Dynamic release of neuronal extracellular vesicles containing miR-21a-5p is induced by hypoxia
Author
Korvenlaita, N.Gómez-Budia, M.
Scoyni, F.
Pistono, C.
Giudice, L.
Eamen, S.
Loppi, S.
de Sande, A.H.
Huremagic, B.
Bouvy-Liivrand, M.
Heinäniemi, M.
Kaikkonen, M.U.
Cheng, L.
Hill, A.F.
Kanninen, K.M.
Jenster, G.W.
van Royen, M.E.
Ramiro, L.
Montaner, J.
Batkova, T.
Mikulik, R.
Giugno, R.
Jolkkonen, J.
Korhonen, P.
Malm, T.
Affiliation
Department of Immunology, University of ArizonaIssue Date
2023-01-03
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TAYLOR & FRANCISCitation
Korvenlaita, N., Gómez‐Budia, M., Scoyni, F., Pistono, C., Giudice, L., Eamen, S., ... & Malm, T. (2023). Dynamic release of neuronal extracellular vesicles containing miR‐21a‐5p is induced by hypoxia. Journal of Extracellular Vesicles, 12(1), 12297.Rights
© 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Hypoxia induces changes in the secretion of extracellular vesicles (EVs) in several non-neuronal cells and pathological conditions. EVs are packed with biomolecules, such as microRNA(miR)-21-5p, which respond to hypoxia. However, the true EV association of miR-21-5p, and its functional or biomarker relevance, are inadequately characterised. Neurons are extremely sensitive cells, and it is not known whether the secretion of neuronal EVs and miR-21-5p are altered upon hypoxia. Here, we characterised the temporal EV secretion profile and cell viability of neurons under hypoxia. Hypoxia induced a rapid increase of miR-21a-5p secretion in the EVs, which preceded the elevation of hypoxia-induced tissue or cellular miR-21a-5p. Prolonged hypoxia induced cell death and the release of morphologically distinct EVs. The EVs protected miR-21a-5p from enzymatic degradation but a remarkable fraction of miR-21a-5p remained fragile and non-EV associated. The increase in miR-21a-5p secretion may have biomarker potential, as high blood levels of miR-21-5p in stroke patients were associated with significant disability at hospital discharge. Our data provides an understanding of the dynamic regulation of EV secretion from neurons under hypoxia and provides a candidate for the prediction of recovery from ischemic stroke. © 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles.Note
Open access journalISSN
2001-3078PubMed ID
36594832Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1002/jev2.12297
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Except where otherwise noted, this item's license is described as © 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles. This is an open access article under the terms of the Creative Commons Attribution License.
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