Human axial progenitors generate trunk neural crest cells in vitro

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Thomas Jr Frith - , University of Sheffield (Author)
  • Ilaria Granata - , High Performance Computing and Networking Institute (Author)
  • Matthew Wind - , University of Sheffield (Author)
  • Erin Stout - , University of Sheffield (Author)
  • Oliver Thompson - , University of Sheffield (Author)
  • Katrin Neumann - , Genetic Engineering of Stem Cells (Research Group), Biotechnology Center (Author)
  • Dylan Stavish - , University of Sheffield (Author)
  • Paul R Heath - , University of Sheffield (Author)
  • Daniel Ortmann - , University of Cambridge (Author)
  • James Os Hackland - , University of Sheffield (Author)
  • Konstantinos Anastassiadis - , Stem Cell Engineering (Junior Research Group), Biotechnology Center (Author)
  • Mina Gouti - , Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • James Briscoe - , The Francis Crick Institute (Author)
  • Valerie Wilson - , University of Edinburgh (Author)
  • Stuart L Johnson - , University of Sheffield (Author)
  • Marysia Placzek - , University of Sheffield (Author)
  • Mario R Guarracino - , High Performance Computing and Networking Institute (Author)
  • Peter W Andrews - , University of Sheffield (Author)
  • Anestis Tsakiridis - , University of Sheffield (Author)

Abstract

The neural crest (NC) is a multipotent embryonic cell population that generates distinct cell types in an axial position-dependent manner. The production of NC cells from human pluripotent stem cells (hPSCs) is a valuable approach to study human NC biology. However, the origin of human trunk NC remains undefined and current in vitro differentiation strategies induce only a modest yield of trunk NC cells. Here we show that hPSC-derived axial progenitors, the posteriorly-located drivers of embryonic axis elongation, give rise to trunk NC cells and their derivatives. Moreover, we define the molecular signatures associated with the emergence of human NC cells of distinct axial identities in vitro. Collectively, our findings indicate that there are two routes toward a human post-cranial NC state: the birth of cardiac and vagal NC is facilitated by retinoic acid-induced posteriorisation of an anterior precursor whereas trunk NC arises within a pool of posterior axial progenitors.

Details

Original languageEnglish
JournaleLife
Volume7
Publication statusPublished - 10 Aug 2018
Peer-reviewedYes

External IDs

PubMedCentral PMC6101942
Scopus 85053925923

Keywords

Keywords

  • Biomarkers, Cell Differentiation, Cells, Cultured, Humans, Neural Crest/physiology, Pluripotent Stem Cells/physiology