drd2-cre:ribotag mouse line unravels the possible diversity of dopamine d2 receptor-expressing cells of the dorsal mouse hippocampus

ABSTRACT Increasing evidences suggest that dopamine facilitates the encoding of novel memories by the hippocampus. However, the role of dopamine D2 receptors (D2R) in such regulations remains elusive due to the lack of the precise identification of hippocampal D2R‐expressing cells. To address this i...

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Veröffentlicht in:Hippocampus 2015-07, Vol.25 (7), p.858-875
Hauptverfasser: Puighermanal, Emma, Biever, Anne, Espallergues, Julie, Gangarossa, Giuseppe, De Bundel, Dimitri, Valjent, Emmanuel
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container_end_page 875
container_issue 7
container_start_page 858
container_title Hippocampus
container_volume 25
creator Puighermanal, Emma
Biever, Anne
Espallergues, Julie
Gangarossa, Giuseppe
De Bundel, Dimitri
Valjent, Emmanuel
description ABSTRACT Increasing evidences suggest that dopamine facilitates the encoding of novel memories by the hippocampus. However, the role of dopamine D2 receptors (D2R) in such regulations remains elusive due to the lack of the precise identification of hippocampal D2R‐expressing cells. To address this issue, mice expressing the ribosomal protein Rpl22 tagged with the hemagglutinin (HA) epitope were crossed with Drd2‐Cre mice allowing the selective expression of HA in D2R‐containing cells (Drd2‐Cre:RiboTag mice). This new transgenic model revealed a more widespread pattern of D2R‐expressing cells identified by HA immunoreactivity than the one initially reported in Drd2‐EGFP mice, in which the hilar mossy cells were the main neuronal population detectable. In Drd2‐Cre:RiboTag mice, scattered HA/GAD67‐positive neurons were detected throughout the CA1/CA3 subfields, being preferentially localized in stratum oriens and stratum lacunosum‐moleculare. At the cellular level, HA‐labeled cells located in CA1/CA3 subfields co‐localized with calcium‐binding proteins (parvalbumin, calbindin, and calretinin), neuropeptides (neuropeptide Y, somatostatin), and other markers (neuronal nitric oxide synthase, mGluR1α, reelin, coupTFII, and potassium channel‐interacting protein 1). These results suggest that in addition to the glutamatergic hilar mossy cells, D2R‐expressing cells constitute a subpopulation of GABAergic hippocampal interneurons. © 2014 Wiley Periodicals, Inc.
doi_str_mv 10.1002/hipo.22408
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However, the role of dopamine D2 receptors (D2R) in such regulations remains elusive due to the lack of the precise identification of hippocampal D2R‐expressing cells. To address this issue, mice expressing the ribosomal protein Rpl22 tagged with the hemagglutinin (HA) epitope were crossed with Drd2‐Cre mice allowing the selective expression of HA in D2R‐containing cells (Drd2‐Cre:RiboTag mice). This new transgenic model revealed a more widespread pattern of D2R‐expressing cells identified by HA immunoreactivity than the one initially reported in Drd2‐EGFP mice, in which the hilar mossy cells were the main neuronal population detectable. In Drd2‐Cre:RiboTag mice, scattered HA/GAD67‐positive neurons were detected throughout the CA1/CA3 subfields, being preferentially localized in stratum oriens and stratum lacunosum‐moleculare. At the cellular level, HA‐labeled cells located in CA1/CA3 subfields co‐localized with calcium‐binding proteins (parvalbumin, calbindin, and calretinin), neuropeptides (neuropeptide Y, somatostatin), and other markers (neuronal nitric oxide synthase, mGluR1α, reelin, coupTFII, and potassium channel‐interacting protein 1). 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At the cellular level, HA‐labeled cells located in CA1/CA3 subfields co‐localized with calcium‐binding proteins (parvalbumin, calbindin, and calretinin), neuropeptides (neuropeptide Y, somatostatin), and other markers (neuronal nitric oxide synthase, mGluR1α, reelin, coupTFII, and potassium channel‐interacting protein 1). 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However, the role of dopamine D2 receptors (D2R) in such regulations remains elusive due to the lack of the precise identification of hippocampal D2R‐expressing cells. To address this issue, mice expressing the ribosomal protein Rpl22 tagged with the hemagglutinin (HA) epitope were crossed with Drd2‐Cre mice allowing the selective expression of HA in D2R‐containing cells (Drd2‐Cre:RiboTag mice). This new transgenic model revealed a more widespread pattern of D2R‐expressing cells identified by HA immunoreactivity than the one initially reported in Drd2‐EGFP mice, in which the hilar mossy cells were the main neuronal population detectable. In Drd2‐Cre:RiboTag mice, scattered HA/GAD67‐positive neurons were detected throughout the CA1/CA3 subfields, being preferentially localized in stratum oriens and stratum lacunosum‐moleculare. 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subjects Animals
Calbindin 2 - metabolism
Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism
Channelrhodopsins
dopamine D2 receptor
Gene Expression Regulation - genetics
Glutamate Decarboxylase - metabolism
Green Fluorescent Proteins - genetics
Green Fluorescent Proteins - metabolism
hilar mossy cells
Hippocampus - cytology
interneurons
KChIP1
Life Sciences
Male
Membrane Proteins - metabolism
Mice
Mice, Inbred C57BL
Mice, Transgenic
Microscopy, Confocal
Nerve Tissue Proteins - metabolism
Neurons - metabolism
Receptors, Dopamine D2 - genetics
Receptors, Dopamine D2 - metabolism
Ribosomal Proteins - genetics
Ribosomal Proteins - metabolism
RiboTag mice
RNA-Binding Proteins - genetics
RNA-Binding Proteins - metabolism
title drd2-cre:ribotag mouse line unravels the possible diversity of dopamine d2 receptor-expressing cells of the dorsal mouse hippocampus
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