Abstract:Iron death is a new type of iron dependent programmed cell death, which is caused by the increase of fatty acid lipid peroxidation and the accumulation of reactive oxygen species induced by cell iron overload. Iron death is closely related to the occurrence and development of many major diseases such as tumor, neurodegenerative disease, metabolic disease and aging disease. Iron death is involved in many disease processes such as cardiomyopathy, myocardial infarction, heart failure, coronary atherosclerosis, myocardial ischemia-reperfusion injury, and diabetic cardiomyopathy. In this paper, the possible mechanisms of iron death in various pathological processes of cardiovascular disease are reviewed, which will help to improve understanding of iron death in cardiovascular disease.
刘力恒 王艳滢 焦磊 张莹. 铁死亡在心血管疾病中的研究进展[J]. 中国医药导报, 2021, 18(25): 44-46,79.
LIU Liheng WANG Yanying JIAO Lei ZHANG Ying. Research progress of iron death in cardiovascular disease. 中国医药导报, 2021, 18(25): 44-46,79.
[1] 中国心血管健康与疾病报告编写组.中国心血管健康与疾病报告2019概要[J].中国循环杂志,2020,35(9):833-854.
[2] Ndrepepa G. Myeloperoxidase-A bridge linking inflammation and oxidative stress with cardiovascular disease [J]. Clin Chim Acta,2019,493:36-51.
[3] Ravingerová T,Kindernay L,Barteková M,et al. The Molecular Mechanisms of Iron Metabolism and Its Role in Cardiac Dysfunction and Cardioprotection [J]. Int J Mol Sci,2020,21(21):7889.
[4] Hirschhorn T,Stockwell BR. The development of the concept of ferroptosis [J]. Free Radic Biol Med,2019,133:130-143.
[5] Hao S,Liang B,Huang Q,et al. Metabolic networks in ferroptosis [J]. Oncol Lett,2018,15(4):5405-5411.
[6] S?觟nmez AF,Hukkaml?覦 B,Budak H. Coaction of hepatic thioredoxin and glutathione systems in iron overload-induced oxidative stress [J]. J Biochem Mol Toxicol,2021, 3:e22704.
[7] Stockwell BR,Friedmann Angeli JP,Bayir H,et al. Ferroptosis:A Regulated Cell Death Nexus Linking Metabolism,Redox Biology,and Disease [J]. Cell,2017,171(2):273-285.
[8] Feng H,Stockwell BR. Unsolved mysteries:How doeslipid peroxidation cause ferroptosis? [J]. PLoS Biol,2018,16:e2006203.
[9] Gao H,Bai Y,Jia Y,et al. Ferroptosis is a lysosomal cell death process [J]. Biochem Biophys Res Commun,2018,503(3):1550-1556.
[10] Liu Y,Sun Y,Chengping H,et al. Perivascular Adipose Tissue as an Indication,Contributor to,and Therapeutic Target for Atherosclerosis [J]. Front Physiol,2020,11:615503.
[11] Zhu Y,Zhang Y,Huang X,et al. Z-Ligustilide protects vascular endothelial cells from oxidative stress and rescues high fat diet-induced atherosclerosis by activating multiple NRF2 downstream genes [J]. Atherosclerosis,2019,284:110-120.
[12] Libby P. Inflammation in Atherosclerosis-No Longer a Theory [J]. Clin Chem,2021,67(1):131-142.
[13] Li B,Gong J,Sheng S,et al. Increased hepcidin in hemorrhagic plaques correlates with iron-stimulated IL-6/STAT3 pathway activation in macrophages [J]. Biochem Biophys Res Commun,2019,515(2):394-400.
[14] Xiao L,Luo G,Guo X,et al. Macrophage iron retention aggravates atherosclerosis:Evidence for the role of autocrine formation of hepcidin in plaque macrophages [J]. Biochim Biophys Acta Mol Cell Biol Lipids,2020,1865(2):158531.
[15] Park TJ,Park JH,Lee GS,et al. Quantitative proteomic analyses reveal that GPX4 downregulation during myocardial infarction contributes to ferroptosis in cardiomyocytes [J]. Cell Death Dis,2019,10(11):835.
[16] Song Y,Wang B,Zhu X,et al. Human umbilical cord blood-derived MSCs exosome attenuate myocardial injury by inhibiting ferroptosis in acute myocardial infarction mice [J]. Cell Biol Toxicol,2021,37(1):51-56.
[17] Tang S,WangY,Ma T,et al. MiR-30d inhibits cardiomyocytes autophagy promoting ferroptosis after myocardial infarction [J]. Panminerva Med,2020. DOI:10.23736/S0031-0808.20.03979-8.
[18] Gao M,Monian P,Quadri N,et al. Glutaminolysis and Transferrin Regulate Ferroptosis [J]. Mol Cell,2015,59(2):298-308.
[19] Zhou Y,Chen Y,Xu C,et al. TLR4 Targeting as a Promising Therapeutic Strategy for Alzheimer Disease Treatment [J]. Front Neurosci,2020,14:602508.
[20] Richard K,Perkins DJ,Harberts EM,et al. Dissociation of TRIF bias and adjuvanticity [J]. Vaccine,2020,38:4298-4308.
[21] Li W,Feng G,Gauthier JM,et al. Ferroptotic cell death and TLR4/Trif signaling initiate neutrophil recruitment after heart transplantation [J]. J Clin Invest,2019,129(6):2293-2304.
[22] Bayeva M,Khechaduri A,Puig S,et al. mTOR regulates cellular iron homeostasis through tristetraprolin [J]. Cell Metab,2012,16:645-657.
[23] Baba Y,Higa JK,Shimada BK,et al. Shimada. Protective effects of the mechanistic target of rapamycin against excess iron and ferroptosis in cardiomyocytes [J]. Am J Physiol Heart Circ Physiol,2018,314(3):H659-H668.
[24] Liu B,Zhao C,Li H,et al. Puerarin protects against heart failure induced by pressure overload through mitigation of ferroptosis [J]. Biochem Biophys Res Commun,2018, 497(1):233-240.
[25] Chen X,Xu S,Zhao C,et al. Role of TLR4/NADPH oxidase 4 pathway in promoting cell death through autophagy and ferroptosis during heart failure [J]. Biochem Biophys Res Commun,2019,516(1):37-43.
[26] Fang X,Wang H,Han D,et al. Ferroptosis as a target for protection against cardiomyopathy [J]. Proc Natl Acad Sci U S A,2019,116(7):2672-2680.
[27] Jia G,Hill M,Sowers JR. Diabetic Cardiomyopathy:An Update of Mechanisms Contributing to This Clinical Entity [J]. Circ Res,2018,122(4):624-638.
[28] Das SK,Wang W,Zhabyeyev P,et al. Iron-overload injury and cardiomyopathy in acquired and genetic models is attenuated by resveratrol therapy [J]. Sci Rep,2015,5:18132.
[29] Zou C,Liu X,Xie R,et al. Deferiprone attenuates inflammation and myocardial fibrosis in diabetic cardiomyopathy rats [J]. Biochem Biophys Res Commun,2017, 486(4):930-936.
[30] Hassannia B,Vandenabeele P,Vanden BT. Targeting Ferroptosis to Iron Out Cancer [J]. Cancer Cell,2019,35(6):830-849.
[31] Liang C,Zhang X,Yang M,et al. Recent Progress in Ferroptosis Inducers for Cancer Therapy [J]. Adv Mater,2019,31:e1904197.