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      Atg14 protects the intestinal epithelium from TNF-triggered villus atrophy

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          ABSTRACT

          Regulation of intestinal epithelial turnover is a key component of villus maintenance in the intestine. The balance of cell turnover can be perturbed by various extrinsic factors including the cytokine TNF, a cell signaling protein that mediates both proliferative and cytotoxic outcomes. Under conditions of infection and damage, defects in autophagy are associated with TNF-mediated cell death and tissue damage in the intestinal epithelium. However, a direct role of autophagy within the context of enterocyte cell death during homeostasis is lacking. Here, we generated mice lacking ATG14 (autophagy related 14) within the intestinal epithelium [ Atg14 f/f Vil1- Cre ( VC) + ]. These mice developed spontaneous villus loss and intestinal epithelial cell death within the small intestine. Based on marker studies, the increased cell death in these mice was due to apoptosis. Atg14 f/f VC + intestinal epithelial cells demonstrated sensitivity to TNF-triggered apoptosis. Correspondingly, both TNF blocking antibody and genetic deletion of Tnfrsf1a/Tnfr1 rescued villus loss and cell death phenotype in Atg14 f/f VC + mice. Lastly, we identified a similar pattern of spontaneous villus atrophy and cell death when Rb1cc1/ Fip200 was conditionally deleted from the intestinal epithelium ( Rb1cc1 f/f VC + ). Overall, these findings are consistent with the hypothesis that factors that control entry into the autophagy pathway are also required during homeostasis to prevent TNF triggered death in the intestine.

          Abbreviations: ANOVA: analysis of variance; Atg14: autophagy related 14; Atg16l1: autophagy related 16-like 1 (S. cerevisiae); Atg5: autophagy related 5; cCASP3: cleaved CASP3/caspase-3; cCASP8: cleaved CASP8/caspase-8; CHX: cycloheximide; EdU: 5-ethynyl-2´-deoxyuridine thymidine; f/f: flox/flox; H&E: hematoxylin and eosin; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; Nec-1: necrostatin-1; Rb1cc1/Fip200: RB1-inducible coiled-coil 1; Ripk1: receptor (TNFRSF)-interacting serine-threonine kinase 1; Ripk3: receptor (TNFRSF)-interacting serine-threonine kinase 3; Tnfrsf1a/Tnfr1: tumor necrosis factor receptor superfamily, member 1a; Tnf/ Tnfsf1a: tumor necrosis factor; VC: Vil1/villin 1-Cre

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          Author and article information

          Journal
          Autophagy
          Autophagy
          KAUP
          kaup20
          Autophagy
          Taylor & Francis
          1554-8627
          1554-8635
          2019
          3 April 2019
          : 15
          : 11
          : 1990-2001
          Affiliations
          Department of Pathology and Immunology, Washington University in St. Louis , St. Louis, MO, USA
          Author notes
          CONTACT Thaddeus S. Stappenbeck stappenb@ 123456wustl.edu Department of Pathology and Immunology, Washington University in St. Louis , St. Louis, MO 63110, USA
          [*]

          These authors contributed equally to this work.

          Author information
          http://orcid.org/0000-0002-4247-0647
          http://orcid.org/0000-0002-6023-3901
          Article
          PMC6844524 PMC6844524 6844524 1596495
          10.1080/15548627.2019.1596495
          6844524
          30894050
          ef2007c6-6c87-42ec-8741-427f1e3cd319
          © 2019 Informa UK Limited, trading as Taylor & Francis Group
          History
          : 15 September 2018
          : 21 February 2019
          : 26 February 2019
          Page count
          Figures: 6, References: 52, Pages: 12
          Funding
          Funded by: National Institutes of Health 10.13039/100000002
          Award ID: P30DK052574
          Funded by: Washington University Digestive Disease Research Core Center
          Award ID: T32 HL007317
          This work was supported by the Crohn’s & Colitis Foundation ; Kenneth Rainin Foundation; National Heart, Lung, and Blood Institute [T32 HL007317]; National Institutes of Health [P30DK052574].
          Categories
          Research Paper

          Apoptosis,autophagy,epithelial spheroids,villus loss,cell death

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