1. Developmental Biology
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Generation of the squamous epithelial roof of the 4th ventricle

  1. Florent Campo-Paysaa
  2. Jonathan DW Clarke  Is a corresponding author
  3. Richard JT Wingate  Is a corresponding author
  1. King's College London, United Kingdom
Research Article
  • Cited 3
  • Views 812
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Cite this article as: eLife 2019;8:e38485 doi: 10.7554/eLife.38485

Abstract

We use the transparency of zebrafish embryos to reveal the de novo generation of a simple squamous epithelium and identify the cellular architecture in the epithelial transition zone that ties this squamous epithelium to the columnar neuroepithelium within the embryo's brain. The simple squamous epithelium of the rhombencephalic roof plate is pioneered by distinct mesenchymal cells at the dorsal midline of the neural tube. Subsequently, a progenitor zone is established at the interface between columnar epithelium of the rhombic lip and the expanding squamous epithelium of the roof plate. Surprisingly, this interface consists of a single progenitor cell type that we have named the veil cell. Veil cells express gdf6a and constitute a lineage restricted stem zone that generates the squamous roof plate by direct transformation and asymmetrically fated divisions. Experimental restriction of roof plate expansion leads to extrusion of veil cell daughters and squamous cells, suggesting veil cell fate is regulated by the space available for roof plate growth.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files

Article and author information

Author details

  1. Florent Campo-Paysaa

    Department of Developmental Neurobiology, King's College London, London, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  2. Jonathan DW Clarke

    Department of Developmental Neurobiology, King's College London, London, United Kingdom
    For correspondence
    jon.clarke@kcl.ac.uk
    Competing interests
    The authors declare that no competing interests exist.
  3. Richard JT Wingate

    Department of Developmental Neurobiology, King's College London, London, United Kingdom
    For correspondence
    richard.wingate@kcl.ac.uk
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1662-6097

Funding

Biotechnology and Biological Sciences Research Council (BB/I021507/1)

  • Jonathan DW Clarke
  • Richard JT Wingate

Wellcome

  • Jonathan DW Clarke

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Ethics

Animal experimentation: This study was performed in strict accordance with the local ethics committee of King's College London and all animals handled according to the provisions of the Home Office UK Animals Scientific Procedures act 1986 (licence P70880F4C).

Reviewing Editor

  1. Tanya T Whitfield, University of Sheffield, United Kingdom

Publication history

  1. Received: May 18, 2018
  2. Accepted: February 18, 2019
  3. Accepted Manuscript published: February 18, 2019 (version 1)
  4. Version of Record published: February 28, 2019 (version 2)

Copyright

© 2019, Campo-Paysaa et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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Further reading

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