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Heat Shock Protein 60 in Cardiovascular Physiology and Diseases
Heat shock protein 60 (HSP60) is a highly conserved protein abundantly expressed in both prokaryotic and eukaryotic cells. In mammals, HSP60 has been primarily considered to reside in the mitochondria, where HSP60 and HSP10 form a complex and facilitate mitochondrial protein folding. However, HSP60...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203681/ https://www.ncbi.nlm.nih.gov/pubmed/32426370 http://dx.doi.org/10.3389/fmolb.2020.00073 |
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author | Duan, Yaoyun Tang, Huayuan Mitchell-silbaugh, Kali Fang, Xi Han, Zhen Ouyang, Kunfu |
author_facet | Duan, Yaoyun Tang, Huayuan Mitchell-silbaugh, Kali Fang, Xi Han, Zhen Ouyang, Kunfu |
author_sort | Duan, Yaoyun |
collection | PubMed |
description | Heat shock protein 60 (HSP60) is a highly conserved protein abundantly expressed in both prokaryotic and eukaryotic cells. In mammals, HSP60 has been primarily considered to reside in the mitochondria, where HSP60 and HSP10 form a complex and facilitate mitochondrial protein folding. However, HSP60 is also observed in the cytoplasm, the plasma membrane, and the extracellular space. HSP60 regulates a broad spectrum of cellular events including protein trafficking, peptide hormone signaling, cell survival, cell proliferation, inflammation, and immunization. In the cardiovascular system, growing evidence indicates that HSP60 could not only play an important role under physiological conditions, but also regulate the initiation and progression of heart failure and atherosclerosis. In this review, we focus on recent progress in understanding the function of HSP60 in cardiomyocytes, endothelial cells, and vascular smooth muscle cells (VSMCs), respectively, and discuss the related signaling pathways that have been found in these cells, so as to illustrate the role of HSP60 in the development of cardiovascular disease. |
format | Online Article Text |
id | pubmed-7203681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72036812020-05-18 Heat Shock Protein 60 in Cardiovascular Physiology and Diseases Duan, Yaoyun Tang, Huayuan Mitchell-silbaugh, Kali Fang, Xi Han, Zhen Ouyang, Kunfu Front Mol Biosci Molecular Biosciences Heat shock protein 60 (HSP60) is a highly conserved protein abundantly expressed in both prokaryotic and eukaryotic cells. In mammals, HSP60 has been primarily considered to reside in the mitochondria, where HSP60 and HSP10 form a complex and facilitate mitochondrial protein folding. However, HSP60 is also observed in the cytoplasm, the plasma membrane, and the extracellular space. HSP60 regulates a broad spectrum of cellular events including protein trafficking, peptide hormone signaling, cell survival, cell proliferation, inflammation, and immunization. In the cardiovascular system, growing evidence indicates that HSP60 could not only play an important role under physiological conditions, but also regulate the initiation and progression of heart failure and atherosclerosis. In this review, we focus on recent progress in understanding the function of HSP60 in cardiomyocytes, endothelial cells, and vascular smooth muscle cells (VSMCs), respectively, and discuss the related signaling pathways that have been found in these cells, so as to illustrate the role of HSP60 in the development of cardiovascular disease. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7203681/ /pubmed/32426370 http://dx.doi.org/10.3389/fmolb.2020.00073 Text en Copyright © 2020 Duan, Tang, Mitchell-silbaugh, Fang, Han and Ouyang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Duan, Yaoyun Tang, Huayuan Mitchell-silbaugh, Kali Fang, Xi Han, Zhen Ouyang, Kunfu Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title | Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title_full | Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title_fullStr | Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title_full_unstemmed | Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title_short | Heat Shock Protein 60 in Cardiovascular Physiology and Diseases |
title_sort | heat shock protein 60 in cardiovascular physiology and diseases |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203681/ https://www.ncbi.nlm.nih.gov/pubmed/32426370 http://dx.doi.org/10.3389/fmolb.2020.00073 |
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