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

Author:

Ren Jing1ORCID,Isakova Alina23ORCID,Friedmann Drew1,Zeng Jiawei4,Grutzner Sophie M1,Pun Albert1,Zhao Grace Q5,Kolluru Sai Saroja23,Wang Ruiyu4,Lin Rui4,Li Pengcheng67,Li Anan67,Raymond Jennifer L5ORCID,Luo Qingming6ORCID,Luo Minmin48ORCID,Quake Stephen R239ORCID,Luo Liqun1ORCID

Affiliation:

1. Department of Biology and Howard Hughes Medical Institute, Stanford University, Stanford, United States

2. Department of Bioengineering, Stanford University, Stanford, United States

3. Department of Applied Physics, Stanford University, Stanford, United States

4. National Institute of Biological Science, Beijing, China

5. Department of Neurobiology, Stanford University School of Medicine, Stanford, United States

6. Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology (HUST), Wuhan, China

7. HUST-Suzhou Institute for Brainsmatics, JITRI Institute for Brainsmatics, Suzhou, China

8. School of Life Science, Tsinghua University, Beijing, China

9. Chan Zuckerberg Biohub, San Francisco, United States

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.

Funder

National Institutes of Health

National Science Foundation

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Beijing Municipal Government

NSFC

Swiss National Science Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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