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miRNA in blood-brain barrier repair: role of extracellular vesicles in stroke recovery.

作者信息

Sprincl Vojtech, Romanyuk Nataliya

机构信息

Department of Neuroregeneration, Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czechia.

Department of Neuroscience, 2nd Medical Faculty, Charles University, Prague, Czechia.

出版信息

Front Cell Neurosci. 2025 Feb 7;19:1503193. doi: 10.3389/fncel.2025.1503193. eCollection 2025.


DOI:10.3389/fncel.2025.1503193
PMID:39990970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11842324/
Abstract

Ischemic stroke is a leading cause of mortality and long-term disability globally. One of its aspects is the breakdown of the blood-brain barrier (BBB). The disruption of BBB's integrity during stroke exacerbates neurological damage and hampers therapeutic intervention. Recent advances in regenerative medicine suggest that mesenchymal stem cells (MSCs) derived extracellular vesicles (EVs) show promise for restoring BBB integrity. This review explores the potential of MSC-derived EVs in mediating neuroprotective and reparative effects on the BBB after ischemic stroke. We highlight the molecular cargo of MSC-derived EVs, including miRNAs, and their role in enhancing angiogenesis, promoting the BBB and neural repair, and mitigating apoptosis. Furthermore, we discuss the challenges associated with the clinical translation of MSC-derived EV therapies and the possibilities of further enhancing EVs' innate protective qualities. Our findings underscore the need for further research to optimize the therapeutic potential of EVs and establish their efficacy and safety in clinical settings.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6999/11842324/48bb822f1090/fncel-19-1503193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6999/11842324/63e8601ed006/fncel-19-1503193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6999/11842324/48bb822f1090/fncel-19-1503193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6999/11842324/63e8601ed006/fncel-19-1503193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6999/11842324/48bb822f1090/fncel-19-1503193-g002.jpg

相似文献

[1]
miRNA in blood-brain barrier repair: role of extracellular vesicles in stroke recovery.

Front Cell Neurosci. 2025-2-7

[2]
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Acta Biomater. 2022-12

[3]
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J Nanobiotechnology. 2023-2-28

[4]
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Stem Cells Transl Med. 2015-10

[5]
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[6]
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[7]
Extracellular Vesicles Maintain Blood-Brain Barrier Integrity by the Suppression of Caveolin-1/CD147/VEGFR2/MMP Pathway After Ischemic Stroke.

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[8]
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Front Neurol. 2019-3-12

[9]
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[10]
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引用本文的文献

[1]
The role of stem cell-derived exosomes in regulating pyroptosis for disease therapy.

Stem Cell Res Ther. 2025-7-18

本文引用的文献

[1]
The Impact of the Blood-Brain Barrier and Its Dysfunction in Parkinson's Disease: Contributions to Pathogenesis and Progression.

ACS Omega. 2024-11-5

[2]
2024 Nobel Prize awarded for work on microRNAs.

Lancet. 2024-10-19

[3]
Exosomal miR-486 derived from bone marrow mesenchymal stem cells promotes angiogenesis following cerebral ischemic injury by regulating the PTEN/Akt pathway.

Sci Rep. 2024-8-5

[4]
Extracellular Vesicles Generated by Mesenchymal Stem Cells in Stirred Suspension Bioreactors Promote Angiogenesis in Human-Brain-Derived Endothelial Cells.

Int J Mol Sci. 2024-5-10

[5]
Exploring the intricacies of calcium dysregulation in ischemic stroke: Insights into neuronal cell death and therapeutic strategies.

Life Sci. 2024-6-15

[6]
Mesenchymal stem cell therapy in ischemic stroke trials. A systematic review.

Regen Ther. 2024-4-13

[7]
Cepharanthine maintains integrity of the blood-brain barrier (BBB) in stroke via the VEGF/VEGFR2/ZO-1 signaling pathway.

Aging (Albany NY). 2024-3-21

[8]
Extracellular Vesicles Maintain Blood-Brain Barrier Integrity by the Suppression of Caveolin-1/CD147/VEGFR2/MMP Pathway After Ischemic Stroke.

Int J Nanomedicine. 2024

[9]
Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches.

J Extracell Vesicles. 2024-2

[10]
Recent advances in tissue repair of the blood-brain barrier after stroke.

J Tissue Eng. 2024-1-31

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