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解析外泌体:心脏修复的治疗前沿

Unpacking Exosomes: A Therapeutic Frontier for Cardiac Repair.

作者信息

McMullan Elena, Joladarashi Darukeshwara, Kishore Raj

机构信息

Aging and Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, 19140, USA.

Department of Cardiovascular Sciences, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, 19140, USA.

出版信息

Curr Cardiol Rep. 2025 Mar 20;27(1):73. doi: 10.1007/s11886-025-02225-8.

DOI:10.1007/s11886-025-02225-8
PMID:40111702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11925971/
Abstract

PURPOSE OF REVIEW

The rising global prevalence of cardiovascular disease is driving the need for innovative biotherapeutics. Recently, exosomes-extracellular vesicles involved in paracrine signaling have shown promise in aiding heart repair associated with cardiovascular conditions. Their therapeutic potential encompasses several beneficial mechanisms, including anti-fibrosis, anti-inflammation, pro-angiogenesis, anti-oxidation, and anti-apoptosis, all contributing to improved cardiac function. This review provides a comprehensive overview of exosomes and highlights the latest research on their effectiveness in addressing current challenges in regenerative cardiac medicine.

RECENT FINDINGS

Current approaches revolve around elucidating and enhancing how different cell types, cargo, and delivery methods impact healing in a pathological cardiovascular environment. The emerging field of therapeutic exosome research is promising for cardiac regeneration due to the beneficial effects of exosomal cargo. The expansion of mechanistic knowledge and the optimization of techniques are required before standard clinical application.

摘要

综述目的

心血管疾病在全球的患病率不断上升,这推动了对创新生物疗法的需求。最近,参与旁分泌信号传导的外泌体(细胞外囊泡)在辅助与心血管疾病相关的心脏修复方面显示出前景。它们的治疗潜力包括多种有益机制,如抗纤维化、抗炎、促血管生成、抗氧化和抗凋亡,所有这些都有助于改善心脏功能。本综述全面概述了外泌体,并重点介绍了其在应对再生心脏医学当前挑战方面有效性的最新研究。

最新发现

当前的方法围绕阐明和增强不同细胞类型、货物和递送方式如何在病理性心血管环境中影响愈合展开。由于外泌体货物的有益作用,治疗性外泌体研究这一新兴领域对心脏再生很有前景。在标准临床应用之前,需要扩展机制知识并优化技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb0/11925971/98f7c1199490/11886_2025_2225_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb0/11925971/98f7c1199490/11886_2025_2225_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb0/11925971/98f7c1199490/11886_2025_2225_Fig1_HTML.jpg

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本文引用的文献

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2025 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association.《2025年心脏病和中风统计数据:美国心脏协会关于美国和全球数据的报告》
Circulation. 2025 Feb 25;151(8):e41-e660. doi: 10.1161/CIR.0000000000001303. Epub 2025 Jan 27.
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Small Extracellular Vesicles from Young Healthy Human Plasma Inhibit Cardiac Fibrosis After Myocardial Infarction via miR-664a-3p Targeting SMAD4.来自年轻健康人血浆的小细胞外囊泡通过miR-664a-3p靶向SMAD4抑制心肌梗死后的心脏纤维化。
Int J Nanomedicine. 2025 Jan 13;20:557-579. doi: 10.2147/IJN.S488368. eCollection 2025.
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Activation of Imprinted Gene Promotes Cardiac Fibrosis After Ischemic Injury.
印记基因的激活促进缺血性损伤后的心脏纤维化。
Circulation. 2025 Mar 4;151(9):623-639. doi: 10.1161/CIRCULATIONAHA.124.070738. Epub 2024 Dec 20.
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Exosomal miRNA-let-7i-5p from bone marrow mesenchymal stem cells protects against myocardial infarction by inhibiting myocardial apoptosis.骨髓间充质干细胞来源的外泌体miRNA-let-7i-5p通过抑制心肌细胞凋亡来预防心肌梗死。
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Transcription Factor 21 Regulates Cardiac Myofibroblast Formation and Fibrosis.转录因子21调控心肌成纤维细胞的形成与纤维化。
Circ Res. 2025 Jan 3;136(1):44-58. doi: 10.1161/CIRCRESAHA.124.325527. Epub 2024 Dec 4.
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Vericiguat enhances the therapeutic efficacy of mesenchymal stem cells-derived exosomes in acute myocardial infarction through microRNA-1180-3p/ETS1 pathway.维立西呱通过微小RNA-1180-3p/ETS1途径增强间充质干细胞衍生外泌体在急性心肌梗死中的治疗效果。
Cell Signal. 2025 Jan;125:111512. doi: 10.1016/j.cellsig.2024.111512. Epub 2024 Nov 16.
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iScience. 2024 Sep 24;27(10):111021. doi: 10.1016/j.isci.2024.111021. eCollection 2024 Oct 18.
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