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Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS
Astroglia play active and diverse roles in modulating neuronal/synaptic functions in the CNS. How these astroglial functions are regulated, especially by neuronal signals, remains largely unknown. Exosomes, a major type of extracellular vesicles (EVs) that originate from endosomal intraluminal vesic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742670/ https://www.ncbi.nlm.nih.gov/pubmed/31515491 http://dx.doi.org/10.1038/s41467-019-11534-w |
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author | Men, Yuqin Yelick, Julia Jin, Shijie Tian, Yang Chiang, Ming Sum R. Higashimori, Haruki Brown, Eoin Jarvis, Rachel Yang, Yongjie |
author_facet | Men, Yuqin Yelick, Julia Jin, Shijie Tian, Yang Chiang, Ming Sum R. Higashimori, Haruki Brown, Eoin Jarvis, Rachel Yang, Yongjie |
author_sort | Men, Yuqin |
collection | PubMed |
description | Astroglia play active and diverse roles in modulating neuronal/synaptic functions in the CNS. How these astroglial functions are regulated, especially by neuronal signals, remains largely unknown. Exosomes, a major type of extracellular vesicles (EVs) that originate from endosomal intraluminal vesicles (ILVs), have emerged as a new intercellular communication process. By generating cell-type-specific ILVs/exosome reporter (CD63-GFP(f/f)) mice and immuno-EM/confocal image analysis, we found that neuronal CD63-GFP(+) ILVs are primarily localized in soma and dendrites, but not in axonal terminals in vitro and in vivo. Secreted neuronal exosomes contain a subset of microRNAs (miRs) that is distinct from the miR profile of neurons. These miRs, especially the neuron-specific miR-124-3p, are potentially internalized into astrocytes. MiR-124-3p further up-regulates the predominant glutamate transporter GLT1 by suppressing GLT1-inhibiting miRs. Our findings suggest a previously undescribed neuronal exosomal miR-mediated genetic regulation of astrocyte functions, potentially opening a new frontier in understanding CNS intercellular communication. |
format | Online Article Text |
id | pubmed-6742670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67426702019-09-16 Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS Men, Yuqin Yelick, Julia Jin, Shijie Tian, Yang Chiang, Ming Sum R. Higashimori, Haruki Brown, Eoin Jarvis, Rachel Yang, Yongjie Nat Commun Article Astroglia play active and diverse roles in modulating neuronal/synaptic functions in the CNS. How these astroglial functions are regulated, especially by neuronal signals, remains largely unknown. Exosomes, a major type of extracellular vesicles (EVs) that originate from endosomal intraluminal vesicles (ILVs), have emerged as a new intercellular communication process. By generating cell-type-specific ILVs/exosome reporter (CD63-GFP(f/f)) mice and immuno-EM/confocal image analysis, we found that neuronal CD63-GFP(+) ILVs are primarily localized in soma and dendrites, but not in axonal terminals in vitro and in vivo. Secreted neuronal exosomes contain a subset of microRNAs (miRs) that is distinct from the miR profile of neurons. These miRs, especially the neuron-specific miR-124-3p, are potentially internalized into astrocytes. MiR-124-3p further up-regulates the predominant glutamate transporter GLT1 by suppressing GLT1-inhibiting miRs. Our findings suggest a previously undescribed neuronal exosomal miR-mediated genetic regulation of astrocyte functions, potentially opening a new frontier in understanding CNS intercellular communication. Nature Publishing Group UK 2019-09-12 /pmc/articles/PMC6742670/ /pubmed/31515491 http://dx.doi.org/10.1038/s41467-019-11534-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Men, Yuqin Yelick, Julia Jin, Shijie Tian, Yang Chiang, Ming Sum R. Higashimori, Haruki Brown, Eoin Jarvis, Rachel Yang, Yongjie Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title | Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title_full | Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title_fullStr | Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title_full_unstemmed | Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title_short | Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS |
title_sort | exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the cns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742670/ https://www.ncbi.nlm.nih.gov/pubmed/31515491 http://dx.doi.org/10.1038/s41467-019-11534-w |
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