Cargando…

Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies

Simultaneous stimulation of the antennal lobes (ALs) and the ascending fibers of the ventral nerve cord (AFV), two sensory inputs to the mushroom bodies (MBs), induces long-term enhancement (LTE) of subsequent AL-evoked MB responses. LTE induction requires activation of at least three signaling path...

Descripción completa

Detalles Bibliográficos
Autores principales: Ueno, Kohei, Suzuki, Ema, Naganos, Shintaro, Ofusa, Kyoko, Horiuchi, Junjiro, Saitoe, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262376/
https://www.ncbi.nlm.nih.gov/pubmed/28117664
http://dx.doi.org/10.7554/eLife.21076
_version_ 1782499757030113280
author Ueno, Kohei
Suzuki, Ema
Naganos, Shintaro
Ofusa, Kyoko
Horiuchi, Junjiro
Saitoe, Minoru
author_facet Ueno, Kohei
Suzuki, Ema
Naganos, Shintaro
Ofusa, Kyoko
Horiuchi, Junjiro
Saitoe, Minoru
author_sort Ueno, Kohei
collection PubMed
description Simultaneous stimulation of the antennal lobes (ALs) and the ascending fibers of the ventral nerve cord (AFV), two sensory inputs to the mushroom bodies (MBs), induces long-term enhancement (LTE) of subsequent AL-evoked MB responses. LTE induction requires activation of at least three signaling pathways to the MBs, mediated by nicotinic acetylcholine receptors (nAChRs), NMDA receptors (NRs), and D1 dopamine receptors (D1Rs). Here, we demonstrate that inputs from the AL are transmitted to the MBs through nAChRs, and inputs from the AFV are transmitted by NRs. Dopamine signaling occurs downstream of both nAChR and NR activation, and requires simultaneous stimulation of both pathways. Dopamine release requires the activity of the rutabaga adenylyl cyclase in postsynaptic MB neurons, and release is restricted to MB neurons that receive coincident stimulation. Our results indicate that postsynaptic activity can gate presynaptic dopamine release to regulate plasticity. DOI: http://dx.doi.org/10.7554/eLife.21076.001
format Online
Article
Text
id pubmed-5262376
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-52623762017-02-01 Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies Ueno, Kohei Suzuki, Ema Naganos, Shintaro Ofusa, Kyoko Horiuchi, Junjiro Saitoe, Minoru eLife Neuroscience Simultaneous stimulation of the antennal lobes (ALs) and the ascending fibers of the ventral nerve cord (AFV), two sensory inputs to the mushroom bodies (MBs), induces long-term enhancement (LTE) of subsequent AL-evoked MB responses. LTE induction requires activation of at least three signaling pathways to the MBs, mediated by nicotinic acetylcholine receptors (nAChRs), NMDA receptors (NRs), and D1 dopamine receptors (D1Rs). Here, we demonstrate that inputs from the AL are transmitted to the MBs through nAChRs, and inputs from the AFV are transmitted by NRs. Dopamine signaling occurs downstream of both nAChR and NR activation, and requires simultaneous stimulation of both pathways. Dopamine release requires the activity of the rutabaga adenylyl cyclase in postsynaptic MB neurons, and release is restricted to MB neurons that receive coincident stimulation. Our results indicate that postsynaptic activity can gate presynaptic dopamine release to regulate plasticity. DOI: http://dx.doi.org/10.7554/eLife.21076.001 eLife Sciences Publications, Ltd 2017-01-24 /pmc/articles/PMC5262376/ /pubmed/28117664 http://dx.doi.org/10.7554/eLife.21076 Text en © 2017, Ueno 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 Neuroscience
Ueno, Kohei
Suzuki, Ema
Naganos, Shintaro
Ofusa, Kyoko
Horiuchi, Junjiro
Saitoe, Minoru
Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title_full Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title_fullStr Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title_full_unstemmed Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title_short Coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in Drosophila mushroom bodies
title_sort coincident postsynaptic activity gates presynaptic dopamine release to induce plasticity in drosophila mushroom bodies
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262376/
https://www.ncbi.nlm.nih.gov/pubmed/28117664
http://dx.doi.org/10.7554/eLife.21076
work_keys_str_mv AT uenokohei coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies
AT suzukiema coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies
AT naganosshintaro coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies
AT ofusakyoko coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies
AT horiuchijunjiro coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies
AT saitoeminoru coincidentpostsynapticactivitygatespresynapticdopaminereleasetoinduceplasticityindrosophilamushroombodies