Single-cell transcriptomes and whole-brain projections of serotonin neurons in the mouse dorsal and median raphe nuclei

Jing Ren(Howard Hughes Medical Institute), Alina Isakova(Stanford University), Drew Friedmann(Howard Hughes Medical Institute), Jiawei Zeng(National Institute of Biological Sciences, Beijing), Sophie M. Grutzner(Howard Hughes Medical Institute), Albert Pun(Howard Hughes Medical Institute), Grace Zhao(Stanford University), Sai Saroja Kolluru(Stanford University), Ruiyu Wang(National Institute of Biological Sciences, Beijing), Rui Lin(National Institute of Biological Sciences, Beijing), Pengcheng Li(Suzhou Research Institute), Anan Li(Suzhou Research Institute), Jennifer L Raymond(Stanford University), Qingming Luo(Wuhan National Laboratory for Optoelectronics), Minmin Luo(National Institute of Biological Sciences, Beijing), Stephen R. Quake(Chan Zuckerberg Initiative (United States)), Liqun Luo(Howard Hughes Medical Institute)
eLife
October 24, 2019
Cited by 326Open Access
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Abstract

Serotonin neurons of the dorsal and median raphe nuclei (DR, MR) collectively innervate the entire forebrain and midbrain, modulating diverse physiology and behavior. To gain a fundamental understanding of their molecular heterogeneity, we used plate-based single-cell RNA-sequencing to generate a comprehensive dataset comprising eleven transcriptomically distinct serotonin neuron clusters. Systematic in situ hybridization mapped specific clusters to the principal DR, caudal DR, or MR. These transcriptomic clusters differentially express a rich repertoire of neuropeptides, receptors, ion channels, and transcription factors. We generated novel intersectional viral-genetic tools to access specific subpopulations. Whole-brain axonal projection mapping revealed that DR serotonin neurons co-expressing vesicular glutamate transporter-3 preferentially innervate the cortex, whereas those co-expressing thyrotropin-releasing hormone innervate subcortical regions in particular the hypothalamus. Reconstruction of 50 individual DR serotonin neurons revealed diverse and segregated axonal projection patterns at the single-cell level. Together, these results provide a molecular foundation of the heterogenous serotonin neuronal phenotypes.


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