Molecular and Cellular Mechanisms of Synaptopathies

Synapses, contact points between neurons, are essential elements supporting the ability of neurons to communicate and to transmit relevant information to each other. They play an integral role in brain development and wiring neurons into neural circuits, for example, those related to our behavior. T...

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Authors: Ardiles, Álvaro O.; Grabrucker, Andreas M.; Gómez Scholl, Francisco Manuel; Rudenko, Gabby; Borsello, Tiziana
Format: Article
Status:Published version
Publication date:2017
Country:España
Institution:Universidad de Sevilla (US)
Repository:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/161759
Online Access:https://hdl.handle.net/11441/161759
https://doi.org/10.1155/2017/2643943
Access Level:Open access
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author Ardiles, Álvaro O.
author2 Grabrucker, Andreas M.
Gómez Scholl, Francisco Manuel
Rudenko, Gabby
Borsello, Tiziana
author2_role author
author
author
author
author_browse Ardiles, Álvaro O.
Borsello, Tiziana
Grabrucker, Andreas M.
Gómez Scholl, Francisco Manuel
Rudenko, Gabby
author_facet Ardiles, Álvaro O.
Grabrucker, Andreas M.
Gómez Scholl, Francisco Manuel
Rudenko, Gabby
Borsello, Tiziana
author_role author
collection idUS. Depósito de Investigación de la Universidad de Sevilla
description Synapses, contact points between neurons, are essential elements supporting the ability of neurons to communicate and to transmit relevant information to each other. They play an integral role in brain development and wiring neurons into neural circuits, for example, those related to our behavior. Therefore, alterations affecting the integrity and/or functionality of synapses can lead to synaptic pathologies or synaptopathies. For instance, many neurological disorders including Alzheimer’s disease, Down syndrome, epilepsy, and Parkinson’s disease and neurodevelopmental disorders such as autism spectrum disorders, intellectual disability, and fragile X syndrome have consistently been reported to exhibit abnormalities in synaptic composition, morphology, and function. This special issue discusses various aspects of the molecular interactions that underlie synaptic protein networks and the complex signaling pathways that are activated by them, knowledge that is crucial to understand the cellular and molecular mechanisms involved in different synaptopathies. Synapses comprise a presynaptic compartment, consisting of the axon terminal and their protein machinery implicated in the release of neurotransmitters. Upon exocytosis of presynaptic vesicles, neurotransmitters spill out into the extracellular space called the “synaptic cleft” and diffuse to reach a postsynaptic compartment, composed of the protein machinery that receives and transduces the neurotransmitter-induced signals [1]. Most synaptopathies directly or indirectly affect the molecular repertoire of synaptic proteins.
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instname_str Universidad de Sevilla (US)
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network_name_str España
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publishDate 2017
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reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
spelling Molecular and Cellular Mechanisms of Synaptopathies Ardiles, Álvaro O. Grabrucker, Andreas M. Gómez Scholl, Francisco Manuel Rudenko, Gabby Borsello, Tiziana Synapses, contact points between neurons, are essential elements supporting the ability of neurons to communicate and to transmit relevant information to each other. They play an integral role in brain development and wiring neurons into neural circuits, for example, those related to our behavior. Therefore, alterations affecting the integrity and/or functionality of synapses can lead to synaptic pathologies or synaptopathies. For instance, many neurological disorders including Alzheimer’s disease, Down syndrome, epilepsy, and Parkinson’s disease and neurodevelopmental disorders such as autism spectrum disorders, intellectual disability, and fragile X syndrome have consistently been reported to exhibit abnormalities in synaptic composition, morphology, and function. This special issue discusses various aspects of the molecular interactions that underlie synaptic protein networks and the complex signaling pathways that are activated by them, knowledge that is crucial to understand the cellular and molecular mechanisms involved in different synaptopathies. Synapses comprise a presynaptic compartment, consisting of the axon terminal and their protein machinery implicated in the release of neurotransmitters. Upon exocytosis of presynaptic vesicles, neurotransmitters spill out into the extracellular space called the “synaptic cleft” and diffuse to reach a postsynaptic compartment, composed of the protein machinery that receives and transduces the neurotransmitter-induced signals [1]. Most synaptopathies directly or indirectly affect the molecular repertoire of synaptic proteins. Wiley Open Access https://hdl.handle.net/11441/161759 https://doi.org/10.1155/2017/2643943
spellingShingle Molecular and Cellular Mechanisms of Synaptopathies
Ardiles, Álvaro O.
status_str publishedVersion
title Molecular and Cellular Mechanisms of Synaptopathies
title_full Molecular and Cellular Mechanisms of Synaptopathies
title_fullStr Molecular and Cellular Mechanisms of Synaptopathies
title_full_unstemmed Molecular and Cellular Mechanisms of Synaptopathies
title_short Molecular and Cellular Mechanisms of Synaptopathies
title_sort Molecular and Cellular Mechanisms of Synaptopathies
url https://hdl.handle.net/11441/161759
https://doi.org/10.1155/2017/2643943