Literature DB >> 28275246

Sarcoplasmic reticulum-mitochondria communication in cardiovascular pathophysiology.

Camila Lopez-Crisosto1, Christian Pennanen1, Cesar Vasquez-Trincado1, Pablo E Morales1, Roberto Bravo-Sagua1,2, Andrew F G Quest1,3, Mario Chiong1, Sergio Lavandero1,3,4.   

Abstract

Repetitive, calcium-mediated contractile activity renders cardiomyocytes critically dependent on a sustained energy supply and adequate calcium buffering, both of which are provided by mitochondria. Moreover, in vascular smooth muscle cells, mitochondrial metabolism modulates cell growth and proliferation, whereas cytosolic calcium levels regulate the arterial vascular tone. Physical and functional communication between mitochondria and sarco/endoplasmic reticulum and balanced mitochondrial dynamics seem to have a critical role for optimal calcium transfer to mitochondria, which is crucial in calcium homeostasis and mitochondrial metabolism in both types of muscle cells. Moreover, mitochondrial dysfunction has been associated with myocardial damage and dysregulation of vascular smooth muscle proliferation. Therefore, sarco/endoplasmic reticulum-mitochondria coupling and mitochondrial dynamics are now viewed as relevant factors in the pathogenesis of cardiac and vascular diseases, including coronary artery disease, heart failure, and pulmonary arterial hypertension. In this Review, we summarize the evidence related to the role of sarco/endoplasmic reticulum-mitochondria communication in cardiac and vascular muscle physiology, with a focus on how perturbations contribute to the pathogenesis of cardiovascular disorders.

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Year:  2017        PMID: 28275246     DOI: 10.1038/nrcardio.2017.23

Source DB:  PubMed          Journal:  Nat Rev Cardiol        ISSN: 1759-5002            Impact factor:   32.419


  219 in total

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Journal:  Circ Res       Date:  2012-04-17       Impact factor: 17.367

5.  Role of the calcium-sensing receptor in cardiomyocyte apoptosis via the sarcoplasmic reticulum and mitochondrial death pathway in cardiac hypertrophy and heart failure.

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6.  Filamin depletion blocks endoplasmic spreading and destabilizes force-bearing adhesions.

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

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9.  mTORC1 inhibitor rapamycin and ER stressor tunicamycin induce differential patterns of ER-mitochondria coupling.

Authors:  Roberto Bravo-Sagua; Camila López-Crisosto; Valentina Parra; Marcelo Rodriguez-Peña; Beverly A Rothermel; Andrew F G Quest; Sergio Lavandero
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  43 in total

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Authors:  Amaneh Mohammadi Roushandeh; Yoshikazu Kuwahara; Mehryar Habibi Roudkenar
Journal:  Cytotechnology       Date:  2019-01-31       Impact factor: 2.058

Review 3.  Regulation of mitochondrial bioenergetics by the non-canonical roles of mitochondrial dynamics proteins in the heart.

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Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2017-09-14       Impact factor: 5.187

Review 4.  Is Mitochondrial Dysfunction a Common Root of Noncommunicable Chronic Diseases?

Authors:  Alexis Diaz-Vegas; Pablo Sanchez-Aguilera; James R Krycer; Pablo E Morales; Matías Monsalves-Alvarez; Mariana Cifuentes; Beverly A Rothermel; Sergio Lavandero
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Review 5.  Targeting mitochondria for cardiovascular disorders: therapeutic potential and obstacles.

Authors:  Massimo Bonora; Mariusz R Wieckowski; David A Sinclair; Guido Kroemer; Paolo Pinton; Lorenzo Galluzzi
Journal:  Nat Rev Cardiol       Date:  2019-01       Impact factor: 32.419

6.  Heart failure-induced activation of phospholipase iPLA2γ generates hydroxyeicosatetraenoic acids opening the mitochondrial permeability transition pore.

Authors:  Sung Ho Moon; Xinping Liu; Ari M Cedars; Kui Yang; Michael A Kiebish; Susan M Joseph; John Kelley; Christopher M Jenkins; Richard W Gross
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7.  In silico simulation of reversible and irreversible swelling of mitochondria: The role of membrane rigidity.

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Review 10.  MiRNAs, lncRNAs, and circular RNAs as mediators in hypertension-related vascular smooth muscle cell dysfunction.

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