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间充质干细胞来源的细胞外囊泡和外泌体在治疗氧化应激相关疾病中的研究进展。

Research progress of extracellular vesicles and exosomes derived from mesenchymal stem cells in the treatment of oxidative stress-related diseases.

机构信息

The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan, Guangdong, China.

Department of Pathophysiology, Guangdong Medical University, Dongguan, Guangdong, China.

出版信息

Front Immunol. 2023 Aug 14;14:1238789. doi: 10.3389/fimmu.2023.1238789. eCollection 2023.


DOI:10.3389/fimmu.2023.1238789
PMID:37646039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10461809/
Abstract

There is growing evidence that mesenchymal stem cell-derived extracellular vesicles and exosomes can significantly improve the curative effect of oxidative stress-related diseases. Mesenchymal stem cell extracellular vesicles and exosomes (MSC-EVs and MSC-Exos) are rich in bioactive molecules and have many biological regulatory functions. In this review, we describe how MSC-EVs and MSC-Exos reduce the related markers of oxidative stress and inflammation in various systemic diseases, and the molecular mechanism of MSC-EVs and MSC-Exos in treating apoptosis and vascular injury induced by oxidative stress. The results of a large number of experimental studies have shown that both local and systemic administration can effectively inhibit the oxidative stress response in diseases and promote the survival and regeneration of damaged parenchymal cells. The mRNA and miRNAs in MSC-EVs and MSC-Exos are the most important bioactive molecules in disease treatment, which can inhibit the apoptosis, necrosis and oxidative stress of lung, heart, kidney, liver, bone, skin and other cells, and promote their survive and regenerate.

摘要

越来越多的证据表明,间充质干细胞衍生的细胞外囊泡和外泌体可以显著改善与氧化应激相关的疾病的治疗效果。间充质干细胞细胞外囊泡和外泌体(MSC-EVs 和 MSC-Exos)富含生物活性分子,具有多种生物学调节功能。在这篇综述中,我们描述了 MSC-EVs 和 MSC-Exos 如何降低各种系统性疾病中与氧化应激和炎症相关的标志物,以及 MSC-EVs 和 MSC-Exos 治疗氧化应激诱导的细胞凋亡和血管损伤的分子机制。大量实验研究的结果表明,局部和全身给药均可有效抑制疾病中的氧化应激反应,并促进受损实质细胞的存活和再生。MSC-EVs 和 MSC-Exos 中的 mRNA 和 miRNA 是疾病治疗中最重要的生物活性分子,可抑制肺、心、肾、肝、骨、皮肤等细胞的凋亡、坏死和氧化应激,促进其存活和再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5862/10461809/0b91a7abda03/fimmu-14-1238789-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5862/10461809/455401b29f28/fimmu-14-1238789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5862/10461809/0b91a7abda03/fimmu-14-1238789-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5862/10461809/455401b29f28/fimmu-14-1238789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5862/10461809/0b91a7abda03/fimmu-14-1238789-g002.jpg

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本文引用的文献

[1]
Development of an In Vitro Model of SARS-CoV-Induced Acute Lung Injury for Studying New Therapeutic Approaches.

Antioxidants (Basel). 2022-9-27

[2]
Exosomes Derived from Baicalin-Pretreated Mesenchymal Stem Cells Alleviate Hepatocyte Ferroptosis after Acute Liver Injury via the Keap1-NRF2 Pathway.

Oxid Med Cell Longev. 2022-7-21

[3]
Mesenchymal stem cells-derived small extracellular vesicles alleviate diabetic retinopathy by delivering NEDD4.

Stem Cell Res Ther. 2022-7-15

[4]
Comprehensive proteomic analysis of exosome mimetic vesicles and exosomes derived from human umbilical cord mesenchymal stem cells.

Stem Cell Res Ther. 2022-7-15

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Mesenchymal Stem Cell-Derived Exosome-Loaded microRNA-129-5p Inhibits TRAF3 Expression to Alleviate Apoptosis and Oxidative Stress in Heart Failure.

Cardiovasc Toxicol. 2022-7

[6]
Mesenchymal Stem Cell-Originated Exosomal Lnc A2M-AS1 Alleviates Hypoxia/Reperfusion-Induced Apoptosis and Oxidative Stress in Cardiomyocytes.

Cardiovasc Drugs Ther. 2023-10

[7]
Hypoxic mesenchymal stem cell-derived extracellular vesicles ameliorate renal fibrosis after ischemia-reperfusion injure by restoring CPT1A mediated fatty acid oxidation.

Stem Cell Res Ther. 2022-5-7

[8]
Mesenchymal stem cell-derived exosomal microRNA-182-5p alleviates myocardial ischemia/reperfusion injury by targeting GSDMD in mice.

Cell Death Discov. 2022-4-14

[9]
Extracellular vesicles from hair follicle-derived mesenchymal stromal cells: isolation, characterization and therapeutic potential for chronic wound healing.

Stem Cell Res Ther. 2022-4-8

[10]
HucMSC-derived exosomes delivered BECN1 induces ferroptosis of hepatic stellate cells via regulating the xCT/GPX4 axis.

Cell Death Dis. 2022-4-8

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