4.7 Article

Diversity of developing peripheral glia revealed by single-cell RNA sequencing

Journal

DEVELOPMENTAL CELL
Volume 56, Issue 17, Pages 2516-+

Publisher

CELL PRESS
DOI: 10.1016/j.devcel.2021.08.005

Keywords

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Funding

  1. Pussycat Foundation Helen Gurley Brown Presidential Initiative
  2. NIH [T32AG000222]
  3. HHMI Gilliam Fellowship for Advanced Study
  4. NIDCD [RO1 DC009223]
  5. NIH/NINDS [RO1 NS050674]

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The study identified differences in transcriptional profiles of glial precursors in somatosensory and auditory systems, but they ultimately undergo convergent differentiation to form molecularly uniform Schwann cells. However, satellite glial cells in somatosensory and auditory systems retain system-specific features.
The peripheral nervous system responds to a wide variety of sensory stimuli, a process that requires great neuronal diversity. These diverse neurons are closely associated with glial cells originating from the neural crest. However, the molecular nature and diversity among peripheral glia are not understood. Here, we used single-cell RNA sequencing to profile developing and mature glia from somatosensory dorsal root ganglia and auditory spiral ganglia We found that glial precursors (GPs) in these two systems differ in their transcriptional profiles. Despite their unique features, somatosensory and auditory GPs undergo convergent differentiation to generate molecularly uniform myelinating and non-myelinating Schwann cells. By contrast, somatosensory and auditory satellite glial cells retain system-specific features. Lastly, we identified a glial signature gene set, providing new insights into commonalities among glia across the nervous system. This survey of gene expression in peripheral glia constitutes a resource for understanding functions of glia across different sensory modalities.

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