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Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus

In the hippocampus, a functional role of dopamine D1 receptors (D1R) in synaptic plasticity and memory processes has been suggested by electrophysiological and pharmacological studies. However, comprehension of their function remains elusive due to the lack of knowledge on the precise localization o...

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Autores principales: Puighermanal, Emma, Cutando, Laura, Boubaker-Vitre, Jihane, Honoré, Eve, Longueville, Sophie, Hervé, Denis, Valjent, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406422/
https://www.ncbi.nlm.nih.gov/pubmed/27678395
http://dx.doi.org/10.1007/s00429-016-1314-x
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author Puighermanal, Emma
Cutando, Laura
Boubaker-Vitre, Jihane
Honoré, Eve
Longueville, Sophie
Hervé, Denis
Valjent, Emmanuel
author_facet Puighermanal, Emma
Cutando, Laura
Boubaker-Vitre, Jihane
Honoré, Eve
Longueville, Sophie
Hervé, Denis
Valjent, Emmanuel
author_sort Puighermanal, Emma
collection PubMed
description In the hippocampus, a functional role of dopamine D1 receptors (D1R) in synaptic plasticity and memory processes has been suggested by electrophysiological and pharmacological studies. However, comprehension of their function remains elusive due to the lack of knowledge on the precise localization of D1R expression among the diversity of interneuron populations. Using BAC transgenic mice expressing enhanced green fluorescent protein under the control of D1R promoter, we examined the molecular identity of D1R-containing neurons within the CA1 subfield of the dorsal hippocampus. In agreement with previous findings, our analysis revealed that these neurons are essentially GABAergic interneurons, which express several neurochemical markers, including calcium-binding proteins, neuropeptides, and receptors among others. Finally, by using different tools comprising cell type-specific isolation of mRNAs bound to tagged-ribosomes, we provide solid data indicating that D1R is present in a large proportion of interneurons expressing dopamine D2 receptors. Altogether, our study indicates that D1Rs are expressed by different classes of interneurons in all layers examined and not by pyramidal cells, suggesting that CA1 D1R mostly acts via modulation of GABAergic interneurons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-016-1314-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-54064222017-05-12 Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus Puighermanal, Emma Cutando, Laura Boubaker-Vitre, Jihane Honoré, Eve Longueville, Sophie Hervé, Denis Valjent, Emmanuel Brain Struct Funct Original Article In the hippocampus, a functional role of dopamine D1 receptors (D1R) in synaptic plasticity and memory processes has been suggested by electrophysiological and pharmacological studies. However, comprehension of their function remains elusive due to the lack of knowledge on the precise localization of D1R expression among the diversity of interneuron populations. Using BAC transgenic mice expressing enhanced green fluorescent protein under the control of D1R promoter, we examined the molecular identity of D1R-containing neurons within the CA1 subfield of the dorsal hippocampus. In agreement with previous findings, our analysis revealed that these neurons are essentially GABAergic interneurons, which express several neurochemical markers, including calcium-binding proteins, neuropeptides, and receptors among others. Finally, by using different tools comprising cell type-specific isolation of mRNAs bound to tagged-ribosomes, we provide solid data indicating that D1R is present in a large proportion of interneurons expressing dopamine D2 receptors. Altogether, our study indicates that D1Rs are expressed by different classes of interneurons in all layers examined and not by pyramidal cells, suggesting that CA1 D1R mostly acts via modulation of GABAergic interneurons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-016-1314-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-09-27 2017 /pmc/articles/PMC5406422/ /pubmed/27678395 http://dx.doi.org/10.1007/s00429-016-1314-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Puighermanal, Emma
Cutando, Laura
Boubaker-Vitre, Jihane
Honoré, Eve
Longueville, Sophie
Hervé, Denis
Valjent, Emmanuel
Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title_full Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title_fullStr Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title_full_unstemmed Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title_short Anatomical and molecular characterization of dopamine D1 receptor-expressing neurons of the mouse CA1 dorsal hippocampus
title_sort anatomical and molecular characterization of dopamine d1 receptor-expressing neurons of the mouse ca1 dorsal hippocampus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406422/
https://www.ncbi.nlm.nih.gov/pubmed/27678395
http://dx.doi.org/10.1007/s00429-016-1314-x
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