OPA1 in Cardiovascular Health and Disease

被引:18
|
作者
Burke, Niall [1 ]
Hall, Andrew R. [1 ]
Hausenloy, Derek J. [1 ,2 ,3 ]
机构
[1] UCL, Hatter Cardiovasc Inst, 67 Chenies Mews, London WC1E 6HX, England
[2] Duke NUS Grad Med Sch, Cardiovasc & Metab Disorders Program, Singapore, Singapore
[3] Natl Heart Ctr, Natl Heart Res Inst Singapore, Singapore, Singapore
基金
英国医学研究理事会;
关键词
Cardiovascular disease; fission; fusion; mitochondrial morphology; OPA1; DOMINANT OPTIC ATROPHY; CYTOCHROME-C RELEASE; MITOCHONDRIAL PROTEASE OMA1; DYNAMIN-RELATED PROTEIN; PROTEOLYTIC CLEAVAGE; OXIDATIVE-PHOSPHORYLATION; RESPIRATORY-CHAIN; GTPASE OPA1; FUSION; MORPHOLOGY;
D O I
10.2174/1389450116666150102113648
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mitochondria are known to play crucial roles in normal cellular physiology and in more recent years they have been implicated in a wide range of pathologies. Central to both these roles is their ability to alter their shape interchangeably between two different morphologies: an elongated interconnected network and a fragmented discrete phenotype - processes which are under the regulation of the mitochondrial fusion and fission proteins, respectively. In this review article, we focus on the mitochondrial fusion protein optic atrophy protein 1 (OPA1) in cardiovascular health and disease and we explore its role as a potential therapeutic target for treating cardiovascular and metabolic disease.
引用
收藏
页码:912 / 920
页数:9
相关论文
共 50 条
  • [31] Mitochondrial retention of Opa1 is required for mouse embryogenesis
    Moore, Billie A.
    Aviles, Gladys D. Gonzalez
    Larkins, Christine E.
    Hillman, Michael J.
    Caspary, Tamara
    MAMMALIAN GENOME, 2010, 21 (7-8) : 350 - 360
  • [32] Consequences and adaptations to OPA1 deficiency in the mouse liver
    Ludwig, K. Aguilar
    Barros, S. Costa
    Vanasco, V.
    Sebastian, D.
    Hernandez-Alvarez, M.
    Zorzano, A.
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2024, 54
  • [33] OPA1, the disease gene for optic atrophy type Kjer, is expressed in the inner ear
    Stefanie Bette
    Ulrike Zimmermann
    Bernd Wissinger
    Marlies Knipper
    Histochemistry and Cell Biology, 2007, 128 : 421 - 430
  • [34] Tau phosphorylation and OPA1 proteolysis are unrelated events: Implications for Alzheimer's Disease
    Alavi, Marcel, V
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2021, 1868 (12):
  • [35] The Balance of MFN2 and OPA1 in Mitochondrial Dynamics, Cellular Homeostasis, and Disease
    Zanfardino, Paola
    Amati, Alessandro
    Perrone, Mirko
    Petruzzella, Vittoria
    BIOMOLECULES, 2025, 15 (03)
  • [36] Optic neuropathy -: The OPA1 gene and optic neuropathy
    Alward, WLM
    BRITISH JOURNAL OF OPHTHALMOLOGY, 2003, 87 (01) : 2 - 3
  • [37] OPA1 affects lipid metabolism and atherosclerosis progression
    Da Dalt, L.
    Moregola, A.
    Svecla, M.
    Pedretti, S.
    Fantini, F.
    Donetti, E.
    Mitro, N.
    Scorrano, L.
    Norata, G. D.
    CARDIOVASCULAR RESEARCH, 2024, 120
  • [38] OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions
    Del Dotto, Valentina
    Mishra, Prashant
    Vidoni, Sara
    Fogazza, Mario
    Maresca, Alessandra
    Caporali, Leonardo
    McCaffery, J. Michael
    Cappelletti, Martina
    Baruffini, Enrico
    Lenaers, Guy
    Chan, David
    Rugolo, Michela
    Carelli, Valerio
    Zanna, Claudia
    CELL REPORTS, 2017, 19 (12): : 2557 - 2571
  • [39] OPA1 and cardiolipin team up for mitochondrial fusion
    Liu, Raymond
    Chan, David C.
    NATURE CELL BIOLOGY, 2017, 19 (07) : 760 - 762
  • [40] First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation
    Kamakari, Smaragda
    Koutsodontis, George
    Tsilimbaris, Miltiadis
    Fitsios, Athanasios
    Chrousos, Georgia
    MOLECULAR VISION, 2014, 20 : 691 - 703