Ferroptosis: Opportunities and Challenges in Myocardial Ischemia-Reperfusion Injury

被引:123
作者
Zhao W.-K. [1 ]
Zhou Y. [2 ,3 ]
Xu T.-T. [1 ]
Wu Q. [4 ]
机构
[1] Department of Health Care Ward, First Affiliated Hospital of Guilin Medical University, Guangxi Zhuang Autonomous Region, Guilin
[2] Department of Pathophysiology, Xuzhou Medical University, Jiangsu province, Xuzhou
[3] Laboratory of Clinical and Experimental Pathology, Xuzhou Medical University, Jiangsu province, Xuzhou
[4] Department of Physiology, Xuzhou Medical University, Jiangsu province, Xuzhou
基金
中国国家自然科学基金;
关键词
Oxidative stress - Lipids - Oxidation;
D O I
10.1155/2021/9929687
中图分类号
学科分类号
摘要
Ferroptosis is a newly discovered form of regulated cell death dependent on iron and reactive oxygen species (ROS). It directly or indirectly affects the activity of glutathione peroxidases (GPXs) under the induction of small molecules, causing membrane lipid peroxidation due to redox imbalances and excessive ROS accumulation, damaging the integrity of cell membranes. Ferroptosis is mainly characterized by mitochondrial shrinkage, increased density of bilayer membranes, and the accumulation of lipid peroxidation. Myocardial ischemia-reperfusion injury (MIRI) is an unavoidable risk event for acute myocardial infarction. Ferroptosis is closely associated with MIRI, and this relationship is discussed in detail here. This review systematically summarizes the process of ferroptosis and the latest research progress on the role of ferroptosis in MIRI to provide new ideas for the prevention and treatment of MIRI. © 2021 Wei-kun Zhao et al.
引用
收藏
相关论文
共 99 条
[81]  
Hannenhalli S., Kaestner K.H., The evolution of fox genes and their role in development and disease, Nature Reviews. Genetics, 10, 4, pp. 233-240, (2009)
[82]  
Fan Z., Cai L., Wang S., Wang J., Chen B., Baicalin prevents myocardial ischemia/reperfusion injury through inhibiting ACSL4 mediated ferroptosis, Frontiers in Pharmacology, 12, (2021)
[83]  
Chan W., Taylor A.J., Ellims A.H., Lefkovits L., Wong C., Kingwell B.A., Natoli A., Croft K.D., Mori T., Kaye D.M., Dart A.M., Duffy S.J., Effect of iron chelation on myocardial infarct size and oxidative stress in ST-elevation-myocardial infarction, Circulation. Cardiovascular Interventions, 5, 2, pp. 270-278, (2012)
[84]  
Stamenkovic A., O'Hara K.A., Nelson D.C., Maddaford T.G., Edel A.L., Maddaford G., Dibrov E., Aghanoori M.R., Kirshenbaum L.A., Fernyhough P., Aliani M., Pierce G.N., Ravandi A., Oxidized phosphatidylcholines trigger ferroptosis in cardiomyocytes during ischemia-reperfusion injury, American Journal of Physiology. Heart and Circulatory Physiology, 320, 3, pp. H1170-H1184, (2021)
[85]  
Shan X., Lv Z.Y., Yin M.J., Chen J., Wang J., Wu Q.N., The Protective Effect of Cyanidin-3-Glucoside on Myocardial Ischemia- Reperfusion Injury through Ferroptosis, Oxidative Medicine and Cellular Longevity, 2021, (2021)
[86]  
Wang C.Y., Zhu L.J., Yuan W.L., Sun L., Xia Z., Zhang Z., Yao W., Diabetes aggravates myocardial ischaemia reperfusion injury via activating Nox2-related programmed cell death in an AMPK-dependent manner, Journal of Cellular and Molecular Medicine, 24, 12, pp. 6670-6679, (2020)
[87]  
Li W.G., Feng G.S., Gauthier J.M., Lokshina I., Higashikubo R., Evans S., Liu X., Hassan A., Tanaka S., Cicka M., Hsiao H.M., Ruiz-Perez D., Bredemeyer A., Gross R.W., Mann D.L., Tyurina Y.Y., Gelman A.E., Kagan V.E., Linkermann A., Lavine K.J., Kreisel D., Ferroptotic cell death and TLR4/Trif signaling initiate neutrophil recruitment after heart transplantation, The Journal of Clinical Investigation, 129, 6, pp. 2293-2304, (2019)
[88]  
Yang W.S., SriRamaratnam R., Welsch M.E., Shimada K., Skouta R., Viswanathan V.S., Cheah J.H., Clemons P.A., Shamji A.F., Clish C.B., Brown L.M., Girotti A.W., Cornish V.W., Schreiber S.L., Stockwell B.R., Regulation of ferroptotic cancer cell death by GPX4, Cell, 156, 1-2, pp. 317-331, (2014)
[89]  
Dixon S.J., Winter G.E., Musavi L.S., Lee E.D., Snijder B., Rebsamen M., Superti-Furga G., Stockwell B.R., Human haploid cell genetics reveals roles for lipid metabolism genes in nonapoptotic cell death, Acs Chemical Biology, 10, 7, pp. 1604-1609, (2015)
[90]  
Lorincz T., Jemnitz K., Kardon T., Mandl J., Szarka A., Ferroptosis is involved in acetaminophen induced cell death, Pathology & Oncology Research, 21, 4, pp. 1115-1121, (2015)