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细胞外囊泡 ncRNA 介导的细胞间通讯在心血管疾病中的研究进展。

Advances in Intercellular Communication Mediated by Exosomal ncRNAs in Cardiovascular Disease.

机构信息

College of Animal Science, Xinjiang Agricultural University, Urumqi 830052, China.

Key Laboratory of Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, Xianyang 712100, China.

出版信息

Int J Mol Sci. 2023 Nov 11;24(22):16197. doi: 10.3390/ijms242216197.


DOI:10.3390/ijms242216197
PMID:38003385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10671547/
Abstract

Cardiovascular diseases are a leading cause of worldwide mortality, and exosomes have recently gained attention as key mediators of intercellular communication in these diseases. Exosomes are double-layered lipid vesicles that can carry biomolecules such as miRNAs, lncRNAs, and circRNAs, and the content of exosomes is dependent on the cell they originated from. They can be involved in the pathophysiological processes of cardiovascular diseases and hold potential as diagnostic and monitoring tools. Exosomes mediate intercellular communication, stimulate or inhibit the activity of target cells, and affect myocardial hypertrophy, injury and infarction, ventricular remodeling, angiogenesis, and atherosclerosis. Exosomes can be released from various types of cells, including endothelial cells, smooth muscle cells, cardiomyocytes, fibroblasts, platelets, adipocytes, immune cells, and stem cells. In this review, we highlight the communication between different cell-derived exosomes and cardiovascular cells, with a focus on the roles of RNAs. This provides new insights for further exploring targeted therapies in the clinical management of cardiovascular diseases.

摘要

心血管疾病是全球死亡率的主要原因,最近,外泌体作为这些疾病中细胞间通讯的关键介质引起了人们的关注。外泌体是双层脂质囊泡,可以携带生物分子,如 miRNA、lncRNA 和 circRNA,并且外泌体的含量取决于它们起源的细胞。它们可以参与心血管疾病的病理生理过程,并具有作为诊断和监测工具的潜力。外泌体介导细胞间通讯,刺激或抑制靶细胞的活性,并影响心肌肥大、损伤和梗死、心室重构、血管生成和动脉粥样硬化。外泌体可以从多种类型的细胞中释放出来,包括内皮细胞、平滑肌细胞、心肌细胞、成纤维细胞、血小板、脂肪细胞、免疫细胞和干细胞。在这篇综述中,我们强调了不同细胞来源的外泌体与心血管细胞之间的通讯,重点介绍了 RNA 的作用。这为进一步探索心血管疾病临床管理中的靶向治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/10671547/74f63a106d35/ijms-24-16197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/10671547/02b459a83e57/ijms-24-16197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/10671547/74f63a106d35/ijms-24-16197-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/10671547/02b459a83e57/ijms-24-16197-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/10671547/74f63a106d35/ijms-24-16197-g002.jpg

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引用本文的文献

[1]
Exosomal non-coding RNAs: key molecules in the diagnosis and treatment of coronary artery disease.

PeerJ. 2025-6-10

[2]
Exosomal non-coding RNAs in the regulation of bone metabolism homeostasis: Molecular mechanism and therapeutic potential.

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[3]
Extracellular vesicular microRNAs and cardiac hypertrophy.

Front Endocrinol (Lausanne). 2025-1-9

[4]
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Biomolecules. 2024-10-24

[5]
Special Issue "The Role of Non-Coding RNAs Involved in Cardiovascular Diseases and Cellular Communication".

Int J Mol Sci. 2024-5-30

[6]
Assessing biomarkers for post-surgical wound healing: A meta-analysis of exosome-based CircRNA in breast cancer recovery.

Int Wound J. 2024-2

本文引用的文献

[1]
Exosomal miR-27b-3p secreted by visceral adipocytes contributes to endothelial inflammation and atherogenesis.

Cell Rep. 2023-1-31

[2]
Atrial myocyte-derived exosomal microRNA contributes to atrial fibrosis in atrial fibrillation.

J Transl Med. 2022-9-5

[3]
Cardiac Fibroblasts Promote Ferroptosis in Atrial Fibrillation by Secreting Exo-miR-23a-3p Targeting SLC7A11.

Oxid Med Cell Longev. 2022

[4]
Epididymal white adipose tissue promotes angiotensin II-induced cardiac fibrosis in an exosome-dependent manner.

Transl Res. 2022-10

[5]
Role of exosomal non-coding RNAs from tumor cells and tumor-associated macrophages in the tumor microenvironment.

Mol Ther. 2022-10-5

[6]
Therapeutic Potential of Exosomes Derived From circRNA_0002113 Lacking Mesenchymal Stem Cells in Myocardial Infarction.

Front Cell Dev Biol. 2022-1-19

[7]
lncRNA Nuclear Factor of Activated T Cells Knockdown Alleviates Hypoxia/Reoxygenation-induced Cardiomyocyte Apoptosis by Upregulating HIF-1α Expression.

J Cardiovasc Pharmacol. 2022-4-1

[8]
Endothelial cell-derived exosomal circHIPK3 promotes the proliferation of vascular smooth muscle cells induced by high glucose via the miR-106a-5p/Foxo1/Vcam1 pathway.

Aging (Albany NY). 2021-12-10

[9]
CircNPHP4 in monocyte-derived small extracellular vesicles controls heterogeneous adhesion in coronary heart atherosclerotic disease.

Cell Death Dis. 2021-10-14

[10]
Percutaneous Coronary Intervention (PCI) Reprograms Circulating Extracellular Vesicles from ACS Patients Impairing Their Cardio-Protective Properties.

Int J Mol Sci. 2021-9-24

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