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Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval

Efficient retrieval of the synaptic vesicle (SV) membrane from the presynaptic plasma membrane, a process called endocytosis, is crucial for the fidelity of neurotransmission, particularly during sustained neural activity. Although multiple modes of endocytosis have been identified, it is clear that...

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Detalles Bibliográficos
Autores principales: Mori, Yasunori, Takamori, Shigeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770824/
https://www.ncbi.nlm.nih.gov/pubmed/29379416
http://dx.doi.org/10.3389/fncel.2017.00422
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author Mori, Yasunori
Takamori, Shigeo
author_facet Mori, Yasunori
Takamori, Shigeo
author_sort Mori, Yasunori
collection PubMed
description Efficient retrieval of the synaptic vesicle (SV) membrane from the presynaptic plasma membrane, a process called endocytosis, is crucial for the fidelity of neurotransmission, particularly during sustained neural activity. Although multiple modes of endocytosis have been identified, it is clear that the efficient retrieval of the major SV cargos into newly formed SVs during any of these modes is fundamental for synaptic transmission. It is currently believed that SVs are eventually reformed via a clathrin-dependent pathway. Various adaptor proteins recognize SV cargos and link them to clathrin, ensuring the efficient retrieval of the cargos into newly formed SVs. Here, we summarize our current knowledge of the molecular signatures within individual SV cargos that underlie efficient retrieval into SV membranes, as well as discuss possible contributions of the mechanisms under physiological conditions.
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spelling pubmed-57708242018-01-29 Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval Mori, Yasunori Takamori, Shigeo Front Cell Neurosci Neuroscience Efficient retrieval of the synaptic vesicle (SV) membrane from the presynaptic plasma membrane, a process called endocytosis, is crucial for the fidelity of neurotransmission, particularly during sustained neural activity. Although multiple modes of endocytosis have been identified, it is clear that the efficient retrieval of the major SV cargos into newly formed SVs during any of these modes is fundamental for synaptic transmission. It is currently believed that SVs are eventually reformed via a clathrin-dependent pathway. Various adaptor proteins recognize SV cargos and link them to clathrin, ensuring the efficient retrieval of the cargos into newly formed SVs. Here, we summarize our current knowledge of the molecular signatures within individual SV cargos that underlie efficient retrieval into SV membranes, as well as discuss possible contributions of the mechanisms under physiological conditions. Frontiers Media S.A. 2018-01-05 /pmc/articles/PMC5770824/ /pubmed/29379416 http://dx.doi.org/10.3389/fncel.2017.00422 Text en Copyright © 2018 Mori and Takamori. 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) or licensor 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 Neuroscience
Mori, Yasunori
Takamori, Shigeo
Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title_full Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title_fullStr Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title_full_unstemmed Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title_short Molecular Signatures Underlying Synaptic Vesicle Cargo Retrieval
title_sort molecular signatures underlying synaptic vesicle cargo retrieval
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770824/
https://www.ncbi.nlm.nih.gov/pubmed/29379416
http://dx.doi.org/10.3389/fncel.2017.00422
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