A developmental atlas of somatosensory diversification and maturation in the dorsal root ganglia by single-cell mass cytometry

Precisely controlled development of the somatosensory system is essential for detecting pain, itch, temperature, mechanical touch and body position. To investigate the protein-level changes that occur during somatosensory development, we performed single-cell mass cytometry on dorsal root ganglia fr...

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Veröffentlicht in:Nature neuroscience 2022-11, Vol.25 (11), p.1543-1558
Hauptverfasser: Keeler, Austin B., Van Deusen, Amy L., Gadani, Irene C., Williams, Corey M., Goggin, Sarah M., Hirt, Ashley K., Vradenburgh, Shayla A., Fread, Kristen I., Puleo, Emily A., Jin, Lucy, Calhan, O. Yipkin, Deppmann, Christopher D., Zunder, Eli R.
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container_end_page 1558
container_issue 11
container_start_page 1543
container_title Nature neuroscience
container_volume 25
creator Keeler, Austin B.
Van Deusen, Amy L.
Gadani, Irene C.
Williams, Corey M.
Goggin, Sarah M.
Hirt, Ashley K.
Vradenburgh, Shayla A.
Fread, Kristen I.
Puleo, Emily A.
Jin, Lucy
Calhan, O. Yipkin
Deppmann, Christopher D.
Zunder, Eli R.
description Precisely controlled development of the somatosensory system is essential for detecting pain, itch, temperature, mechanical touch and body position. To investigate the protein-level changes that occur during somatosensory development, we performed single-cell mass cytometry on dorsal root ganglia from C57/BL6 mice of both sexes, with litter replicates collected daily from embryonic day 11.5 to postnatal day 4. Measuring nearly 3 million cells, we quantified 30 molecularly distinct somatosensory glial and 41 distinct neuronal states across all timepoints. Analysis of differentiation trajectories revealed rare cells that co-express two or more Trk receptors and over-express stem cell markers, suggesting that these neurotrophic factor receptors play a role in cell fate specification. Comparison to previous RNA-based studies identified substantial differences between many protein–mRNA pairs, demonstrating the importance of protein-level measurements to identify functional cell states. Overall, this study demonstrates that mass cytometry is a high-throughput, scalable platform to rapidly phenotype somatosensory tissues. Somatosensory neurons detect pain, temperature and touch. Keeler et al. constructed a single-cell, protein-level atlas of nearly 3 million cells from the mouse dorsal root ganglia, covering 13 days of embryonic and postnatal development.
doi_str_mv 10.1038/s41593-022-01181-8
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Animal Genetics and Genomics
Animals
Behavioral Sciences
Biological Techniques
Biomedical and Life Sciences
Biomedicine
Body temperature
Cell Differentiation
Cell fate
Cytometry
Dorsal root ganglia
Embryogenesis
Female
Ganglia
Ganglia, Spinal - physiology
Male
Maturation
Mice
mRNA
Neurobiology
Neuroglia
Neuronal-glial interactions
Neurons - physiology
Neurosciences
Neurotrophic factors
Neurotrophin receptors
Pain
Phenotypes
Proteins
Receptors
Resource
RNA, Messenger - genetics
Somatosensory system
Stem cells
Trajectory analysis
Trk receptors
title A developmental atlas of somatosensory diversification and maturation in the dorsal root ganglia by single-cell mass cytometry
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