Mechanotransduction and Metabolism in Cardiomyocyte Microdomains

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Mechanotransduction and Metabolism in Cardiomyocyte Microdomains

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Title: Mechanotransduction and Metabolism in Cardiomyocyte Microdomains
Author: Pasqualini, Francesco S.; Nesmith, Alexander P.; Horton, Renita E.; Sheehy, Sean P.; Parker, Kevin Kit

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Citation: Pasqualini, Francesco S., Alexander P. Nesmith, Renita E. Horton, Sean P. Sheehy, and Kevin Kit Parker. 2016. “Mechanotransduction and Metabolism in Cardiomyocyte Microdomains.” BioMed Research International 2016 (1): 4081638. doi:10.1155/2016/4081638. http://dx.doi.org/10.1155/2016/4081638.
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Abstract: Efficient contractions of the left ventricle are ensured by the continuous transfer of adenosine triphosphate (ATP) from energy production sites, the mitochondria, to energy utilization sites, such as ionic pumps and the force-generating sarcomeres. To minimize the impact of intracellular ATP trafficking, sarcomeres and mitochondria are closely packed together and in proximity with other ultrastructures involved in excitation-contraction coupling, such as t-tubules and sarcoplasmic reticulum junctions. This complex microdomain has been referred to as the intracellular energetic unit. Here, we review the literature in support of the notion that cardiac homeostasis and disease are emergent properties of the hierarchical organization of these units. Specifically, we will focus on pathological alterations of this microdomain that result in cardiac diseases through energy imbalance and posttranslational modifications of the cytoskeletal proteins involved in mechanosensing and transduction.
Published Version: doi:10.1155/2016/4081638
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5164897/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:30371143
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