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基质小泡作为血管钙化的治疗靶点

Matrix Vesicles as a Therapeutic Target for Vascular Calcification.

作者信息

Li Tiantian, Yu Hongchi, Zhang Demao, Feng Tang, Miao Michael, Li Jianwei, Liu Xiaoheng

机构信息

Institute of Biomedical Engineering, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, China.

Division of Oral & Craniofacial Health Sciences, University of North Carolina Adams School of Dentistry, Chapel Hill, NC, United States.

出版信息

Front Cell Dev Biol. 2022 Jan 21;10:825622. doi: 10.3389/fcell.2022.825622. eCollection 2022.

Abstract

Vascular calcification (VC) is linked to an increased risk of heart disease, stroke, and atherosclerotic plaque rupture. It is a cell-active process regulated by vascular cells rather than pure passive calcium (Ca) deposition. In recent years, extracellular vesicles (EVs) have attracted extensive attention because of their essential role in the process of VC. Matrix vesicles (MVs), one type of EVs, are especially critical in extracellular matrix mineralization and the early stages of the development of VC. Vascular smooth muscle cells (VSMCs) have the potential to undergo phenotypic transformation and to serve as a nucleation site for hydroxyapatite crystals upon extracellular stimulation. However, it is not clear what underlying mechanism that MVs drive the VSMCs phenotype switching and to result in calcification. This article aims to review the detailed role of MVs in the progression of VC and compare the difference with other major drivers of calcification, including aging, uremia, mechanical stress, oxidative stress, and inflammation. We will also bring attention to the novel findings in the isolation and characterization of MVs, and the therapeutic application of MVs in VC.

摘要

血管钙化(VC)与心脏病、中风和动脉粥样硬化斑块破裂风险增加有关。它是一个由血管细胞调节的细胞活性过程,而非单纯的被动钙(Ca)沉积。近年来,细胞外囊泡(EVs)因其在VC过程中的重要作用而备受关注。基质囊泡(MVs)作为EVs的一种类型,在细胞外基质矿化和VC发展的早期阶段尤为关键。血管平滑肌细胞(VSMCs)在细胞外刺激下具有发生表型转化并作为羟基磷灰石晶体成核位点的潜力。然而,尚不清楚MVs驱动VSMCs表型转换并导致钙化的潜在机制是什么。本文旨在综述MVs在VC进展中的详细作用,并比较其与钙化的其他主要驱动因素(包括衰老、尿毒症、机械应力、氧化应激和炎症)的差异。我们还将关注MVs分离和表征方面的新发现,以及MVs在VC中的治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/275d/8814528/2ee2853ad2b2/fcell-10-825622-g001.jpg

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