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Protein disulfide isomerase in cardiovascular disease

Protein disulfide isomerase (PDI) participates in the pathogenesis of numerous diseases. Increasing evidence indicates that intravascular cell-derived PDI plays an important role in the initiation and progression of cardiovascular diseases, including thrombosis and vascular inflammation. Recent stud...

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Autores principales: Xiong, Bei, Jha, Vishwanath, Min, Jeong-Ki, Cho, Jaehyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156431/
https://www.ncbi.nlm.nih.gov/pubmed/32203104
http://dx.doi.org/10.1038/s12276-020-0401-5
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author Xiong, Bei
Jha, Vishwanath
Min, Jeong-Ki
Cho, Jaehyung
author_facet Xiong, Bei
Jha, Vishwanath
Min, Jeong-Ki
Cho, Jaehyung
author_sort Xiong, Bei
collection PubMed
description Protein disulfide isomerase (PDI) participates in the pathogenesis of numerous diseases. Increasing evidence indicates that intravascular cell-derived PDI plays an important role in the initiation and progression of cardiovascular diseases, including thrombosis and vascular inflammation. Recent studies with PDI conditional knockout mice have advanced our understanding of the function of cell-specific PDI in disease processes. Furthermore, the identification and development of novel small-molecule PDI inhibitors has led into a new era of PDI research that transitioned from the bench to bedside. In this review, we will discuss recent findings on the regulatory role of PDI in cardiovascular disease.
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spelling pubmed-71564312020-04-20 Protein disulfide isomerase in cardiovascular disease Xiong, Bei Jha, Vishwanath Min, Jeong-Ki Cho, Jaehyung Exp Mol Med Review Article Protein disulfide isomerase (PDI) participates in the pathogenesis of numerous diseases. Increasing evidence indicates that intravascular cell-derived PDI plays an important role in the initiation and progression of cardiovascular diseases, including thrombosis and vascular inflammation. Recent studies with PDI conditional knockout mice have advanced our understanding of the function of cell-specific PDI in disease processes. Furthermore, the identification and development of novel small-molecule PDI inhibitors has led into a new era of PDI research that transitioned from the bench to bedside. In this review, we will discuss recent findings on the regulatory role of PDI in cardiovascular disease. Nature Publishing Group UK 2020-03-18 /pmc/articles/PMC7156431/ /pubmed/32203104 http://dx.doi.org/10.1038/s12276-020-0401-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Xiong, Bei
Jha, Vishwanath
Min, Jeong-Ki
Cho, Jaehyung
Protein disulfide isomerase in cardiovascular disease
title Protein disulfide isomerase in cardiovascular disease
title_full Protein disulfide isomerase in cardiovascular disease
title_fullStr Protein disulfide isomerase in cardiovascular disease
title_full_unstemmed Protein disulfide isomerase in cardiovascular disease
title_short Protein disulfide isomerase in cardiovascular disease
title_sort protein disulfide isomerase in cardiovascular disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156431/
https://www.ncbi.nlm.nih.gov/pubmed/32203104
http://dx.doi.org/10.1038/s12276-020-0401-5
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