Abstract |
Transient focal ischemia induces a sustained downregulation of miR-7 leading to derepression of its target α- synuclein (α-Syn), which promotes neuronal death. We previously showed that treatment with miR-7 mimic prevents α-Syn induction and protects brain after stroke in rodents irrespective of age and sex. To further decipher the role of miR-7, we currently studied infarction and motor function in miR-7 double knockout mice (lack both miR-7a and miR-7b) subjected to focal ischemia. Adult miR-7-/- mice showed similar motor and cognitive functions to miR-7+/+ mice. However, when subjected to even a mild focal ischemia, the miR-7-/- mice showed exacerbated brain damage and worsened motor function compared with the miR-7+/+ mice. Replenishing miR-7 in miR-7-/- mice (IV injection of miR-7 mimic) restored miR-7 mediated neuroprotection and motor recovery, potentially by preventing α-Syn protein induction. Thus, we show that miR-7 is an essential miRNA in the brain that prevents α-Syn translation and the ensuing brain damage after stroke.
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Authors | Suresh L Mehta, Anil K Chokkalla, Saivenkateshkomal Bathula, Raghu Vemuganti |
Journal | Translational stroke research
(Transl Stroke Res)
Vol. 14
Issue 1
Pg. 111-115
(02 2023)
ISSN: 1868-601X [Electronic] United States |
PMID | 35088373
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, N.I.H., Extramural)
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Copyright | © 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. |
Chemical References |
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Topics |
- Mice
- Animals
- Stroke
(genetics, metabolism)
- MicroRNAs
(genetics, metabolism)
- Brain Ischemia
(metabolism)
- Brain
(metabolism)
- Mice, Knockout
- Mice, Inbred C57BL
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