Cargando…

NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans

Modulation of gap junction-mediated electrical synapses is a common form of neural plasticity. However, the behavioral consequence of the modulation and the underlying molecular cellular mechanisms are not understood. Here, using a C. elegans circuit of interneurons that are connected by gap junctio...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Myung-Kyu, Liu, He, Wu, Taihong, Yang, Wenxing, Zhang, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351742/
https://www.ncbi.nlm.nih.gov/pubmed/32651378
http://dx.doi.org/10.1038/s41467-020-17218-0
_version_ 1783557503646171136
author Choi, Myung-Kyu
Liu, He
Wu, Taihong
Yang, Wenxing
Zhang, Yun
author_facet Choi, Myung-Kyu
Liu, He
Wu, Taihong
Yang, Wenxing
Zhang, Yun
author_sort Choi, Myung-Kyu
collection PubMed
description Modulation of gap junction-mediated electrical synapses is a common form of neural plasticity. However, the behavioral consequence of the modulation and the underlying molecular cellular mechanisms are not understood. Here, using a C. elegans circuit of interneurons that are connected by gap junctions, we show that modulation of the gap junctions facilitates olfactory learning. Learning experience weakens the gap junctions and induces a repulsive sensory response to the training odorants, which together decouple the responses of the interneurons to the training odorants to generate learned olfactory behavior. The weakening of the gap junctions results from downregulation of the abundance of a gap junction molecule, which is regulated by cell-autonomous function of the worm homologs of a NMDAR subunit and CaMKII. Thus, our findings identify the function of a gap junction modulation in an in vivo model of learning and a conserved regulatory pathway underlying the modulation.
format Online
Article
Text
id pubmed-7351742
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-73517422020-07-13 NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans Choi, Myung-Kyu Liu, He Wu, Taihong Yang, Wenxing Zhang, Yun Nat Commun Article Modulation of gap junction-mediated electrical synapses is a common form of neural plasticity. However, the behavioral consequence of the modulation and the underlying molecular cellular mechanisms are not understood. Here, using a C. elegans circuit of interneurons that are connected by gap junctions, we show that modulation of the gap junctions facilitates olfactory learning. Learning experience weakens the gap junctions and induces a repulsive sensory response to the training odorants, which together decouple the responses of the interneurons to the training odorants to generate learned olfactory behavior. The weakening of the gap junctions results from downregulation of the abundance of a gap junction molecule, which is regulated by cell-autonomous function of the worm homologs of a NMDAR subunit and CaMKII. Thus, our findings identify the function of a gap junction modulation in an in vivo model of learning and a conserved regulatory pathway underlying the modulation. Nature Publishing Group UK 2020-07-10 /pmc/articles/PMC7351742/ /pubmed/32651378 http://dx.doi.org/10.1038/s41467-020-17218-0 Text en © The Author(s) 2020 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
Choi, Myung-Kyu
Liu, He
Wu, Taihong
Yang, Wenxing
Zhang, Yun
NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title_full NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title_fullStr NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title_full_unstemmed NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title_short NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans
title_sort nmdar-mediated modulation of gap junction circuit regulates olfactory learning in c. elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351742/
https://www.ncbi.nlm.nih.gov/pubmed/32651378
http://dx.doi.org/10.1038/s41467-020-17218-0
work_keys_str_mv AT choimyungkyu nmdarmediatedmodulationofgapjunctioncircuitregulatesolfactorylearningincelegans
AT liuhe nmdarmediatedmodulationofgapjunctioncircuitregulatesolfactorylearningincelegans
AT wutaihong nmdarmediatedmodulationofgapjunctioncircuitregulatesolfactorylearningincelegans
AT yangwenxing nmdarmediatedmodulationofgapjunctioncircuitregulatesolfactorylearningincelegans
AT zhangyun nmdarmediatedmodulationofgapjunctioncircuitregulatesolfactorylearningincelegans