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Role of NFAT in the Progression of Diabetic Atherosclerosis
Nuclear factor of activated T cells (NFAT) is a transcription factor with a multidirectional regulatory function, that is widely expressed in immune cells, including cells in the cardiovascular system, and non-immune cells. A large number of studies have confirmed that calcineurin/NFAT signal transd...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006278/ https://www.ncbi.nlm.nih.gov/pubmed/33791348 http://dx.doi.org/10.3389/fcvm.2021.635172 |
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author | Cai, Yaoyao Yao, Haipeng Sun, Zhen Wang, Ying Zhao, Yunyun Wang, Zhongqun Li, Lihua |
author_facet | Cai, Yaoyao Yao, Haipeng Sun, Zhen Wang, Ying Zhao, Yunyun Wang, Zhongqun Li, Lihua |
author_sort | Cai, Yaoyao |
collection | PubMed |
description | Nuclear factor of activated T cells (NFAT) is a transcription factor with a multidirectional regulatory function, that is widely expressed in immune cells, including cells in the cardiovascular system, and non-immune cells. A large number of studies have confirmed that calcineurin/NFAT signal transduction is very important in the development of vascular system and cardiovascular system during embryonic development, and plays some role in the occurrence of vascular diseases such as atherosclerosis, vascular calcification, and hypertension. Recent in vitro and in vivo studies have shown that NFAT proteins and their activation in the nucleus and binding to DNA-related sites can easily ɨnduce the expression of downstream target genes that participate in the proliferation, migration, angiogenesis, and vascular inflammation of vascular wall related cells in various pathophysiological states. NFAT expression is regulated by various signaling pathways, including CD137-CD137L, and OX40-OX40L pathways. As a functionally diverse transcription factor, NFAT interacts with a large number of signaling molecules to modulate intracellular and extracellular signaling pathways. These NFAT-centered signaling pathways play important regulatory roles in the progression of atherosclerosis, such as in vascular smooth muscle cell phenotypic transition and migration, endothelial cell injury, macrophage-derived foam cell formation, and plaque calcification. NFAT and related signaling pathways provide new therapeutic targets for vascular diseases such as atherosclerosis. Hence, further studies of the mechanism of NFAT in the occurrence and evolution of atherosclerosis remain crucial. |
format | Online Article Text |
id | pubmed-8006278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80062782021-03-30 Role of NFAT in the Progression of Diabetic Atherosclerosis Cai, Yaoyao Yao, Haipeng Sun, Zhen Wang, Ying Zhao, Yunyun Wang, Zhongqun Li, Lihua Front Cardiovasc Med Cardiovascular Medicine Nuclear factor of activated T cells (NFAT) is a transcription factor with a multidirectional regulatory function, that is widely expressed in immune cells, including cells in the cardiovascular system, and non-immune cells. A large number of studies have confirmed that calcineurin/NFAT signal transduction is very important in the development of vascular system and cardiovascular system during embryonic development, and plays some role in the occurrence of vascular diseases such as atherosclerosis, vascular calcification, and hypertension. Recent in vitro and in vivo studies have shown that NFAT proteins and their activation in the nucleus and binding to DNA-related sites can easily ɨnduce the expression of downstream target genes that participate in the proliferation, migration, angiogenesis, and vascular inflammation of vascular wall related cells in various pathophysiological states. NFAT expression is regulated by various signaling pathways, including CD137-CD137L, and OX40-OX40L pathways. As a functionally diverse transcription factor, NFAT interacts with a large number of signaling molecules to modulate intracellular and extracellular signaling pathways. These NFAT-centered signaling pathways play important regulatory roles in the progression of atherosclerosis, such as in vascular smooth muscle cell phenotypic transition and migration, endothelial cell injury, macrophage-derived foam cell formation, and plaque calcification. NFAT and related signaling pathways provide new therapeutic targets for vascular diseases such as atherosclerosis. Hence, further studies of the mechanism of NFAT in the occurrence and evolution of atherosclerosis remain crucial. Frontiers Media S.A. 2021-03-11 /pmc/articles/PMC8006278/ /pubmed/33791348 http://dx.doi.org/10.3389/fcvm.2021.635172 Text en Copyright © 2021 Cai, Yao, Sun, Wang, Zhao, Wang and Li. 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 | Cardiovascular Medicine Cai, Yaoyao Yao, Haipeng Sun, Zhen Wang, Ying Zhao, Yunyun Wang, Zhongqun Li, Lihua Role of NFAT in the Progression of Diabetic Atherosclerosis |
title | Role of NFAT in the Progression of Diabetic Atherosclerosis |
title_full | Role of NFAT in the Progression of Diabetic Atherosclerosis |
title_fullStr | Role of NFAT in the Progression of Diabetic Atherosclerosis |
title_full_unstemmed | Role of NFAT in the Progression of Diabetic Atherosclerosis |
title_short | Role of NFAT in the Progression of Diabetic Atherosclerosis |
title_sort | role of nfat in the progression of diabetic atherosclerosis |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006278/ https://www.ncbi.nlm.nih.gov/pubmed/33791348 http://dx.doi.org/10.3389/fcvm.2021.635172 |
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