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      Chronic inflammation imposes aberrant cell fate in regenerating epithelia via mechanotransduction

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          Abstract

          Chronic inflammation is associated with a variety of pathological conditions in epithelial tissues, including cancer, metaplasia and aberrant wound healing. In relation to this, a significant body of evidence suggests that aberration of epithelial stem and progenitor cell function is a contributing factor in inflammation related disease, although the underlying cellular and molecular mechanisms remain to be fully elucidated. In this study, we have delineated the effect of chronic inflammation on epithelial stem/progenitor cells using the corneal epithelium as a model tissue. Using a combination of mouse genetics, pharmacological approaches and in vitro assays, we demonstrate that chronic inflammation elicits aberrant mechanotransduction in the regenerating corneal epithelium. As a consequence, a YAP-TAZ/β-catenin cascade is triggered, resulting in the induction of epidermal differentiation on the ocular surface. Collectively, this study demonstrates that chronic inflammation and mechanotransduction are linked and act to elicit pathological responses in regenerating epithelia.

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          Author and article information

          Journal
          100890575
          21417
          Nat Cell Biol
          Nat. Cell Biol.
          Nature cell biology
          1465-7392
          1476-4679
          11 October 2018
          21 December 2015
          February 2016
          19 October 2018
          : 18
          : 2
          : 168-180
          Affiliations
          [1 ]Swiss Institute for Experimental Cancer Research (ISREC), Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne, Switzerland, 1015
          [2 ]Laboratory for Bio- and Nano-Instrumentation (LBNI), Institute of Bioengineering (IBI), EPFL, Lausanne, Switzerland, 1015
          [3 ]University of Padua, Dept. Molecular Medicine, via G. Colombo 3, 35131 Padova, Italy
          [4 ]Laboratory of Stem Cell Bioengineering (LSCB), IBI, EPFL, Lausanne, Switzerland, 1015
          [5 ]Genes, Development, and Disease Group, F-BBVA Cancer Cell Biology Programme, National Cancer Research Centre (CNIO), 28029 Madrid, Spain
          [6 ]Stem Cell Dynamics Laboratory (LDSC), IBI, EPFL, Lausanne, Switzerland, 1015
          Author notes
          Correspondence and request for materials should be addressed to F.R. ( freddy.radtke@ 123456epfl.ch ) or C.S.N. ( craigscott.nowell@ 123456epfl.ch ).
          [7]

          Current address: United Kingdom Stem Cell Bank (UKSCB), National Institute for Biological Standards and Control (NIBSC), Blanche Lane, South Mimms, Hertfordshire, United Kingdom, EN6 3QG

          Article
          PMC6195194 PMC6195194 6195194 ems80066
          10.1038/ncb3290
          6195194
          26689676
          e68971d9-6c41-44fc-8c76-ca1bc226dce7
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