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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...

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Autores principales: Men, Yuqin, Yelick, Julia, Jin, Shijie, Tian, Yang, Chiang, Ming Sum R., Higashimori, Haruki, Brown, Eoin, Jarvis, Rachel, Yang, Yongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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