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The Application Potential and Advance of Mesenchymal Stem Cell-Derived Exosomes in Myocardial Infarction.

作者信息

Wang Xianyun, Tang Yida, Liu Zhao, Yin Yajuan, Li Quanhai, Liu Gang, Yan Baoyong

机构信息

Cell Therapy Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang, China.

Department of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, China.

出版信息

Stem Cells Int. 2021 Jun 1;2021:5579904. doi: 10.1155/2021/5579904. eCollection 2021.


DOI:10.1155/2021/5579904
PMID:34122557
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8189813/
Abstract

Myocardial infarction (MI) is a devastating disease with high morbidity and mortality caused by the irreversible loss of functional cardiomyocytes and heart failure (HF) due to the restricted blood supply. Mesenchymal stem cells (MSCs) have been emerging as lead candidates to treat MI and subsequent HF mainly through secreting multitudinous factors of which exosomes act as the most effective constituent to boost the repair of heart function through carrying noncoding RNAs and proteins. Given the advantages of higher stability in the circulation, lower toxicity, and controllable transplantation dosage, exosomes have been described as a wonderful and promising cell-free treatment method in cardiovascular disease. Nowadays, MSC-derived exosomes have been proposed as a promising therapeutic approach to improve cardiac function and reverse heart remodeling. However, exosomes' lack of modification cannot result in desired therapeutic effect. Hence, optimized exosomes can be developed via various engineering methods such as pharmacological compound preconditioned MSCs, genetically modified MSCs, or miRNA-loaded exosomes and peptide tagged exosomes to improve the targeting and therapeutic effects of exosomes. The biological characteristics, therapeutic potential, and optimizing strategy of exosomes will be described in our review.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ae6/8189813/c52ed1e85e93/SCI2021-5579904.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ae6/8189813/c52ed1e85e93/SCI2021-5579904.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ae6/8189813/c52ed1e85e93/SCI2021-5579904.001.jpg

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[5]
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本文引用的文献

[1]
Macrophage migration inhibitory factor facilitates the therapeutic efficacy of mesenchymal stem cells derived exosomes in acute myocardial infarction through upregulating miR-133a-3p.

J Nanobiotechnology. 2021-2-27

[2]
Conditioned medium from adipose-derived stem cells attenuates ischemia/reperfusion-induced cardiac injury through the microRNA-221/222/PUMA/ETS-1 pathway.

Theranostics. 2021

[3]
Sources, isolation strategies and therapeutic outcome of exosomes at a glance.

Regen Med. 2020-12

[4]
MicroRNA-221/222 Mediates ADSC-Exosome-Induced Cardioprotection Against Ischemia/Reperfusion by Targeting PUMA and ETS-1.

Front Cell Dev Biol. 2020-12-3

[5]
Exosome and Melatonin Additively Attenuates Inflammation by Transferring miR-34a, miR-124, and miR-135b.

Biomed Res Int. 2020

[6]
Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine.

J Transl Med. 2020-11-27

[7]
MicroRNA-338 in MSCs-derived exosomes inhibits cardiomyocyte apoptosis in myocardial infarction.

Eur Rev Med Pharmacol Sci. 2020-10

[8]
Circular RNA 0001273 in exosomes derived from human umbilical cord mesenchymal stem cells (UMSCs) in myocardial infarction.

Eur Rev Med Pharmacol Sci. 2020-10

[9]
Exosome: A Review of Its Classification, Isolation Techniques, Storage, Diagnostic and Targeted Therapy Applications.

Int J Nanomedicine. 2020-9-22

[10]
Adipose derived mesenchymal stem cell exosomes loaded with miR-10a promote the differentiation of Th17 and Treg from naive CD4 T cell.

Life Sci. 2020-8-9

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