Cargando…

Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum

Neurotransmission at dopaminergic synapses has been studied with techniques that provide high temporal resolution but cannot resolve individual synapses. To elucidate the spatial dynamics and heterogeneity of individual dopamine boutons, we developed fluorescent false neurotransmitter 200 (FFN200),...

Descripción completa

Detalles Bibliográficos
Autores principales: Pereira, Daniela B., Schmitz, Yvonne, Mészáros, József, Merchant, Paolomi, Hu, Gang, Li, Shu, Henke, Adam, Lizardi-Ortiz, José E., Karpowicz, Richard J., Morgenstern, Travis J., Sonders, Mark S., Kanter, Ellen, Rodriguez, Pamela C., Mosharov, Eugene V., Sames, Dalibor, Sulzer, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853199/
https://www.ncbi.nlm.nih.gov/pubmed/26900925
http://dx.doi.org/10.1038/nn.4252
_version_ 1782430046969921536
author Pereira, Daniela B.
Schmitz, Yvonne
Mészáros, József
Merchant, Paolomi
Hu, Gang
Li, Shu
Henke, Adam
Lizardi-Ortiz, José E.
Karpowicz, Richard J.
Morgenstern, Travis J.
Sonders, Mark S.
Kanter, Ellen
Rodriguez, Pamela C.
Mosharov, Eugene V.
Sames, Dalibor
Sulzer, David
author_facet Pereira, Daniela B.
Schmitz, Yvonne
Mészáros, József
Merchant, Paolomi
Hu, Gang
Li, Shu
Henke, Adam
Lizardi-Ortiz, José E.
Karpowicz, Richard J.
Morgenstern, Travis J.
Sonders, Mark S.
Kanter, Ellen
Rodriguez, Pamela C.
Mosharov, Eugene V.
Sames, Dalibor
Sulzer, David
author_sort Pereira, Daniela B.
collection PubMed
description Neurotransmission at dopaminergic synapses has been studied with techniques that provide high temporal resolution but cannot resolve individual synapses. To elucidate the spatial dynamics and heterogeneity of individual dopamine boutons, we developed fluorescent false neurotransmitter 200 (FFN200), a vesicular monoamine transporter 2 (VMAT2) substrate that is the first probe to selectively trace monoamine exocytosis in both neuronal cell culture and brain tissue. By monitoring electrically-evoked Ca(2+) transients with GCaMP3 and FFN200 release simultaneously, we find that only a small fraction of dopamine boutons that exhibit Ca(2+) influx engage in exocytosis, a result confirmed with activity-dependent loading of the endocytic probe FM 1-43. Thus, only a low fraction of striatal dopamine axonal sites with uptake-competent VMAT2 vesicles are capable of transmitter release. This is consistent with the presence of functionally “silent” dopamine vesicle clusters and represents a first report suggestive of presynaptically silent neuromodulatory synapses.
format Online
Article
Text
id pubmed-4853199
institution National Center for Biotechnology Information
language English
publishDate 2016
record_format MEDLINE/PubMed
spelling pubmed-48531992016-08-22 Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum Pereira, Daniela B. Schmitz, Yvonne Mészáros, József Merchant, Paolomi Hu, Gang Li, Shu Henke, Adam Lizardi-Ortiz, José E. Karpowicz, Richard J. Morgenstern, Travis J. Sonders, Mark S. Kanter, Ellen Rodriguez, Pamela C. Mosharov, Eugene V. Sames, Dalibor Sulzer, David Nat Neurosci Article Neurotransmission at dopaminergic synapses has been studied with techniques that provide high temporal resolution but cannot resolve individual synapses. To elucidate the spatial dynamics and heterogeneity of individual dopamine boutons, we developed fluorescent false neurotransmitter 200 (FFN200), a vesicular monoamine transporter 2 (VMAT2) substrate that is the first probe to selectively trace monoamine exocytosis in both neuronal cell culture and brain tissue. By monitoring electrically-evoked Ca(2+) transients with GCaMP3 and FFN200 release simultaneously, we find that only a small fraction of dopamine boutons that exhibit Ca(2+) influx engage in exocytosis, a result confirmed with activity-dependent loading of the endocytic probe FM 1-43. Thus, only a low fraction of striatal dopamine axonal sites with uptake-competent VMAT2 vesicles are capable of transmitter release. This is consistent with the presence of functionally “silent” dopamine vesicle clusters and represents a first report suggestive of presynaptically silent neuromodulatory synapses. 2016-02-22 2016-04 /pmc/articles/PMC4853199/ /pubmed/26900925 http://dx.doi.org/10.1038/nn.4252 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Pereira, Daniela B.
Schmitz, Yvonne
Mészáros, József
Merchant, Paolomi
Hu, Gang
Li, Shu
Henke, Adam
Lizardi-Ortiz, José E.
Karpowicz, Richard J.
Morgenstern, Travis J.
Sonders, Mark S.
Kanter, Ellen
Rodriguez, Pamela C.
Mosharov, Eugene V.
Sames, Dalibor
Sulzer, David
Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title_full Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title_fullStr Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title_full_unstemmed Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title_short Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
title_sort fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853199/
https://www.ncbi.nlm.nih.gov/pubmed/26900925
http://dx.doi.org/10.1038/nn.4252
work_keys_str_mv AT pereiradanielab fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT schmitzyvonne fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT meszarosjozsef fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT merchantpaolomi fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT hugang fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT lishu fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT henkeadam fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT lizardiortizjosee fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT karpowiczrichardj fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT morgensterntravisj fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT sondersmarks fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT kanterellen fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT rodriguezpamelac fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT mosharoveugenev fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT samesdalibor fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum
AT sulzerdavid fluorescentfalseneurotransmitterrevealsfunctionallysilentdopaminevesicleclustersinthestriatum