Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases

Vascular smooth muscle cells (VSMCs), the major cell type in the arterial vessel wall, have a contractile phenotype that maintains the normal vessel structure and function under physiological conditions. In response to stress or vascular injury, contractile VSMCs can switch to a less differentiated...

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Main Authors: Hao-Yue Tang, Ai-Qun Chen, Huan Zhang, Xiao-Fei Gao, Xiang-Quan Kong, Jun-Jie Zhang
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/24/4060
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author Hao-Yue Tang
Ai-Qun Chen
Huan Zhang
Xiao-Fei Gao
Xiang-Quan Kong
Jun-Jie Zhang
author_facet Hao-Yue Tang
Ai-Qun Chen
Huan Zhang
Xiao-Fei Gao
Xiang-Quan Kong
Jun-Jie Zhang
author_sort Hao-Yue Tang
collection DOAJ
description Vascular smooth muscle cells (VSMCs), the major cell type in the arterial vessel wall, have a contractile phenotype that maintains the normal vessel structure and function under physiological conditions. In response to stress or vascular injury, contractile VSMCs can switch to a less differentiated state (synthetic phenotype) to acquire the proliferative, migratory, and synthetic capabilities for tissue reparation. Imbalances in VSMCs phenotypic switching can result in a variety of cardiovascular diseases, including atherosclerosis, in-stent restenosis, aortic aneurysms, and vascular calcification. It is very important to identify the molecular mechanisms regulating VSMCs phenotypic switching to prevent and treat cardiovascular diseases with high morbidity and mortality. However, the key molecular mechanisms and signaling pathways participating in VSMCs phenotypic switching have still not been fully elucidated despite long-term efforts by cardiovascular researchers. In this review, we provide an updated summary of the recent studies and systematic knowledge of VSMCs phenotypic switching in atherosclerosis, in-stent restenosis, aortic aneurysms, and vascular calcification, which may help guide future research and provide novel insights into the prevention and treatment of related diseases.
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spelling doaj.art-7d9cc0d3a3ad4e928c9d432d5189b1ed2023-11-24T13:55:06ZengMDPI AGCells2073-44092022-12-011124406010.3390/cells11244060Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular DiseasesHao-Yue Tang0Ai-Qun Chen1Huan Zhang2Xiao-Fei Gao3Xiang-Quan Kong4Jun-Jie Zhang5Department of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaDepartment of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaDepartment of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaDepartment of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaDepartment of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaDepartment of Cardiology, Nanjing First Hospital, Nanjing Medical University, No. 68 Changle Road, Nanjing 210006, ChinaVascular smooth muscle cells (VSMCs), the major cell type in the arterial vessel wall, have a contractile phenotype that maintains the normal vessel structure and function under physiological conditions. In response to stress or vascular injury, contractile VSMCs can switch to a less differentiated state (synthetic phenotype) to acquire the proliferative, migratory, and synthetic capabilities for tissue reparation. Imbalances in VSMCs phenotypic switching can result in a variety of cardiovascular diseases, including atherosclerosis, in-stent restenosis, aortic aneurysms, and vascular calcification. It is very important to identify the molecular mechanisms regulating VSMCs phenotypic switching to prevent and treat cardiovascular diseases with high morbidity and mortality. However, the key molecular mechanisms and signaling pathways participating in VSMCs phenotypic switching have still not been fully elucidated despite long-term efforts by cardiovascular researchers. In this review, we provide an updated summary of the recent studies and systematic knowledge of VSMCs phenotypic switching in atherosclerosis, in-stent restenosis, aortic aneurysms, and vascular calcification, which may help guide future research and provide novel insights into the prevention and treatment of related diseases.https://www.mdpi.com/2073-4409/11/24/4060vascular smooth muscle cellatherosclerosisneointimal hyperplasiaaortic aneurysmsvascular calcification
spellingShingle Hao-Yue Tang
Ai-Qun Chen
Huan Zhang
Xiao-Fei Gao
Xiang-Quan Kong
Jun-Jie Zhang
Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
Cells
vascular smooth muscle cell
atherosclerosis
neointimal hyperplasia
aortic aneurysms
vascular calcification
title Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
title_full Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
title_fullStr Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
title_full_unstemmed Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
title_short Vascular Smooth Muscle Cells Phenotypic Switching in Cardiovascular Diseases
title_sort vascular smooth muscle cells phenotypic switching in cardiovascular diseases
topic vascular smooth muscle cell
atherosclerosis
neointimal hyperplasia
aortic aneurysms
vascular calcification
url https://www.mdpi.com/2073-4409/11/24/4060
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AT xiaofeigao vascularsmoothmusclecellsphenotypicswitchingincardiovasculardiseases
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