4.8 Article

Tracing the origin of adult intestinal stem cells

Journal

NATURE
Volume 570, Issue 7759, Pages 107-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41586-019-1212-5

Keywords

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Funding

  1. Lundbeck Foundation [R105-A9755, R190-2014-3904]
  2. Novo Nordisk Foundation [NNF14OC0012927, NNF16OC0019920, NNF17CC0027852, NNF18CC0034900]
  3. Carlsberg Foundation
  4. EMBO Young Investigator programme
  5. Marie Curie fellowship programme [625238/FP7-PEOPLE-2013-IIF, 656099/H2020-MSCA-IF-2014]
  6. Wellcome Trust [098357/Z/12/Z, 110326/Z/15/Z]
  7. Royal Society E. P. Abraham Research Professorship [RP\ R1\ 180165]
  8. European Union's Horizon 2020 research and innovation programme [STEMHEALTH ERCCoG682665, INTENS 668294]
  9. Novo Nordisk Fonden [NNF14OC0012927] Funding Source: researchfish
  10. Wellcome Trust [098357/Z/12/Z] Funding Source: researchfish
  11. Wellcome Trust [110326/Z/15/Z] Funding Source: Wellcome Trust

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Adult intestinal stem cells are located at the bottom of crypts of Lieberkuhn, where they express markers such as LGR5(1,2) and fuel the constant replenishment of the intestinal epithelium(1). Although fetal LGR5-expressing cells can give rise to adult intestinal stem cells(3,4), it remains unclear whether this population in the patterned epithelium represents unique intestinal stem-cell precursors. Here we show, using unbiased quantitative lineage-tracing approaches, biophysical modelling and intestinal transplantation, that all cells of the mouse intestinal epithelium-irrespective of their location and pattern of LGR5 expression in the fetal gut tube-contribute actively to the adult intestinal stem cell pool. Using 3D imaging, we find that during fetal development the villus undergoes gross remodelling and fission. This brings epithelial cells from the non-proliferative villus into the proliferative intervillus region, which enables them to contribute to the adult stem-cell niche. Our results demonstrate that large-scale remodelling of the intestinal wall and cell-fate specification are closely linked. Moreover, these findings provide a direct link between the observed plasticity and cellular reprogramming of differentiating cells in adult tissues following damage(5-9), revealing that stem-cell identity is an induced rather than a hardwired property.

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