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NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety

NG2 glia, also known as oligodendrocyte precursor cells (OPCs), play an important role in proliferation and give rise to myelinating oligodendrocytes during early brain development. In contrast to other glial cell types, the most intriguing aspect of NG2 glia is their ability to directly sense synap...

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Autores principales: Zhang, Xiao, Liu, Yao, Hong, Xiaoqi, Li, Xia, Meshul, Charles K., Moore, Cynthia, Yang, Yabing, Han, Yanfei, Li, Wei-Guang, Qi, Xin, Lou, Huifang, Duan, Shumin, Xu, Tian-Le, Tong, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484468/
https://www.ncbi.nlm.nih.gov/pubmed/34593806
http://dx.doi.org/10.1038/s41467-021-25956-y
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author Zhang, Xiao
Liu, Yao
Hong, Xiaoqi
Li, Xia
Meshul, Charles K.
Moore, Cynthia
Yang, Yabing
Han, Yanfei
Li, Wei-Guang
Qi, Xin
Lou, Huifang
Duan, Shumin
Xu, Tian-Le
Tong, Xiaoping
author_facet Zhang, Xiao
Liu, Yao
Hong, Xiaoqi
Li, Xia
Meshul, Charles K.
Moore, Cynthia
Yang, Yabing
Han, Yanfei
Li, Wei-Guang
Qi, Xin
Lou, Huifang
Duan, Shumin
Xu, Tian-Le
Tong, Xiaoping
author_sort Zhang, Xiao
collection PubMed
description NG2 glia, also known as oligodendrocyte precursor cells (OPCs), play an important role in proliferation and give rise to myelinating oligodendrocytes during early brain development. In contrast to other glial cell types, the most intriguing aspect of NG2 glia is their ability to directly sense synaptic inputs from neurons. However, whether this synaptic interaction is bidirectional or unidirectional, or its physiological relevance has not yet been clarified. Here, we report that NG2 glia form synaptic complexes with hippocampal interneurons and that selective photostimulation of NG2 glia (expressing channelrhodopsin-2) functionally drives GABA release and enhances inhibitory synaptic transmission onto proximal interneurons in a microcircuit. The mechanism involves GAD67 biosynthesis and VAMP-2 containing vesicular exocytosis. Further, behavioral assays demonstrate that NG2 glia photoactivation triggers anxiety-like behavior in vivo and contributes to chronic social defeat stress.
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spelling pubmed-84844682021-10-22 NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety Zhang, Xiao Liu, Yao Hong, Xiaoqi Li, Xia Meshul, Charles K. Moore, Cynthia Yang, Yabing Han, Yanfei Li, Wei-Guang Qi, Xin Lou, Huifang Duan, Shumin Xu, Tian-Le Tong, Xiaoping Nat Commun Article NG2 glia, also known as oligodendrocyte precursor cells (OPCs), play an important role in proliferation and give rise to myelinating oligodendrocytes during early brain development. In contrast to other glial cell types, the most intriguing aspect of NG2 glia is their ability to directly sense synaptic inputs from neurons. However, whether this synaptic interaction is bidirectional or unidirectional, or its physiological relevance has not yet been clarified. Here, we report that NG2 glia form synaptic complexes with hippocampal interneurons and that selective photostimulation of NG2 glia (expressing channelrhodopsin-2) functionally drives GABA release and enhances inhibitory synaptic transmission onto proximal interneurons in a microcircuit. The mechanism involves GAD67 biosynthesis and VAMP-2 containing vesicular exocytosis. Further, behavioral assays demonstrate that NG2 glia photoactivation triggers anxiety-like behavior in vivo and contributes to chronic social defeat stress. Nature Publishing Group UK 2021-09-30 /pmc/articles/PMC8484468/ /pubmed/34593806 http://dx.doi.org/10.1038/s41467-021-25956-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Xiao
Liu, Yao
Hong, Xiaoqi
Li, Xia
Meshul, Charles K.
Moore, Cynthia
Yang, Yabing
Han, Yanfei
Li, Wei-Guang
Qi, Xin
Lou, Huifang
Duan, Shumin
Xu, Tian-Le
Tong, Xiaoping
NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title_full NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title_fullStr NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title_full_unstemmed NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title_short NG2 glia-derived GABA release tunes inhibitory synapses and contributes to stress-induced anxiety
title_sort ng2 glia-derived gaba release tunes inhibitory synapses and contributes to stress-induced anxiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484468/
https://www.ncbi.nlm.nih.gov/pubmed/34593806
http://dx.doi.org/10.1038/s41467-021-25956-y
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