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α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies

α-smooth muscle actin, encoded by ACTA2 gene, is an isoform of the vascular smooth muscle actins, typically expressed in the vascular smooth muscle cells contributing to vascular motility and contraction. ACTA2 gene mutations cause a diversity of diffuse vasculopathies such as thoracic aortic aneury...

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Autor principal: Yuan, Shi-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cirurgia Cardiovascular 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762557/
https://www.ncbi.nlm.nih.gov/pubmed/26934405
http://dx.doi.org/10.5935/1678-9741.20150081
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author Yuan, Shi-Min
author_facet Yuan, Shi-Min
author_sort Yuan, Shi-Min
collection PubMed
description α-smooth muscle actin, encoded by ACTA2 gene, is an isoform of the vascular smooth muscle actins, typically expressed in the vascular smooth muscle cells contributing to vascular motility and contraction. ACTA2 gene mutations cause a diversity of diffuse vasculopathies such as thoracic aortic aneurysms and dissections as well as occlusive vascular diseases, including premature coronary artery disease and ischemic stroke. Dynamics of differentiation-specific α-smooth muscle actin in arterial smooth muscle cells and proliferation of the proteins have been well described. Although a variety of research works have been undertaken in terms of modifications of α-smooth muscle actin and mutations of ACTA2 gene and myosin, the underlying mechanisms towards the pathological processes by way of gene mutations are yet to be clarified. The purpose of the present article is to describe the phenotypes of α-smooth muscle actin and implications of ACTA2 mutations in vasculopathies in order to enhance the understanding of potential mechanisms of aortic and coronary disorders.
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spelling pubmed-47625572016-02-24 α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies Yuan, Shi-Min Braz J Cardiovasc Surg Review Article α-smooth muscle actin, encoded by ACTA2 gene, is an isoform of the vascular smooth muscle actins, typically expressed in the vascular smooth muscle cells contributing to vascular motility and contraction. ACTA2 gene mutations cause a diversity of diffuse vasculopathies such as thoracic aortic aneurysms and dissections as well as occlusive vascular diseases, including premature coronary artery disease and ischemic stroke. Dynamics of differentiation-specific α-smooth muscle actin in arterial smooth muscle cells and proliferation of the proteins have been well described. Although a variety of research works have been undertaken in terms of modifications of α-smooth muscle actin and mutations of ACTA2 gene and myosin, the underlying mechanisms towards the pathological processes by way of gene mutations are yet to be clarified. The purpose of the present article is to describe the phenotypes of α-smooth muscle actin and implications of ACTA2 mutations in vasculopathies in order to enhance the understanding of potential mechanisms of aortic and coronary disorders. Sociedade Brasileira de Cirurgia Cardiovascular 2015 /pmc/articles/PMC4762557/ /pubmed/26934405 http://dx.doi.org/10.5935/1678-9741.20150081 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Review Article
Yuan, Shi-Min
α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title_full α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title_fullStr α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title_full_unstemmed α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title_short α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies
title_sort α-smooth muscle actin and acta2 gene expressions in vasculopathies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762557/
https://www.ncbi.nlm.nih.gov/pubmed/26934405
http://dx.doi.org/10.5935/1678-9741.20150081
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