714):
Wei Xiang,Yi Xin,Zhu Xue-Hai,et al.Posttranslational Modifications in Ferroptosis[J].OXIDATIVE MEDICINE AND CELLULAR LONGEVITY.2020,2020:doi:10.1155/2020/8832043.
APA:
Wei, Xiang,Yi, Xin,Zhu, Xue-Hai&Jiang, Ding-Sheng.(2020).Posttranslational Modifications in Ferroptosis.OXIDATIVE MEDICINE AND CELLULAR LONGEVITY,2020,
MLA:
Wei, Xiang,et al."Posttranslational Modifications in Ferroptosis".OXIDATIVE MEDICINE AND CELLULAR LONGEVITY 2020.(2020)