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Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses

Transport of synaptic vesicles (SVs) in nerve terminals is thought to play essential roles in maintenance of neurotransmission. To identify factors modulating SV movements, we performed real-time imaging analysis of fluorescently labeled SVs in giant calyceal and conventional hippocampal terminals....

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Detalles Bibliográficos
Autores principales: Guillaud, Laurent, Dimitrov, Dimitar, Takahashi, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423771/
https://www.ncbi.nlm.nih.gov/pubmed/28432787
http://dx.doi.org/10.7554/eLife.24845
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author Guillaud, Laurent
Dimitrov, Dimitar
Takahashi, Tomoyuki
author_facet Guillaud, Laurent
Dimitrov, Dimitar
Takahashi, Tomoyuki
author_sort Guillaud, Laurent
collection PubMed
description Transport of synaptic vesicles (SVs) in nerve terminals is thought to play essential roles in maintenance of neurotransmission. To identify factors modulating SV movements, we performed real-time imaging analysis of fluorescently labeled SVs in giant calyceal and conventional hippocampal terminals. Compared with small hippocampal terminals, SV movements in giant calyceal terminals were faster, longer and kinetically more heterogeneous. Morphological maturation of giant calyceal terminals was associated with an overall reduction in SV mobility and displacement heterogeneity. At the molecular level, SVs over-expressing vesicular glutamate transporter 1 (VGLUT1) showed higher mobility than VGLUT2-expressing SVs. Pharmacological disruption of the presynaptic microtubule network preferentially reduced long directional movements of SVs between release sites. Functionally, synaptic stimulation appeared to recruit SVs to active zones without significantly altering their mobility. Hence, the morphological features of nerve terminals and the molecular signature of vesicles are key elements determining vesicular dynamics and movements in central synapses. DOI: http://dx.doi.org/10.7554/eLife.24845.001
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spelling pubmed-54237712017-05-10 Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses Guillaud, Laurent Dimitrov, Dimitar Takahashi, Tomoyuki eLife Cell Biology Transport of synaptic vesicles (SVs) in nerve terminals is thought to play essential roles in maintenance of neurotransmission. To identify factors modulating SV movements, we performed real-time imaging analysis of fluorescently labeled SVs in giant calyceal and conventional hippocampal terminals. Compared with small hippocampal terminals, SV movements in giant calyceal terminals were faster, longer and kinetically more heterogeneous. Morphological maturation of giant calyceal terminals was associated with an overall reduction in SV mobility and displacement heterogeneity. At the molecular level, SVs over-expressing vesicular glutamate transporter 1 (VGLUT1) showed higher mobility than VGLUT2-expressing SVs. Pharmacological disruption of the presynaptic microtubule network preferentially reduced long directional movements of SVs between release sites. Functionally, synaptic stimulation appeared to recruit SVs to active zones without significantly altering their mobility. Hence, the morphological features of nerve terminals and the molecular signature of vesicles are key elements determining vesicular dynamics and movements in central synapses. DOI: http://dx.doi.org/10.7554/eLife.24845.001 eLife Sciences Publications, Ltd 2017-04-22 /pmc/articles/PMC5423771/ /pubmed/28432787 http://dx.doi.org/10.7554/eLife.24845 Text en © 2017, Guillaud et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Guillaud, Laurent
Dimitrov, Dimitar
Takahashi, Tomoyuki
Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title_full Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title_fullStr Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title_full_unstemmed Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title_short Presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
title_sort presynaptic morphology and vesicular composition determine vesicle dynamics in mouse central synapses
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423771/
https://www.ncbi.nlm.nih.gov/pubmed/28432787
http://dx.doi.org/10.7554/eLife.24845
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