OPA1 regulation of mitochondrial dynamics in skeletal and cardiac muscle

被引:48
|
作者
Noone, John [1 ,2 ,3 ,4 ]
O'Gorman, Donal J. [1 ,2 ,5 ]
Kenny, Helena C. [6 ,7 ]
机构
[1] Dublin Univ, Sch Hlth & Human Performance, Diabet Partnership 3U, Dublin, Ireland
[2] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin, Ireland
[3] Trinity Coll Dublin, Sch Biochem & Immunol, Trinity Biomed Sci Inst TBSI, Dublin, Ireland
[4] Translat Res Inst, AdventHealth, Orlando, FL USA
[5] SFI Res Ctr forPharmaceut, Bernal Inst, SSPC, Limerick, Ireland
[6] Univ Iowa, Carver Coll Med, Dept Internal Med, Div Endocrinol & Metab, Iowa City, IA USA
[7] Univ Iowa, Fraternal Order Eagles Diabet Res Ctr, Iowa, IA USA
来源
关键词
HEART-FAILURE; CELL-DEATH; FUSION; FISSION; DISEASE; DYSFUNCTION; HOMEOSTASIS; BIOGENESIS; DEFICIENCY; METABOLISM;
D O I
10.1016/j.tem.2022.07.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mitochondria are double-membrane organelles integral for energy metabolism. Mitochondrial dynamics is regulated by inner and outer mitochondrial membrane (IMM and OMM) proteins, which promote fission and fusion. Optic atrophy 1 (OPA1) regulates IMM fusion, prevents apoptosis, and is a key regulator of morphological change in skeletal and cardiac muscle physiology and pathophysiology. OPA1 fuses the inner membranes of adjacent mitochondria, allowing for an increase in oxidative phosphorylation (OXPHOS). Considering the importance of energy metabolism in whole-body physiology, OPA1 and its regulators have been proposed as novel targets for the treatment of skeletal muscle atrophy and heart failure. Here, we review the role and regulation of OPA1 in skeletal muscle and cardiac pathophysiology, epitomizing its critical role in the cell.
引用
收藏
页码:710 / 721
页数:12
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