Single-cell transcriptomes and whole-brain projections of serotonin neurons in the mouse dorsal and median raphe nuclei.
Jing RenAlina IsakovaDrew FriedmannJiawei ZengSophie M GrutznerAlbert PunGrace Q ZhaoSai Saroja KolluruRuiyu WangRui LinPengcheng LiAnan LiJennifer L RaymondQingming LuoMinmin LuoStephen R QuakeLiqun LuoPublished in: eLife (2019)
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.
Keyphrases
- single cell
- rna seq
- spinal cord
- editorial comment
- high throughput
- spinal cord injury
- white matter
- neuropathic pain
- transcription factor
- high resolution
- signaling pathway
- magnetic resonance
- sars cov
- computed tomography
- multiple sclerosis
- magnetic resonance imaging
- image quality
- cerebral ischemia
- single molecule
- blood brain barrier