Smooth Muscle Cells in Vascular Remodeling.

Ning Shi, Xiaohan Mei, Shi-You Chen
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引用次数: 44

Abstract

As the primary causes of myocardial infarction, stroke, atherosclerosis, in-stent restenosis, and aneurysm, aortic diseases pose a serious threat to human health. Arterial remodeling is considered to be an important mechanism underlying the development of arterial diseases. Arterial remodeling refers to structural and functional alterations in arterial wall in response to vascular injury or aging. Vascular smooth muscle cells (SMCs), a major component of the arterial wall, exhibit remarkable phenotypic plasticity and can dedifferentiate from a contractile state to a synthetic state, along with increased proliferation and migration abilities.1 Phenotypically modified SMCs play a major role in arterial remodeling.1 Recent publications in ATVB have delineated new pathways or factors that are involved in SMC phenotypic modulation and arterial remodeling. These studies have provided valuable insights for better understanding of regulatory mechanisms responsible for vascular remodeling. This article highlights studies on this topic that have published in ATVB recently.
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血管重构中的平滑肌细胞。
主动脉疾病是导致心肌梗死、脑卒中、动脉粥样硬化、支架内再狭窄、动脉瘤的主要原因,严重威胁着人类的健康。动脉重塑被认为是动脉疾病发生的重要机制。动脉重构是指血管损伤或老化导致的动脉壁结构和功能改变。血管平滑肌细胞(SMCs)是动脉壁的主要组成部分,表现出显著的表型可塑性,可以从收缩状态向合成状态去分化,同时增殖和迁移能力增强表型修饰的SMCs在动脉重塑中起主要作用最近发表在ATVB上的文章描述了参与SMC表型调节和动脉重塑的新途径或因素。这些研究为更好地理解血管重构的调控机制提供了有价值的见解。本文重点介绍了最近在ATVB上发表的关于这一主题的研究。
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Editors and Editorial Board. Correction to: Role of LpL (Lipoprotein Lipase) in Macrophage Polarization In Vitro and In Vivo. Tribute to Paul M. Vanhoutte, MD, PhD (1940-2019). Correction to: 18F-Sodium Fluoride Imaging of Coronary Atherosclerosis in Ambulatory Patients With Diabetes Mellitus. Extracellular MicroRNA-92a Mediates Endothelial Cell-Macrophage Communication.
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