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Role of Exosomes as a Treatment and Potential Biomarker for Stroke
Abstract
Approximately, 16 million strokes occur worldwide each year, causing 6 million deaths and considerable disability, implying an enormous social, individual health, and economic burden. Due to this high incidence, strategies to promote stroke recovery are urgently needed. Research into new therapeutic approaches for stroke has determined that intravenous administration of mesenchymal stem cells (MSCs) is a good strategy to improve recovery by amplifying mechanisms implicated in brain plasticity. Recent studies have demonstrated the efficacy of MSCs in stroke, with no need for them to reach the area of brain injury. Although the mechanisms by which they mediate restorative effects are still unknown, the evidence suggests that MSCs might use specialised communication by sending and receiving biological information included in elements called exosomes. Exosomes are nanosized extracellular vesicles released into physical environments, and they have recently been suggested to mediate restorative stem cell effects. Moreover, after stroke, exosomes can also be synthesised and released from brain cells, passing through the blood-brain barrier (BBB), and can be detected in peripheral blood or in cerebrospinal fluid. Thus, exosomes could possibly be biomarkers that reflect pathological progress and promote stroke recovery. This review discusses the translational aspects of MSC-derived exosomes and their various roles in brain repair and as circulating biomarkers in stroke.
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“Exosomes are microvesicles with a diameter of 30–150 nm that originate from multivesicular bodies and can participate in intercellular communication by transmitting intracellular proteins, messenger RNAs, miRNAs, and long non-coding RNAs [18–20].”
From CX3CL1/CX3CR1 axis attenuates early brain injury via promoting the delivery of exosomal microRNA-124 from neuron to microglia after subarachnoid hemorrhage (2020) · cites this paper as [20]
Citations
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Increased Circulating Exosomal miRNA-223 Is Associated with Acute Ischemic Stroke
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Cited by
Sorted by citations
Chen, X., Jiang, M., Li, H., Wang, Y., Shen, H., Li, X., Zhang, Y., Wu, J., Yu, Z., & Chen, G. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01882-6 · Cited by 85
miR-124: A Promising Therapeutic Target for Central Nervous System Injuries and Diseases
Xu, J., Zheng, Y., Wang, L., Liu, Y., Wang, X., Li, Y., & Chi, G. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01091-6 · Cited by 55
Metadata
- Authors
- Otero-Ortega, L., Laso-García, F., Gómez-de Frutos, M., Fuentes, B., Diekhorst, L., Díez-Tejedor, E., & Gutiérrez-Fernández, M.
- Venue
- Translational Stroke Research
- Published
- 2018-08-13
- Volume
- 10
- Issue
- 3
- Pages
- 241-249
- ISSN
- 1868-4483
- 1868-601X
- Cited by
- 105
- References
- 6
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
- Funders
- European Commission, H2020 program (RESSTORE project, grant number 681044)
- European Regional Development Fund (FEDER Funding), Research Institute Carlos III, Ministry of Science and Innovation of Spain (CP15/00069, CD12/00706, FI17/00188, PI15/01318, INVICTUS PLUS network (RD16/0019/0005))
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