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外泌体在缺血性心脏病中的应用的益处与挑战

Beneficial and challenges of exosome application in ischemic heart disease.

作者信息

Mardi Narges, Khanicheragh Parisa, Abbasi-Malati Zahra, Saghebasl Solmaz, Khosrowshahi Nafiseh Didar, Chegeni Sara Aghakhani, Javid Farzin, Azari Mahdiyeh, Salimi Leila, Rezabakhsh Aysa, Milani Soheil Zamen, Rahbarghazi Reza

机构信息

Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Stem Cell Res Ther. 2025 May 19;16(1):247. doi: 10.1186/s13287-025-04363-w.

DOI:10.1186/s13287-025-04363-w
PMID:40390086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12090443/
Abstract

Cardiovascular diseases are the main cause of death and disability in the clinical setting. Among several pathological conditions, myocardial infarction (MI) is a common clinical finding and happens due to the reduction or complete interruption of blood support. Stem cells and progenitors are valid cell sources with significant potential to alleviate several tissue injuries. Differentiation to mature and functional cells and the release of various growth factors, and cytokines are the main reparative mechanisms by which stem cells mediate their reparative tasks. Exosomes (Exos), a subset of extracellular vesicles (EVs), exhibit great theranostic potential in biomedicine. Along with whole-cell-based therapies, the pre-clinical and clinical application of Exos has been extended in animals and humans with ischemic heart diseases (IHD). Here, in this review article, we aimed to highlight the importance of Exos in IHD and address the mechanism of action by focusing on their regenerative potential.

摘要

心血管疾病是临床环境中导致死亡和残疾的主要原因。在几种病理状况中,心肌梗死(MI)是一种常见的临床病症,它是由于血液供应减少或完全中断而发生的。干细胞和祖细胞是有效的细胞来源,具有显著减轻多种组织损伤的潜力。分化为成熟且有功能的细胞以及释放各种生长因子和细胞因子是干细胞介导其修复任务的主要修复机制。外泌体(Exos)是细胞外囊泡(EVs)的一个亚群,在生物医学中展现出巨大的诊疗潜力。随着基于全细胞的疗法,外泌体的临床前和临床应用已在患有缺血性心脏病(IHD)的动物和人类中得到扩展。在此,在这篇综述文章中,我们旨在强调外泌体在缺血性心脏病中的重要性,并通过关注其再生潜力来阐述其作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/41fe05652b01/13287_2025_4363_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/6b333718dc26/13287_2025_4363_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/023a8ef643cb/13287_2025_4363_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/41fe05652b01/13287_2025_4363_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/6b333718dc26/13287_2025_4363_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/5dba91736abe/13287_2025_4363_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/2bf38e5dfd19/13287_2025_4363_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/86d557968d96/13287_2025_4363_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/1ff2647115fa/13287_2025_4363_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/023a8ef643cb/13287_2025_4363_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1c/12090443/41fe05652b01/13287_2025_4363_Fig7_HTML.jpg

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Fundam Res. 2024 Apr 12;5(2):851-867. doi: 10.1016/j.fmre.2024.03.025. eCollection 2025 Mar.
2
Current challenges surrounding exosome treatments.外泌体治疗目前面临的挑战。
Extracell Vesicle. 2023 Dec;2:100023. doi: 10.1016/j.vesic.2023.100023. Epub 2023 Apr 29.
3
The Potential of Mesenchymal Stem Cell-Derived Exosomes in Cardiac Repair.间充质干细胞衍生外泌体在心脏修复中的潜力
Int J Mol Sci. 2024 Dec 17;25(24):13494. doi: 10.3390/ijms252413494.
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Exosome-mediated delivery of CRISPR-Cas9: A revolutionary approach to cancer gene editing.外泌体介导的CRISPR-Cas9递送:癌症基因编辑的革命性方法。
Pathol Res Pract. 2025 Feb;266:155785. doi: 10.1016/j.prp.2024.155785. Epub 2024 Dec 19.
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Exosomes and breast cancer angiogenesis; Highlights in intercellular communication.外泌体与乳腺癌血管生成;细胞间通讯要点
Cancer Cell Int. 2024 Dec 18;24(1):402. doi: 10.1186/s12935-024-03606-9.
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Different storage and freezing protocols for extracellular vesicles: a systematic review.不同的细胞外囊泡储存和冷冻方案:系统综述。
Stem Cell Res Ther. 2024 Nov 26;15(1):453. doi: 10.1186/s13287-024-04005-7.
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Inhibition of miR-194-5p avoids DUSP9 downregulation thus limiting sepsis-induced cardiomyopathy.抑制 miR-194-5p 避免了 DUSP9 的下调,从而限制了脓毒症诱导的心肌病。
Sci Rep. 2024 Sep 2;14(1):20313. doi: 10.1038/s41598-024-71166-z.
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