Literature DB >> 22793879

Mitochondrial dynamics in cardiovascular health and disease.

Sang-Bing Ong1, Andrew R Hall, Derek J Hausenloy.   

Abstract

SIGNIFICANCE: Mitochondria are dynamic organelles capable of changing their shape and distribution by undergoing either fission or fusion. Changes in mitochondrial dynamics, which is under the control of specific mitochondrial fission and fusion proteins, have been implicated in cell division, embryonic development, apoptosis, autophagy, and metabolism. Although the machinery for modulating mitochondrial dynamics is present in the cardiovascular system, its function there has only recently been investigated. In this article, we review the emerging role of mitochondrial dynamics in cardiovascular health and disease. RECENT ADVANCES: Changes in mitochondrial dynamics have been implicated in vascular smooth cell proliferation, cardiac development and differentiation, cardiomyocyte hypertrophy, myocardial ischemia-reperfusion injury, cardioprotection, and heart failure. CRITICAL ISSUES: Many of the experimental studies investigating mitochondrial dynamics in the cardiovascular system have been confined to cardiac cell lines, vascular cells, or neonatal cardiomyocytes, in which mitochondria are distributed throughout the cytoplasm and are free to move. However, in the adult heart where mitochondrial movements are restricted by their tightly-packed distribution along myofibrils or beneath the subsarcolemma, the relevance of mitochondrial dynamics is less obvious. The investigation of transgenic mice deficient in cardiac mitochondrial fission or fusion proteins should help elucidate the role of mitochondrial dynamics in the adult heart. FUTURE DIRECTIONS: Investigating the role of mitochondrial dynamics in cardiovascular health and disease should result in the identification of novel therapeutic targets for treating patients with cardiovascular disease, the leading cause of death and disability globally.

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Year:  2012        PMID: 22793879      PMCID: PMC3699895          DOI: 10.1089/ars.2012.4777

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  114 in total

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2.  Mitofusins are required for angiogenic function and modulate different signaling pathways in cultured endothelial cells.

Authors:  Jesse J Lugus; Gladys A Ngoh; Markus M Bachschmid; Kenneth Walsh
Journal:  J Mol Cell Cardiol       Date:  2011-08-02       Impact factor: 5.000

3.  Mutation of the protein kinase A phosphorylation site influences the anti-proliferative activity of mitofusin 2.

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5.  Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.

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Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-19       Impact factor: 11.205

7.  Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.

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Journal:  Am J Pathol       Date:  1998-11       Impact factor: 4.307

8.  Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells.

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Journal:  J Cell Biol       Date:  2010-12-13       Impact factor: 10.539

9.  Human MIEF1 recruits Drp1 to mitochondrial outer membranes and promotes mitochondrial fusion rather than fission.

Authors:  Jian Zhao; Tong Liu; Shaobo Jin; Xinming Wang; Mingqi Qu; Per Uhlén; Nikolay Tomilin; Oleg Shupliakov; Urban Lendahl; Monica Nistér
Journal:  EMBO J       Date:  2011-06-24       Impact factor: 11.598

10.  The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice.

Authors:  Junko Wakabayashi; Zhongyan Zhang; Nobunao Wakabayashi; Yasushi Tamura; Masahiro Fukaya; Thomas W Kensler; Miho Iijima; Hiromi Sesaki
Journal:  J Cell Biol       Date:  2009-09-14       Impact factor: 10.539

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  82 in total

Review 1.  Maturing human pluripotent stem cell-derived cardiomyocytes in human engineered cardiac tissues.

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Review 2.  Mechanisms of exercise-induced cardioprotection.

Authors:  Scott K Powers; Ashley J Smuder; Andreas N Kavazis; John C Quindry
Journal:  Physiology (Bethesda)       Date:  2014-01

Review 3.  Mitochondrial reactive oxygen species at the heart of the matter: new therapeutic approaches for cardiovascular diseases.

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Journal:  Circ Res       Date:  2015-05-22       Impact factor: 17.367

Review 4.  Exercise: Teaching myocytes new tricks.

Authors:  Scott K Powers
Journal:  J Appl Physiol (1985)       Date:  2017-06-01

5.  The first direct activity assay for the mitochondrial protease OMA1.

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Journal:  Mitochondrion       Date:  2019-03-26       Impact factor: 4.160

Review 6.  Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment.

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Journal:  Mol Syndromol       Date:  2016-06-03

7.  Parkin-independent mitophagy requires Drp1 and maintains the integrity of mammalian heart and brain.

Authors:  Yusuke Kageyama; Masahiko Hoshijima; Kinya Seo; Djahida Bedja; Polina Sysa-Shah; Shaida A Andrabi; Weiran Chen; Ahmet Höke; Valina L Dawson; Ted M Dawson; Kathleen Gabrielson; David A Kass; Miho Iijima; Hiromi Sesaki
Journal:  EMBO J       Date:  2014-10-27       Impact factor: 11.598

8.  Following the Dynamism of the Mitochondrial Network in T Cells.

Authors:  Arianna Di Daniele; Luca Simula; Silvia Campello
Journal:  Methods Mol Biol       Date:  2021

9.  Binding of FUN14 Domain Containing 1 With Inositol 1,4,5-Trisphosphate Receptor in Mitochondria-Associated Endoplasmic Reticulum Membranes Maintains Mitochondrial Dynamics and Function in Hearts in Vivo.

Authors:  Shengnan Wu; Qiulun Lu; Qilong Wang; Ye Ding; Zejun Ma; Xiaoxiang Mao; Kai Huang; Zhonglin Xie; Ming-Hui Zou
Journal:  Circulation       Date:  2017-09-23       Impact factor: 29.690

10.  Regulation of PP2Cm expression by miRNA-204/211 and miRNA-22 in mouse and human cells.

Authors:  Bang-fen Pan; Chen Gao; Shu-xun Ren; Yi-bin Wang; Hai-peng Sun; Mei-yi Zhou
Journal:  Acta Pharmacol Sin       Date:  2015-11-23       Impact factor: 6.150

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