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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....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5423771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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