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Tracing the origin of adult intestinal stem cells.
Guiu, Jordi; Hannezo, Edouard; Yui, Shiro; Demharter, Samuel; Ulyanchenko, Svetlana; Maimets, Martti; Jørgensen, Anne; Perlman, Signe; Lundvall, Lene; Mamsen, Linn Salto; Larsen, Agnete; Olesen, Rasmus H; Andersen, Claus Yding; Thuesen, Lea Langhoff; Hare, Kristine Juul; Pers, Tune H; Khodosevich, Konstantin; Simons, Benjamin D; Jensen, Kim B.
Afiliación
  • Guiu J; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
  • Hannezo E; The Wellcome Trust-Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK.
  • Yui S; Institute of Science and Technology Austria, Klosterneuburg, Austria.
  • Demharter S; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
  • Ulyanchenko S; Center for Stem Cell and Regenerative Medicine, Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Maimets M; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
  • Jørgensen A; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
  • Perlman S; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
  • Lundvall L; Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Mamsen LS; Department of Gynecology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Larsen A; Department of Gynecology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Olesen RH; Laboratory of Reproductive Biology, Section 5712, The Juliane Marie Centre for Women, Children and Reproduction, University Hospital of Copenhagen, University of Copenhagen, Copenhagen, Denmark.
  • Andersen CY; Department of Biomedicine-Pharmacology, Aarhus University, Aarhus, Denmark.
  • Thuesen LL; Department of Biomedicine-Pharmacology, Aarhus University, Aarhus, Denmark.
  • Hare KJ; Laboratory of Reproductive Biology, Section 5712, The Juliane Marie Centre for Women, Children and Reproduction, University Hospital of Copenhagen, University of Copenhagen, Copenhagen, Denmark.
  • Pers TH; Department of Obstetrics and Gynaecology, Hvidovre University Hospital, Hvidovre, Denmark.
  • Khodosevich K; Department of Obstetrics and Gynaecology, Hvidovre University Hospital, Hvidovre, Denmark.
  • Simons BD; The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Jensen KB; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
Nature ; 570(7759): 107-111, 2019 06.
Article en En | MEDLINE | ID: mdl-31092921
ABSTRACT
Adult intestinal stem cells are located at the bottom of crypts of Lieberkühn, where they express markers such as LGR51,2 and fuel the constant replenishment of the intestinal epithelium1. Although fetal LGR5-expressing cells can give rise to adult intestinal stem cells3,4, 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 damage5-9, revealing that stem-cell identity is an induced rather than a hardwired property.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células Madre / Linaje de la Célula / Intestinos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nature Año: 2019 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células Madre / Linaje de la Célula / Intestinos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nature Año: 2019 Tipo del documento: Article País de afiliación: Dinamarca