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血管壁微环境中的细胞间通讯:外泌体在血管钙化中的作用

Cellular Crosstalk in the Vascular Wall Microenvironment: The Role of Exosomes in Vascular Calcification.

作者信息

Wu Yun-Yun, Shan Su-Kang, Lin Xiao, Xu Feng, Zhong Jia-Yu, Wu Feng, Duan Jia-Yue, Guo Bei, Li Fu-Xing-Zi, Wang Yi, Zheng Ming-Hui, Xu Qiu-Shuang, Lei Li-Min, Ou-Yang Wen-Lu, Tang Ke-Xin, Li Chang-Chun, Ullah Muhammad Hasnain Ehsan, Yuan Ling-Qing

机构信息

Department of Metabolism and Endocrinology, National Clinical Research Center for Metabolic Diseases, The Second Xiangya Hospital, Central South University, Changsha, China.

Department of Radiology, The Second Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Cardiovasc Med. 2022 May 23;9:912358. doi: 10.3389/fcvm.2022.912358. eCollection 2022.


DOI:10.3389/fcvm.2022.912358
PMID:35677687
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9168031/
Abstract

Vascular calcification is prevalent in aging, diabetes, chronic kidney disease, cardiovascular disease, and certain genetic disorders. However, the pathogenesis of vascular calcification is not well-understood. It has been progressively recognized that vascular calcification depends on the bidirectional interactions between vascular cells and their microenvironment. Exosomes are an essential bridge to mediate crosstalk between cells and organisms, and thus they have attracted increased research attention in recent years. Accumulating evidence has indicated that exosomes play an important role in cardiovascular disease, especially in vascular calcification. In this review, we introduce vascular biology and focus on the crosstalk between the different vessel layers and how their interplay controls the process of vascular calcification.

摘要

血管钙化在衰老、糖尿病、慢性肾脏病、心血管疾病及某些遗传疾病中普遍存在。然而,血管钙化的发病机制尚未完全明确。人们逐渐认识到,血管钙化取决于血管细胞与其微环境之间的双向相互作用。外泌体是介导细胞与生物体之间相互作用的重要桥梁,因此近年来受到了越来越多的研究关注。越来越多的证据表明,外泌体在心血管疾病中发挥着重要作用,尤其是在血管钙化方面。在本综述中,我们介绍血管生物学,并重点关注不同血管层之间的相互作用以及它们如何相互影响来控制血管钙化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e69/9168031/f0ecaf08fc0e/fcvm-09-912358-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e69/9168031/eda6ec51b9c9/fcvm-09-912358-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e69/9168031/f0ecaf08fc0e/fcvm-09-912358-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e69/9168031/eda6ec51b9c9/fcvm-09-912358-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e69/9168031/f0ecaf08fc0e/fcvm-09-912358-g0002.jpg

相似文献

[1]
Cellular Crosstalk in the Vascular Wall Microenvironment: The Role of Exosomes in Vascular Calcification.

Front Cardiovasc Med. 2022-5-23

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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Endocrinol Metab (Seoul). 2016-3

[9]
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Funct Integr Genomics. 2019-3-8

[10]
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Trends Cardiovasc Med. 2015-5

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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J Nanobiotechnology. 2023-7-17

[9]
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[10]
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本文引用的文献

[1]
Extracellular Vesicles From LPS-Treated Macrophages Aggravate Smooth Muscle Cell Calcification by Propagating Inflammation and Oxidative Stress.

Front Cell Dev Biol. 2022-3-9

[2]
The Multi-Therapeutic Role of MSCs in Diabetic Nephropathy.

Front Endocrinol (Lausanne). 2021

[3]
A narrative review of exosomes in vascular calcification.

Ann Transl Med. 2021-4

[4]
Exosomes and Obesity-Related Insulin Resistance.

Front Cell Dev Biol. 2021-3-18

[5]
Factors Affecting Extracellular Vesicles Based Drug Delivery Systems.

Molecules. 2021-3-11

[6]
A Novel Peptide-Equipped Exosomes Platform for Delivery of Antisense Oligonucleotides.

ACS Appl Mater Interfaces. 2021-3-10

[7]
Plasma Exosomes Derived From Patients With End-Stage Renal Disease and Renal Transplant Recipients Have Different Effects on Vascular Calcification.

Front Cell Dev Biol. 2021-1-28

[8]
GFOGER Peptide Modifies the Protein Content of Extracellular Vesicles and Inhibits Vascular Calcification.

Front Cell Dev Biol. 2020-11-30

[9]
Reactive Oxygen-Forming Nox5 Links Vascular Smooth Muscle Cell Phenotypic Switching and Extracellular Vesicle-Mediated Vascular Calcification.

Circ Res. 2020-9-11

[10]
S100A9-RAGE Axis Accelerates Formation of Macrophage-Mediated Extracellular Vesicle Microcalcification in Diabetes Mellitus.

Arterioscler Thromb Vasc Biol. 2020-5-28

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