Cargando…
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia
AIMS: MicroRNAs (miRs) are involved in endogenous neurogenesis, enhancing of which has been regarded as a potential therapeutic strategy for ischemic stroke treatment; however, whether miR‐199a‐5p mediates postischemic neurogenesis remains unclear. This study aims to investigate the proneurogenesis...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651989/ https://www.ncbi.nlm.nih.gov/pubmed/37349971 http://dx.doi.org/10.1111/cns.14323 |
_version_ | 1785136111863988224 |
---|---|
author | Jin, Hua‐Qian Jiang, Wei‐Feng Zheng, Xin‐Tian Li, Lin Fang, Yan Yang, Yan Hu, Xiao‐Wei Chu, Li‐Sheng |
author_facet | Jin, Hua‐Qian Jiang, Wei‐Feng Zheng, Xin‐Tian Li, Lin Fang, Yan Yang, Yan Hu, Xiao‐Wei Chu, Li‐Sheng |
author_sort | Jin, Hua‐Qian |
collection | PubMed |
description | AIMS: MicroRNAs (miRs) are involved in endogenous neurogenesis, enhancing of which has been regarded as a potential therapeutic strategy for ischemic stroke treatment; however, whether miR‐199a‐5p mediates postischemic neurogenesis remains unclear. This study aims to investigate the proneurogenesis effects of miR‐199a‐5p and its possible mechanism after ischemic stroke. METHODS: Neural stem cells (NSCs) were transfected using Lipofectamine 3000 reagent, and the differentiation of NSCs was evaluated by immunofluorescence and Western blotting. Dual‐luciferase reporter assay was performed to verify the target gene of miR‐199a‐5p. MiR‐199a‐5p agomir/antagomir were injected intracerebroventricularly. The sensorimotor functions were evaluated by neurobehavioral tests, infarct volume was measured by toluidine blue staining, neurogenesis was detected by immunofluorescence assay, and the protein levels of neuronal nuclei (NeuN), glial fibrillary acidic protein (GFAP), caveolin‐1 (Cav‐1), vascular endothelial growth factor (VEGF), and brain‐derived neurotrophic factor (BDNF) were measured by Western blotting. RESULTS: MiR‐199a‐5p mimic enhanced neuronal differentiation and inhibited astrocyte differentiation of NSCs, while a miR‐199a‐5p inhibitor induced the opposite effects, which can be reversed by Cav‐1 siRNA. Cav‐1 was through the dual‐luciferase reporter assay confirmed as a target gene of miR‐199a‐5p. miR‐199a‐5p agomir in rat stroke models manifested multiple benefits, such as improving neurological deficits, reducing infarct volume, promoting neurogenesis, inhibiting Cav‐1, and increasing VEGF and BDNF, which was reversed by the miR‐199a‐5p antagomir. CONCLUSION: MiR‐199a‐5p may target and inhibit Cav‐1 to enhance neurogenesis and thus promote functional recovery after cerebral ischemia. These findings indicate that miR‐199a‐5p is a promising target for the treatment of ischemic stroke. |
format | Online Article Text |
id | pubmed-10651989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106519892023-06-22 MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia Jin, Hua‐Qian Jiang, Wei‐Feng Zheng, Xin‐Tian Li, Lin Fang, Yan Yang, Yan Hu, Xiao‐Wei Chu, Li‐Sheng CNS Neurosci Ther Original Articles AIMS: MicroRNAs (miRs) are involved in endogenous neurogenesis, enhancing of which has been regarded as a potential therapeutic strategy for ischemic stroke treatment; however, whether miR‐199a‐5p mediates postischemic neurogenesis remains unclear. This study aims to investigate the proneurogenesis effects of miR‐199a‐5p and its possible mechanism after ischemic stroke. METHODS: Neural stem cells (NSCs) were transfected using Lipofectamine 3000 reagent, and the differentiation of NSCs was evaluated by immunofluorescence and Western blotting. Dual‐luciferase reporter assay was performed to verify the target gene of miR‐199a‐5p. MiR‐199a‐5p agomir/antagomir were injected intracerebroventricularly. The sensorimotor functions were evaluated by neurobehavioral tests, infarct volume was measured by toluidine blue staining, neurogenesis was detected by immunofluorescence assay, and the protein levels of neuronal nuclei (NeuN), glial fibrillary acidic protein (GFAP), caveolin‐1 (Cav‐1), vascular endothelial growth factor (VEGF), and brain‐derived neurotrophic factor (BDNF) were measured by Western blotting. RESULTS: MiR‐199a‐5p mimic enhanced neuronal differentiation and inhibited astrocyte differentiation of NSCs, while a miR‐199a‐5p inhibitor induced the opposite effects, which can be reversed by Cav‐1 siRNA. Cav‐1 was through the dual‐luciferase reporter assay confirmed as a target gene of miR‐199a‐5p. miR‐199a‐5p agomir in rat stroke models manifested multiple benefits, such as improving neurological deficits, reducing infarct volume, promoting neurogenesis, inhibiting Cav‐1, and increasing VEGF and BDNF, which was reversed by the miR‐199a‐5p antagomir. CONCLUSION: MiR‐199a‐5p may target and inhibit Cav‐1 to enhance neurogenesis and thus promote functional recovery after cerebral ischemia. These findings indicate that miR‐199a‐5p is a promising target for the treatment of ischemic stroke. John Wiley and Sons Inc. 2023-06-22 /pmc/articles/PMC10651989/ /pubmed/37349971 http://dx.doi.org/10.1111/cns.14323 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Jin, Hua‐Qian Jiang, Wei‐Feng Zheng, Xin‐Tian Li, Lin Fang, Yan Yang, Yan Hu, Xiao‐Wei Chu, Li‐Sheng MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title |
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title_full |
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title_fullStr |
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title_full_unstemmed |
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title_short |
MiR‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting Cav‐1 after cerebral ischemia |
title_sort | mir‐199a‐5p enhances neuronal differentiation of neural stem cells and promotes neurogenesis by targeting cav‐1 after cerebral ischemia |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651989/ https://www.ncbi.nlm.nih.gov/pubmed/37349971 http://dx.doi.org/10.1111/cns.14323 |
work_keys_str_mv | AT jinhuaqian mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT jiangweifeng mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT zhengxintian mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT lilin mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT fangyan mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT yangyan mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT huxiaowei mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia AT chulisheng mir199a5penhancesneuronaldifferentiationofneuralstemcellsandpromotesneurogenesisbytargetingcav1aftercerebralischemia |