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EMBO J. 2017 Oct 16;36(20):3029-3045. doi: 10.15252/embj.201696247. Epub 2017 Sep 12.

Ret receptor tyrosine kinase sustains proliferation and tissue maturation in intestinal epithelia.

Author information

1
MRC London Institute of Medical Sciences, Imperial College London, London, UK.
2
BRIC-Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen N, Denmark.
3
Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf (UKE), University of Hamburg, Hamburg, Germany.
4
Stem Cells and Regenerative Medicine, UCL Institute of Child Health, London, UK.
5
Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
6
Center for Human Genetic Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
7
The Danish Stem Cell Center (Danstem), Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
8
MRC London Institute of Medical Sciences, Imperial College London, London, UK i.miguel-aliaga@imperial.ac.uk.

Abstract

Expression of the Ret receptor tyrosine kinase is a defining feature of enteric neurons. Its importance is underscored by the effects of its mutation in Hirschsprung disease, leading to absence of gut innervation and severe gastrointestinal symptoms. We report a new and physiologically significant site of Ret expression in the intestine: the intestinal epithelium. Experiments in Drosophila indicate that Ret is expressed both by enteric neurons and adult intestinal epithelial progenitors, which require Ret to sustain their proliferation. Mechanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, modulated by Src and Fak kinases. We find that Ret is also expressed by the developing intestinal epithelium of mice, where its expression is maintained into the adult stage in a subset of enteroendocrine/enterochromaffin cells. Mouse organoid experiments point to an intrinsic role for Ret in promoting epithelial maturation and regulating Wnt signalling. Our findings reveal evolutionary conservation of the positive Ret/Wnt signalling feedback in both developmental and homeostatic contexts. They also suggest an epithelial contribution to Ret loss-of-function disorders such as Hirschsprung disease.

KEYWORDS:

Drosophila ; Ret; enteroendocrine; intestine; stem cell

PMID:
28899900
PMCID:
PMC5641678
DOI:
10.15252/embj.201696247
[Indexed for MEDLINE]
Free PMC Article

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