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A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain

Dopamine (DA) plays a fundamental role in insect behavior as it acts both as a general modulator of behavior and as a value system in associative learning where it mediates the reinforcing properties of unconditioned stimuli (US). Here we aimed at characterizing the dopaminergic neurons in the centr...

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Autores principales: Tedjakumala, Stevanus R., Rouquette, Jacques, Boizeau, Marie-Laure, Mesce, Karen A., Hotier, Lucie, Massou, Isabelle, Giurfa, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502285/
https://www.ncbi.nlm.nih.gov/pubmed/28740466
http://dx.doi.org/10.3389/fnsys.2017.00047
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author Tedjakumala, Stevanus R.
Rouquette, Jacques
Boizeau, Marie-Laure
Mesce, Karen A.
Hotier, Lucie
Massou, Isabelle
Giurfa, Martin
author_facet Tedjakumala, Stevanus R.
Rouquette, Jacques
Boizeau, Marie-Laure
Mesce, Karen A.
Hotier, Lucie
Massou, Isabelle
Giurfa, Martin
author_sort Tedjakumala, Stevanus R.
collection PubMed
description Dopamine (DA) plays a fundamental role in insect behavior as it acts both as a general modulator of behavior and as a value system in associative learning where it mediates the reinforcing properties of unconditioned stimuli (US). Here we aimed at characterizing the dopaminergic neurons in the central nervous system of the honey bee, an insect that serves as an established model for the study of learning and memory. We used tyrosine hydroxylase (TH) immunoreactivity (ir) to ensure that the neurons detected synthesize DA endogenously. We found three main dopaminergic clusters, C1–C3, which had been previously described; the C1 cluster is located in a small region adjacent to the esophagus (ES) and the antennal lobe (AL); the C2 cluster is situated above the C1 cluster, between the AL and the vertical lobe (VL) of the mushroom body (MB); the C3 cluster is located below the calyces (CA) of the MB. In addition, we found a novel dopaminergic cluster, C4, located above the dorsomedial border of the lobula, which innervates the visual neuropils of the bee brain. Additional smaller processes and clusters were found and are described. The profuse dopaminergic innervation of the entire bee brain and the specific connectivity of DA neurons, with visual, olfactory and gustatory circuits, provide a foundation for a deeper understanding of how these sensory modules are modulated by DA, and the DA-dependent value-based associations that occur during associative learning.
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spelling pubmed-55022852017-07-24 A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain Tedjakumala, Stevanus R. Rouquette, Jacques Boizeau, Marie-Laure Mesce, Karen A. Hotier, Lucie Massou, Isabelle Giurfa, Martin Front Syst Neurosci Neuroscience Dopamine (DA) plays a fundamental role in insect behavior as it acts both as a general modulator of behavior and as a value system in associative learning where it mediates the reinforcing properties of unconditioned stimuli (US). Here we aimed at characterizing the dopaminergic neurons in the central nervous system of the honey bee, an insect that serves as an established model for the study of learning and memory. We used tyrosine hydroxylase (TH) immunoreactivity (ir) to ensure that the neurons detected synthesize DA endogenously. We found three main dopaminergic clusters, C1–C3, which had been previously described; the C1 cluster is located in a small region adjacent to the esophagus (ES) and the antennal lobe (AL); the C2 cluster is situated above the C1 cluster, between the AL and the vertical lobe (VL) of the mushroom body (MB); the C3 cluster is located below the calyces (CA) of the MB. In addition, we found a novel dopaminergic cluster, C4, located above the dorsomedial border of the lobula, which innervates the visual neuropils of the bee brain. Additional smaller processes and clusters were found and are described. The profuse dopaminergic innervation of the entire bee brain and the specific connectivity of DA neurons, with visual, olfactory and gustatory circuits, provide a foundation for a deeper understanding of how these sensory modules are modulated by DA, and the DA-dependent value-based associations that occur during associative learning. Frontiers Media S.A. 2017-07-10 /pmc/articles/PMC5502285/ /pubmed/28740466 http://dx.doi.org/10.3389/fnsys.2017.00047 Text en Copyright © 2017 Tedjakumala, Rouquette, Boizeau, Mesce, Hotier, Massou and Giurfa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Tedjakumala, Stevanus R.
Rouquette, Jacques
Boizeau, Marie-Laure
Mesce, Karen A.
Hotier, Lucie
Massou, Isabelle
Giurfa, Martin
A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title_full A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title_fullStr A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title_full_unstemmed A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title_short A Tyrosine-Hydroxylase Characterization of Dopaminergic Neurons in the Honey Bee Brain
title_sort tyrosine-hydroxylase characterization of dopaminergic neurons in the honey bee brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502285/
https://www.ncbi.nlm.nih.gov/pubmed/28740466
http://dx.doi.org/10.3389/fnsys.2017.00047
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