Ferritinophagy and ferroptosis in the management of metabolic diseases

被引:246
作者
Ajoolabady, Amir [1 ]
Aslkhodapasandhokmabad, Hami [2 ]
Libby, Peter [3 ]
Tuomeilehto, Jaakko [4 ,5 ,6 ]
Lip, Gregory Y. H. [7 ]
Penninger, Josef M. [8 ,9 ]
Richarrdson, Des. R. [10 ,11 ,12 ,13 ]
Tang, Daoli [14 ]
Zhou, Hao [1 ,15 ]
Wang, Shuyi [1 ,16 ]
Kionsky, Daniel . J. [17 ,18 ]
Kroemer, Guido [19 ,20 ,21 ,22 ,23 ]
Ren, Jun [24 ,25 ]
机构
[1] Univ Wyoming, Coll Hlth Sci, Ctr Cardiovasc Res & Alternat Med, Laramie, WY 82071 USA
[2] Univ Visayas, Gullas Coll Med, Dionisio Jakosalem St, Cebu 6000, Cebu, Philippines
[3] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Cardiovasc Med, Boston, MA 02115 USA
[4] Finnish Inst Hlth & Welf, Publ Hlth Promot Unit, Helsinki, Finland
[5] Univ Helsinki, Dept Publ Hlth, Helsinki, Finland
[6] King Abdulaziz Univ, Diabet Res Grp, Jeddah, Saudi Arabia
[7] Univ Liverpool, Inst Ageing & Chron Dis, Liverpool Ctr Cardiovasc Sci, Liverpool, Merseyside, England
[8] Austrian Acad Sci IMBA, Inst Mol Biotechnol, Vienna Bioctr VBC, Vienna, Austria
[9] Univ British Columbia, Life Sci Inst, Dept Med Genet, Vancouver, BC, Canada
[10] Univ Sydney, Mol Pharmacol & Pathol Program, Dept Pathol, Med Fdn Bldg K25, Sydney, NSW 2006, Australia
[11] Univ Sydney, Bosch Inst, Med Fdn Bldg K25, Sydney, NSW 2006, Australia
[12] Nagoya Univ, Dept Pathol & Biol Responses, Grad Sch Med, Nagoya, Aichi 4668550, Japan
[13] Griffith Univ, Griffith Inst Drug Discovery, Ctr Canc Cell Biol & Drug Discovery, Brisbane, Qld 4111, Australia
[14] UT Southwestern Med Ctr, Dept Surg, Dallas, TX 75390 USA
[15] Chinese Peoples Liberat Army Gen Hosp, Med Sch Chinese PLA, Beijing 100853, Peoples R China
[16] Shanghai Univ, Sch Med, Shanghai 200444, Peoples R China
[17] Univ Michigan, Life Sci Inst, Ann Arbor, MI 48109 USA
[18] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[19] Univ Paris, Ctr Rech Cordeliers, Equipe Labellisee Ligue Canc, Sorbonne Univ,INSERM,U1138,Inst Univ France, Paris, France
[20] Inst Gustave Roussy, Metabol & Cell Biol Platforms, Villejuif, France
[21] Hop Europeen Georges Pompidou, AP HP, Pole Biol, Paris, France
[22] Chinese Acad Med Sci, Suzhou Inst Syst Med, Suzhou, Peoples R China
[23] Karolinska Inst, Karolinska Univ Hosp, Dept Womens & Childrens Hlth, Stockholm, Sweden
[24] Fudan Univ, Shanghai Inst Cardiovasc Dis, Dept Cardiol, Zhongshan Hosp, Shanghai 200032, Peoples R China
[25] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98195 USA
关键词
ISCHEMIA-REPERFUSION; PROMOTES FERROPTOSIS; MEDIATES FERROPTOSIS; AUTOPHAGY INHIBITOR; LIPID-PEROXIDATION; NEURONAL DEATH; IN-VIVO; IRON; ACTIVATION; INJURY;
D O I
10.1016/j.tem.2021.04.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ferroptosis is a form of regulated cell death modality associated with disturbed iron-homeostasis and unrestricted lipid peroxidation. Ample evidence has depicted an essential role for ferroptosis as either the cause or consequence for human diseases, denoting the likely therapeutic promises for targeting ferroptosis in the preservation of human health. Ferritinophagy, a selective form of autophagy, contributes to the initiation of ferroptosis through degradation of ferritin, which triggers labile iron overload (IO), lipid peroxidation, membrane damage, and cell death. In this review, we will delineate the role of ferritinophagy in ferroptosis, and its underlying regulatory mechanisms, to unveil the therapeutic value of ferritinophagy as a target in the combat of ferroptosis to manage metabolic diseases.
引用
收藏
页码:444 / 462
页数:19
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