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Electrical synaptic transmission requires a postsynaptic scaffolding protein
Electrical synaptic transmission relies on neuronal gap junctions containing channels constructed by Connexins. While at chemical synapses neurotransmitter-gated ion channels are critically supported by scaffolding proteins, it is unknown if channels at electrical synapses require similar scaffold s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081524/ https://www.ncbi.nlm.nih.gov/pubmed/33908867 http://dx.doi.org/10.7554/eLife.66898 |
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author | Lasseigne, Abagael M Echeverry, Fabio A Ijaz, Sundas Michel, Jennifer Carlisle Martin, E Anne Marsh, Audrey J Trujillo, Elisa Marsden, Kurt C Pereda, Alberto E Miller, Adam C |
author_facet | Lasseigne, Abagael M Echeverry, Fabio A Ijaz, Sundas Michel, Jennifer Carlisle Martin, E Anne Marsh, Audrey J Trujillo, Elisa Marsden, Kurt C Pereda, Alberto E Miller, Adam C |
author_sort | Lasseigne, Abagael M |
collection | PubMed |
description | Electrical synaptic transmission relies on neuronal gap junctions containing channels constructed by Connexins. While at chemical synapses neurotransmitter-gated ion channels are critically supported by scaffolding proteins, it is unknown if channels at electrical synapses require similar scaffold support. Here, we investigated the functional relationship between neuronal Connexins and Zonula Occludens 1 (ZO1), an intracellular scaffolding protein localized to electrical synapses. Using model electrical synapses in zebrafish Mauthner cells, we demonstrated that ZO1 is required for robust synaptic Connexin localization, but Connexins are dispensable for ZO1 localization. Disrupting this hierarchical ZO1/Connexin relationship abolishes electrical transmission and disrupts Mauthner cell-initiated escape responses. We found that ZO1 is asymmetrically localized exclusively postsynaptically at neuronal contacts where it functions to assemble intercellular channels. Thus, forming functional neuronal gap junctions requires a postsynaptic scaffolding protein. The critical function of a scaffolding molecule reveals an unanticipated complexity of molecular and functional organization at electrical synapses. |
format | Online Article Text |
id | pubmed-8081524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80815242021-04-30 Electrical synaptic transmission requires a postsynaptic scaffolding protein Lasseigne, Abagael M Echeverry, Fabio A Ijaz, Sundas Michel, Jennifer Carlisle Martin, E Anne Marsh, Audrey J Trujillo, Elisa Marsden, Kurt C Pereda, Alberto E Miller, Adam C eLife Developmental Biology Electrical synaptic transmission relies on neuronal gap junctions containing channels constructed by Connexins. While at chemical synapses neurotransmitter-gated ion channels are critically supported by scaffolding proteins, it is unknown if channels at electrical synapses require similar scaffold support. Here, we investigated the functional relationship between neuronal Connexins and Zonula Occludens 1 (ZO1), an intracellular scaffolding protein localized to electrical synapses. Using model electrical synapses in zebrafish Mauthner cells, we demonstrated that ZO1 is required for robust synaptic Connexin localization, but Connexins are dispensable for ZO1 localization. Disrupting this hierarchical ZO1/Connexin relationship abolishes electrical transmission and disrupts Mauthner cell-initiated escape responses. We found that ZO1 is asymmetrically localized exclusively postsynaptically at neuronal contacts where it functions to assemble intercellular channels. Thus, forming functional neuronal gap junctions requires a postsynaptic scaffolding protein. The critical function of a scaffolding molecule reveals an unanticipated complexity of molecular and functional organization at electrical synapses. eLife Sciences Publications, Ltd 2021-04-28 /pmc/articles/PMC8081524/ /pubmed/33908867 http://dx.doi.org/10.7554/eLife.66898 Text en © 2021, Lasseigne et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Lasseigne, Abagael M Echeverry, Fabio A Ijaz, Sundas Michel, Jennifer Carlisle Martin, E Anne Marsh, Audrey J Trujillo, Elisa Marsden, Kurt C Pereda, Alberto E Miller, Adam C Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title | Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title_full | Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title_fullStr | Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title_full_unstemmed | Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title_short | Electrical synaptic transmission requires a postsynaptic scaffolding protein |
title_sort | electrical synaptic transmission requires a postsynaptic scaffolding protein |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081524/ https://www.ncbi.nlm.nih.gov/pubmed/33908867 http://dx.doi.org/10.7554/eLife.66898 |
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