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心脏细胞来源的外泌体中微小RNA在细胞间通讯中的调控机制

Regulation mechanism of microRNAs in cardiac cells-derived exosomes in cell crosstalk.

作者信息

Lin Shanshan, Yang Yuanjian, Zhou Zhou, Li Wen, Wang Xianliang, Liu Yu, Bi Yingfei, Mao Jingyuan

机构信息

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin, China.

Tianjin University of Traditional Chinese Medicine, Tianjin, China.

出版信息

Front Pharmacol. 2024 Aug 20;15:1399850. doi: 10.3389/fphar.2024.1399850. eCollection 2024.

DOI:10.3389/fphar.2024.1399850
PMID:39228519
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11368792/
Abstract

The heart is a multicellular system, and the intercellular crosstalk mechanism is very important for the growth and development of the heart and even the organs, tissues, and cells at a distance. As a kind of extracellular vesicle, exosomes are released by different types of cells and can carry specific genetic material, endosomal proteins, cytokines, etc., which are the main material basis for mediating cell crosstalk mechanism. Among them, microRNA carried by cardiac cells-derived exosomes have highly conserved sequences and play a key role in regulating the function of organs, tissues, and cells related to cardiovascular diseases and their complications and comorbidities, which have attracted extensive attention in the medical community in recent years. Following up on the latest research progress at home and abroad, this review systematically summarized the regulatory role of microRNA from cardiac cells-derived exosomes in various cell crosstalk, including not only cardiac cells (including cardiomyocytes, fibroblasts, myofibroblast, cardiac progenitor cells, cardiac microvascular endothelial cells, cardiosphere-derived cells, etc.) but also tumor cells, bone marrow progenitor cells, and other tissue cells, in order to provide a reference for the prevention and treatment of cardiovascular diseases and their complications and comorbidities.

摘要

心脏是一个多细胞系统,细胞间的相互作用机制对于心脏乃至远处的器官、组织和细胞的生长发育都非常重要。作为一种细胞外囊泡,外泌体由不同类型的细胞释放,可携带特定的遗传物质、内体蛋白、细胞因子等,是介导细胞间相互作用机制的主要物质基础。其中,心脏细胞来源的外泌体携带的微小RNA具有高度保守的序列,在调节与心血管疾病及其并发症和合并症相关的器官、组织和细胞功能方面发挥着关键作用,近年来在医学界引起了广泛关注。本文追踪国内外最新研究进展,系统总结了心脏细胞来源的外泌体中微小RNA在各种细胞间相互作用中的调节作用,这些细胞不仅包括心脏细胞(包括心肌细胞、成纤维细胞、肌成纤维细胞、心脏祖细胞、心脏微血管内皮细胞、心脏球衍生细胞等),还包括肿瘤细胞、骨髓祖细胞和其他组织细胞,以期为心血管疾病及其并发症和合并症的防治提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e561/11368792/da5facc79c57/fphar-15-1399850-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e561/11368792/da5facc79c57/fphar-15-1399850-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e561/11368792/da5facc79c57/fphar-15-1399850-g001.jpg

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本文引用的文献

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Exosomes secreted from cardiomyocytes suppress the sensitivity of tumor ferroptosis in ischemic heart failure.心肌细胞分泌的外泌体抑制缺血性心力衰竭中肿瘤细胞的铁死亡敏感性。
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Hypoxic cardiomyocyte-derived exosomes regulate cardiac fibroblast activation, apoptosis, migration and ferroptosis through miR-208a/b.低氧心肌细胞来源的外泌体通过 miR-208a/b 调节心肌成纤维细胞的激活、凋亡、迁移和铁死亡。
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Cardiac fibroblasts secrete exosome microRNA to suppress cardiomyocyte pyroptosis in myocardial ischemia/reperfusion injury.
心肌成纤维细胞分泌外泌体 microRNA 抑制心肌缺血/再灌注损伤中的心肌细胞焦亡。
Mol Cell Biochem. 2022 Apr;477(4):1249-1260. doi: 10.1007/s11010-021-04343-7. Epub 2022 Feb 4.
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Myofibroblast-Derived Exosome Induce Cardiac Endothelial Cell Dysfunction.肌成纤维细胞衍生的外泌体诱导心脏内皮细胞功能障碍。
Front Cardiovasc Med. 2021 Apr 23;8:676267. doi: 10.3389/fcvm.2021.676267. eCollection 2021.
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Exosomes Derived From Hypertrophic Cardiomyocytes Induce Inflammation in Macrophages miR-155 Mediated MAPK Pathway.心肌肥厚来源的外泌体通过 miR-155 介导的 MAPK 通路诱导巨噬细胞炎症反应
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Inhibition of Exo-miR-19a-3p derived from cardiomyocytes promotes angiogenesis and improves heart function in mice with myocardial infarction via targeting HIF-1α.心肌细胞来源的外泌体 miR-19a-3p 通过靶向 HIF-1α 抑制促进心肌梗死后小鼠的血管生成和改善心功能。
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