| Literature DB >> 32272058 |
Yoshiko Hashikawa1, Koichi Hashikawa1, Mark A Rossi1, Marcus L Basiri2, Yuejia Liu1, Nathan L Johnston1, Omar R Ahmad1, Garret D Stuber3.
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.Entities:
Keywords: Act-seq; Habenula; HiPlex; SCENIC; Seurat; cross-species analysis; gene ontology analysis; mouse; scRNA-seq; zebrafish
Mesh:
Year: 2020 PMID: 32272058 PMCID: PMC7285796 DOI: 10.1016/j.neuron.2020.03.011
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173