Molecular and anatomical organization of the dorsal raphe nucleus

The dorsal raphe nucleus (DRN) is an important source of neuromodulators and has been implicated in a wide variety of behavioral and neurological disorders. The DRN is subdivided into distinct anatomical subregions comprised of multiple cell types, and its complex cellular organization has impeded e...

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Main Authors: Kee Wui Huang, Nicole E Ochandarena, Adrienne C Philson, Minsuk Hyun, Jaclyn E Birnbaum, Marcelo Cicconet, Bernardo L Sabatini
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/46464
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author Kee Wui Huang
Nicole E Ochandarena
Adrienne C Philson
Minsuk Hyun
Jaclyn E Birnbaum
Marcelo Cicconet
Bernardo L Sabatini
author_facet Kee Wui Huang
Nicole E Ochandarena
Adrienne C Philson
Minsuk Hyun
Jaclyn E Birnbaum
Marcelo Cicconet
Bernardo L Sabatini
author_sort Kee Wui Huang
collection DOAJ
description The dorsal raphe nucleus (DRN) is an important source of neuromodulators and has been implicated in a wide variety of behavioral and neurological disorders. The DRN is subdivided into distinct anatomical subregions comprised of multiple cell types, and its complex cellular organization has impeded efforts to investigate the distinct circuit and behavioral functions of its subdomains. Here we used single-cell RNA sequencing, in situ hybridization, anatomical tracing, and spatial correlation analysis to map the transcriptional and spatial profiles of cells from the mouse DRN. Our analysis of 39,411 single-cell transcriptomes revealed at least 18 distinct neuron subtypes and 5 serotonergic neuron subtypes with distinct molecular and anatomical properties, including a serotonergic neuron subtype that preferentially innervates the basal ganglia. Our study lays out the molecular organization of distinct serotonergic and non-serotonergic subsystems, and will facilitate the design of strategies for further dissection of the DRN and its diverse functions.
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spelling doaj.art-c50ce8c2d8a44385ab2c694c9b35011d2022-12-22T03:24:40ZengeLife Sciences Publications LtdeLife2050-084X2019-08-01810.7554/eLife.46464Molecular and anatomical organization of the dorsal raphe nucleusKee Wui Huang0https://orcid.org/0000-0003-2265-4550Nicole E Ochandarena1Adrienne C Philson2Minsuk Hyun3Jaclyn E Birnbaum4Marcelo Cicconet5Bernardo L Sabatini6https://orcid.org/0000-0003-0095-9177Department of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesImage and Data Analysis Core, Harvard Medical School, Boston, United StatesDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United StatesThe dorsal raphe nucleus (DRN) is an important source of neuromodulators and has been implicated in a wide variety of behavioral and neurological disorders. The DRN is subdivided into distinct anatomical subregions comprised of multiple cell types, and its complex cellular organization has impeded efforts to investigate the distinct circuit and behavioral functions of its subdomains. Here we used single-cell RNA sequencing, in situ hybridization, anatomical tracing, and spatial correlation analysis to map the transcriptional and spatial profiles of cells from the mouse DRN. Our analysis of 39,411 single-cell transcriptomes revealed at least 18 distinct neuron subtypes and 5 serotonergic neuron subtypes with distinct molecular and anatomical properties, including a serotonergic neuron subtype that preferentially innervates the basal ganglia. Our study lays out the molecular organization of distinct serotonergic and non-serotonergic subsystems, and will facilitate the design of strategies for further dissection of the DRN and its diverse functions.https://elifesciences.org/articles/46464dorsal raphe nucleussingle cell RNAseqserotoninneuromodulation
spellingShingle Kee Wui Huang
Nicole E Ochandarena
Adrienne C Philson
Minsuk Hyun
Jaclyn E Birnbaum
Marcelo Cicconet
Bernardo L Sabatini
Molecular and anatomical organization of the dorsal raphe nucleus
eLife
dorsal raphe nucleus
single cell RNAseq
serotonin
neuromodulation
title Molecular and anatomical organization of the dorsal raphe nucleus
title_full Molecular and anatomical organization of the dorsal raphe nucleus
title_fullStr Molecular and anatomical organization of the dorsal raphe nucleus
title_full_unstemmed Molecular and anatomical organization of the dorsal raphe nucleus
title_short Molecular and anatomical organization of the dorsal raphe nucleus
title_sort molecular and anatomical organization of the dorsal raphe nucleus
topic dorsal raphe nucleus
single cell RNAseq
serotonin
neuromodulation
url https://elifesciences.org/articles/46464
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