Cited by 167Single-cell and spatial transcriptomicsNeuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

Transcriptional and spatial resolution of cell types in the mammalian habenula

Open access
Hashikawa, Yoshiko, Hashikawa, Koichi, Rossi, Mark A., Basiri, Marcus L., Liu, Yuejia, Johnston, Nathan L., Ahmad, Omar R., Stuber, Garret D.·2020·Neuron

Published version of a preprint

Abstract

The habenula complex is appreciated as a critical regulator of motivated and pathological behavioral states via its output to midbrain nuclei. Despite this, transcriptional definition of cell populations that comprise both the medial habenular (MHb) and lateral habenular (LHb) subregions in mammals remain undefined. To resolve this, we performed single-cell transcriptional profiling and highly multiplexed in situ hybridization experiments of the mouse habenula complex in naive mice and those exposed to an acute aversive stimulus. Transcriptionally distinct neuronal cell types identified within the MHb and LHb, were spatially defined, differentially engaged by aversive stimuli, and had distinct electrophysiological properties. Cell types identified in mice also displayed a high degree of transcriptional similarity to those previously described in zebrafish, highlighting the well-conserved nature of habenular cell types across the phylum. These data identify key molecular targets within habenular cell types and provide a critical resource for future studies.

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Crossref · 10.1016/j.neuron.2020.03.011

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  • Single-cell sequencing and ISH confirmed that these medial habenula neurons reside in the ventral and ventrolateral subregion and form a genetically distinct subtype.

    “Single-cell sequencing and in-situ hybridization (ISH) studies confirmed that these neurons reside in the ventral and ventrolateral subregion of the mHb and form a genet-ically distinct subtype.58,59”

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References 113 · Cited by 167

Authors
Hashikawa, Y., Hashikawa, K., Rossi, M. A., Basiri, M. L., Liu, Y., Johnston, N. L., Ahmad, O. R., & Stuber, G. D.
Affiliations
  • University of Washington (US)
  • University of North Carolina at Chapel Hill (US)
Corresponding author
Stuber, Garret D.
Venue
Neuron
Publisher
Elsevier BV
Published
2020-06
Volume
106
Issue
5
Pages
743-758.e5
ISSN
0896-6273 (ISSN-L)
OpenAlex
W3015690562
Cited by
167
References
113
Citations by year
2026: 23 · 2025: 28 · 2024: 32 · 2023: 20 · 2022: 30 · 2021: 19 · 2020: 14 · 2019: 1
FWCI
6.81
Type
journal article
Language
en
Open access
Locations
  • Neuron (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
  • UNC Libraries
Funders
  • National Institutes of Health (DA032750, DA038168, DK121883, NS007431)
  • Brain and Behavior Research Foundation
  • National Alliance for Research on Schizophrenia and Depression
  • Foundation of Hope for Research and Treatment of Mental Illness (P30DA048736)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
medial habenula, lateral habenula, single-cell transcriptomics, in situ hybridization, aversive stimuli, zebrafish, electrophysiological properties, motivated behavior
MeSH terms
RNA-Seq, Animals, Astrocytes, Neuroglia, Neurons, Oligodendroglia, Zebrafish, Microglia, Habenula, Gene Expression Profiling, Endothelial Cells, Mice, Single-Cell Analysis, Ependymoglial Cells, Gene Ontology

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