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Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy

Chemical synapses are specialized interfaces between neurons in the brain that transmit and modulate information, thereby integrating cells into multiplicity of interacting neural circuits. Cell adhesion molecules (CAMs) might form trans-synaptic complexes that are crucial for the appropriate identi...

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Detalles Bibliográficos
Autores principales: Gorlewicz, Adam, Kaczmarek, Leszek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160742/
https://www.ncbi.nlm.nih.gov/pubmed/30298130
http://dx.doi.org/10.3389/fcell.2018.00119
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author Gorlewicz, Adam
Kaczmarek, Leszek
author_facet Gorlewicz, Adam
Kaczmarek, Leszek
author_sort Gorlewicz, Adam
collection PubMed
description Chemical synapses are specialized interfaces between neurons in the brain that transmit and modulate information, thereby integrating cells into multiplicity of interacting neural circuits. Cell adhesion molecules (CAMs) might form trans-synaptic complexes that are crucial for the appropriate identification of synaptic partners and further for the establishment, properties, and dynamics of synapses. When affected, trans-synaptic adhesion mechanisms play a role in synaptopathies in a variety of neuropsychiatric disorders including epilepsy. This review recapitulates current understanding of trans-synaptic interactions in pathophysiology of interneuronal connections. In particular, we discuss here the possible implications of trans-synaptic adhesion dysfunction for epilepsy.
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spelling pubmed-61607422018-10-08 Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy Gorlewicz, Adam Kaczmarek, Leszek Front Cell Dev Biol Physiology Chemical synapses are specialized interfaces between neurons in the brain that transmit and modulate information, thereby integrating cells into multiplicity of interacting neural circuits. Cell adhesion molecules (CAMs) might form trans-synaptic complexes that are crucial for the appropriate identification of synaptic partners and further for the establishment, properties, and dynamics of synapses. When affected, trans-synaptic adhesion mechanisms play a role in synaptopathies in a variety of neuropsychiatric disorders including epilepsy. This review recapitulates current understanding of trans-synaptic interactions in pathophysiology of interneuronal connections. In particular, we discuss here the possible implications of trans-synaptic adhesion dysfunction for epilepsy. Frontiers Media S.A. 2018-09-21 /pmc/articles/PMC6160742/ /pubmed/30298130 http://dx.doi.org/10.3389/fcell.2018.00119 Text en Copyright © 2018 Gorlewicz and Kaczmarek. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Gorlewicz, Adam
Kaczmarek, Leszek
Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title_full Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title_fullStr Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title_full_unstemmed Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title_short Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
title_sort pathophysiology of trans-synaptic adhesion molecules: implications for epilepsy
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160742/
https://www.ncbi.nlm.nih.gov/pubmed/30298130
http://dx.doi.org/10.3389/fcell.2018.00119
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