| Literature DB >> 36266547 |
Lukas Steuernagel1, Brian Y H Lam2, Paul Klemm1, Georgina K C Dowsett2, Corinna A Bauder1, John A Tadross2,3,4, Tamara Sotelo Hitschfeld1, Almudena Del Rio Martin1, Weiyi Chen1, Alain J de Solis1, Henning Fenselau5,6,7, Peter Davidsen8, Irene Cimino2, Sara N Kohnke2, Debra Rimmington2, Anthony P Coll2, Andreas Beyer9,10, Giles S H Yeo11, Jens C Brüning12,13,14,15,16.
Abstract
The hypothalamus plays a key role in coordinating fundamental body functions. Despite recent progress in single-cell technologies, a unified catalog and molecular characterization of the heterogeneous cell types and, specifically, neuronal subtypes in this brain region are still lacking. Here, we present an integrated reference atlas, 'HypoMap,' of the murine hypothalamus, consisting of 384,925 cells, with the ability to incorporate new additional experiments. We validate HypoMap by comparing data collected from Smart-Seq+Fluidigm C1 and bulk RNA sequencing of selected neuronal cell types with different degrees of cellular heterogeneity. Finally, via HypoMap, we identify classes of neurons expressing glucagon-like peptide-1 receptor (Glp1r) and prepronociceptin (Pnoc), and validate them using single-molecule in situ hybridization. Collectively, HypoMap provides a unified framework for the systematic functional annotation of murine hypothalamic cell types, and it can serve as an important platform to unravel the functional organization of hypothalamic neurocircuits and to identify druggable targets for treating metabolic disorders.Entities:
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Year: 2022 PMID: 36266547 PMCID: PMC9584816 DOI: 10.1038/s42255-022-00657-y
Source DB: PubMed Journal: Nat Metab ISSN: 2522-5812