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The cell adhesion protein CAR is a negative regulator of synaptic transmission
The Coxsackievirus and adenovirus receptor (CAR) is essential for normal electrical conductance in the heart, but its role in the postnatal brain is largely unknown. Using brain specific CAR knockout mice (KO), we discovered an unexpected role of CAR in neuronal communication. This includes increase...
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/PMC6494904/ https://www.ncbi.nlm.nih.gov/pubmed/31043663 http://dx.doi.org/10.1038/s41598-019-43150-5 |
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author | Wrackmeyer, Uta Kaldrack, Joanna Jüttner, René Pannasch, Ulrike Gimber, Niclas Freiberg, Fabian Purfürst, Bettina Kainmueller, Dagmar Schmitz, Dietmar Haucke, Volker Rathjen, Fritz G. Gotthardt, Michael |
author_facet | Wrackmeyer, Uta Kaldrack, Joanna Jüttner, René Pannasch, Ulrike Gimber, Niclas Freiberg, Fabian Purfürst, Bettina Kainmueller, Dagmar Schmitz, Dietmar Haucke, Volker Rathjen, Fritz G. Gotthardt, Michael |
author_sort | Wrackmeyer, Uta |
collection | PubMed |
description | The Coxsackievirus and adenovirus receptor (CAR) is essential for normal electrical conductance in the heart, but its role in the postnatal brain is largely unknown. Using brain specific CAR knockout mice (KO), we discovered an unexpected role of CAR in neuronal communication. This includes increased basic synaptic transmission at hippocampal Schaffer collaterals, resistance to fatigue, and enhanced long-term potentiation. Spontaneous neurotransmitter release and speed of endocytosis are increased in KOs, accompanied by increased expression of the exocytosis associated calcium sensor synaptotagmin 2. Using proximity proteomics and binding studies, we link CAR to the exocytosis machinery as it associates with syntenin and synaptobrevin/VAMP2 at the synapse. Increased synaptic function does not cause adverse effects in KO mice, as behavior and learning are unaffected. Thus, unlike the connexin-dependent suppression of atrioventricular conduction in the cardiac knockout, communication in the CAR deficient brain is improved, suggesting a role for CAR in presynaptic processes. |
format | Online Article Text |
id | pubmed-6494904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64949042019-05-17 The cell adhesion protein CAR is a negative regulator of synaptic transmission Wrackmeyer, Uta Kaldrack, Joanna Jüttner, René Pannasch, Ulrike Gimber, Niclas Freiberg, Fabian Purfürst, Bettina Kainmueller, Dagmar Schmitz, Dietmar Haucke, Volker Rathjen, Fritz G. Gotthardt, Michael Sci Rep Article The Coxsackievirus and adenovirus receptor (CAR) is essential for normal electrical conductance in the heart, but its role in the postnatal brain is largely unknown. Using brain specific CAR knockout mice (KO), we discovered an unexpected role of CAR in neuronal communication. This includes increased basic synaptic transmission at hippocampal Schaffer collaterals, resistance to fatigue, and enhanced long-term potentiation. Spontaneous neurotransmitter release and speed of endocytosis are increased in KOs, accompanied by increased expression of the exocytosis associated calcium sensor synaptotagmin 2. Using proximity proteomics and binding studies, we link CAR to the exocytosis machinery as it associates with syntenin and synaptobrevin/VAMP2 at the synapse. Increased synaptic function does not cause adverse effects in KO mice, as behavior and learning are unaffected. Thus, unlike the connexin-dependent suppression of atrioventricular conduction in the cardiac knockout, communication in the CAR deficient brain is improved, suggesting a role for CAR in presynaptic processes. Nature Publishing Group UK 2019-05-01 /pmc/articles/PMC6494904/ /pubmed/31043663 http://dx.doi.org/10.1038/s41598-019-43150-5 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 Wrackmeyer, Uta Kaldrack, Joanna Jüttner, René Pannasch, Ulrike Gimber, Niclas Freiberg, Fabian Purfürst, Bettina Kainmueller, Dagmar Schmitz, Dietmar Haucke, Volker Rathjen, Fritz G. Gotthardt, Michael The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title | The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title_full | The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title_fullStr | The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title_full_unstemmed | The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title_short | The cell adhesion protein CAR is a negative regulator of synaptic transmission |
title_sort | cell adhesion protein car is a negative regulator of synaptic transmission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494904/ https://www.ncbi.nlm.nih.gov/pubmed/31043663 http://dx.doi.org/10.1038/s41598-019-43150-5 |
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