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Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning
Neurotransmitters are released at synapses by synaptic vesicles (SVs), which originate from SV precursors (SVPs) that have traveled along the axon. Because each synapse maintains a pool of SVs, only a small fraction of which are released, it has been thought that axonal transport of SVPs does not af...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365837/ https://www.ncbi.nlm.nih.gov/pubmed/37431882 http://dx.doi.org/10.7554/eLife.81011 |
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author | Vitet, Hélène Bruyère, Julie Xu, Hao Séris, Claire Brocard, Jacques Abada, Yah-Sé Delatour, Benoît Scaramuzzino, Chiara Venance, Laurent Saudou, Frédéric |
author_facet | Vitet, Hélène Bruyère, Julie Xu, Hao Séris, Claire Brocard, Jacques Abada, Yah-Sé Delatour, Benoît Scaramuzzino, Chiara Venance, Laurent Saudou, Frédéric |
author_sort | Vitet, Hélène |
collection | PubMed |
description | Neurotransmitters are released at synapses by synaptic vesicles (SVs), which originate from SV precursors (SVPs) that have traveled along the axon. Because each synapse maintains a pool of SVs, only a small fraction of which are released, it has been thought that axonal transport of SVPs does not affect synaptic function. Here, studying the corticostriatal network both in microfluidic devices and in mice, we find that phosphorylation of the Huntingtin protein (HTT) increases axonal transport of SVPs and synaptic glutamate release by recruiting the kinesin motor KIF1A. In mice, constitutive HTT phosphorylation causes SV over-accumulation at synapses, increases the probability of SV release, and impairs motor skill learning on the rotating rod. Silencing KIF1A in these mice restored SV transport and motor skill learning to wild-type levels. Axonal SVP transport within the corticostriatal network thus influences synaptic plasticity and motor skill learning. |
format | Online Article Text |
id | pubmed-10365837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-103658372023-07-25 Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning Vitet, Hélène Bruyère, Julie Xu, Hao Séris, Claire Brocard, Jacques Abada, Yah-Sé Delatour, Benoît Scaramuzzino, Chiara Venance, Laurent Saudou, Frédéric eLife Neuroscience Neurotransmitters are released at synapses by synaptic vesicles (SVs), which originate from SV precursors (SVPs) that have traveled along the axon. Because each synapse maintains a pool of SVs, only a small fraction of which are released, it has been thought that axonal transport of SVPs does not affect synaptic function. Here, studying the corticostriatal network both in microfluidic devices and in mice, we find that phosphorylation of the Huntingtin protein (HTT) increases axonal transport of SVPs and synaptic glutamate release by recruiting the kinesin motor KIF1A. In mice, constitutive HTT phosphorylation causes SV over-accumulation at synapses, increases the probability of SV release, and impairs motor skill learning on the rotating rod. Silencing KIF1A in these mice restored SV transport and motor skill learning to wild-type levels. Axonal SVP transport within the corticostriatal network thus influences synaptic plasticity and motor skill learning. eLife Sciences Publications, Ltd 2023-07-11 /pmc/articles/PMC10365837/ /pubmed/37431882 http://dx.doi.org/10.7554/eLife.81011 Text en © 2023, Vitet 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 | Neuroscience Vitet, Hélène Bruyère, Julie Xu, Hao Séris, Claire Brocard, Jacques Abada, Yah-Sé Delatour, Benoît Scaramuzzino, Chiara Venance, Laurent Saudou, Frédéric Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title | Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title_full | Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title_fullStr | Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title_full_unstemmed | Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title_short | Huntingtin recruits KIF1A to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
title_sort | huntingtin recruits kif1a to transport synaptic vesicle precursors along the mouse axon to support synaptic transmission and motor skill learning |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365837/ https://www.ncbi.nlm.nih.gov/pubmed/37431882 http://dx.doi.org/10.7554/eLife.81011 |
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