Abstract

ABSTRACTThe spinal cord receives input from peripheral sensory neurons and controls motor output by regulating muscle innervating motor neurons. These functions are carried out by neural circuits comprising molecularly distinct neuronal subtypes generated in a characteristic spatiotemporal arrangement from progenitors in the embryonic neural tube. To gain insight into the diversity and complexity of cells in the developing human neural tube, we used single-cell mRNA sequencing to profile cervical and thoracic regions in four human embryos of Carnegie stages (CS) CS12, CS14, CS17 and CS19 from gestational weeks 4-7. Analysis of progenitor and neuronal populations from the neural tube and dorsal root ganglia identified dozens of distinct cell types and facilitated the reconstruction of the differentiation pathways of specific neuronal subtypes. Comparison with mouse revealed overall similarity of mammalian neural tube development while highlighting some human-specific features. These data provide a catalogue of gene expression and cell type identity in the human neural tube that will support future studies of sensory and motor control systems. The data can be explored at https://shiny.crick.ac.uk/scviewer/neuraltube/.

Highlights

  • The spinal cord receives and processes information from sensory neurons in the peripheral nervous system (PNS) and controls muscle movement by coordinating the activity of motor neurons (MNs)

  • The samples from CS12, CS14 and CS19 were processed on the same day as the termination of pregnancy, whereas CS17 was processed for sequencing after a 24 h delay

  • We applied similar quality filters to those we established for the developing mouse spinal cord (Delile et al, 2019)

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Summary

Introduction

The spinal cord receives and processes information from sensory neurons in the peripheral nervous system (PNS) and controls muscle movement by coordinating the activity of motor neurons (MNs). We generated ‘pseudo bulk RNA’ samples from the human in vivo dataset by averaging gene expression of progenitors and neurons assigned to ventral domains ( p3, pMN, p2, p1 and p0) at each time point.

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