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Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia

The intrinsic ability of neurogenesis after stroke has been proven weak, which results in insufficient repair of injury in the nerve system. Recent studies suggest multiple microRNAs (miRNAs) are involved in the neuroremodeling process. Targeted miRNAs delivery for amplification of neurogenesis is p...

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Detalles Bibliográficos
Autores principales: Yang, Jialei, Zhang, Xiufen, Chen, Xiangjie, Wang, Lei, Yang, Guodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415550/
https://www.ncbi.nlm.nih.gov/pubmed/28624203
http://dx.doi.org/10.1016/j.omtn.2017.04.010
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author Yang, Jialei
Zhang, Xiufen
Chen, Xiangjie
Wang, Lei
Yang, Guodong
author_facet Yang, Jialei
Zhang, Xiufen
Chen, Xiangjie
Wang, Lei
Yang, Guodong
author_sort Yang, Jialei
collection PubMed
description The intrinsic ability of neurogenesis after stroke has been proven weak, which results in insufficient repair of injury in the nerve system. Recent studies suggest multiple microRNAs (miRNAs) are involved in the neuroremodeling process. Targeted miRNAs delivery for amplification of neurogenesis is promising in promoting the prognosis after ischemia. Here, we showed that modified exosomes, with rabies virus glycoprotein (RVG) fused to exosomal protein lysosome-associated membrane glycoprotein 2b (Lamp2b), could efficiently deliver miR-124 to the infarct site. Systemic administration of RVG-exosomes loaded with miR-124 promoted cortical neural progenitors to obtain neuronal identity and protect against ischemic injury by robust cortical neurogenesis. Our study suggests that RVG-exosomes can be utilized therapeutically for the targeted delivery of gene drugs to the brain, thus having great potential for clinical applications.
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spelling pubmed-54155502017-05-05 Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia Yang, Jialei Zhang, Xiufen Chen, Xiangjie Wang, Lei Yang, Guodong Mol Ther Nucleic Acids Original Article The intrinsic ability of neurogenesis after stroke has been proven weak, which results in insufficient repair of injury in the nerve system. Recent studies suggest multiple microRNAs (miRNAs) are involved in the neuroremodeling process. Targeted miRNAs delivery for amplification of neurogenesis is promising in promoting the prognosis after ischemia. Here, we showed that modified exosomes, with rabies virus glycoprotein (RVG) fused to exosomal protein lysosome-associated membrane glycoprotein 2b (Lamp2b), could efficiently deliver miR-124 to the infarct site. Systemic administration of RVG-exosomes loaded with miR-124 promoted cortical neural progenitors to obtain neuronal identity and protect against ischemic injury by robust cortical neurogenesis. Our study suggests that RVG-exosomes can be utilized therapeutically for the targeted delivery of gene drugs to the brain, thus having great potential for clinical applications. American Society of Gene & Cell Therapy 2017-04-13 /pmc/articles/PMC5415550/ /pubmed/28624203 http://dx.doi.org/10.1016/j.omtn.2017.04.010 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Yang, Jialei
Zhang, Xiufen
Chen, Xiangjie
Wang, Lei
Yang, Guodong
Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title_full Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title_fullStr Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title_full_unstemmed Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title_short Exosome Mediated Delivery of miR-124 Promotes Neurogenesis after Ischemia
title_sort exosome mediated delivery of mir-124 promotes neurogenesis after ischemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415550/
https://www.ncbi.nlm.nih.gov/pubmed/28624203
http://dx.doi.org/10.1016/j.omtn.2017.04.010
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