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Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis

Authors :
Koningin Wilhelmina Fonds
Fondation Charcot
Foundation Against Cancer
Ghent University
Universidad de Salamanca
Ministerio de Economía y Competitividad (España)
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
Crohn's and Colitis Foundation of America
Junta de Castilla y León
Instituto de Salud Carlos III
Slowicka, Karolina
Serramito-Gómez, Inmaculada
Boada-Romero, Emilio
Martens, Arne
Sze, Mozes
Petta, Ioanna
Vikkula, Hanna K.
Rycke, Riet De
Parthoens, Eef
Lippens, Saskia
Savvides, S.
Wullaert, Andy
Vereecke, Lars
Pimentel-Muiños, Felipe X.
Loo, Geert van
Koningin Wilhelmina Fonds
Fondation Charcot
Foundation Against Cancer
Ghent University
Universidad de Salamanca
Ministerio de Economía y Competitividad (España)
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
Crohn's and Colitis Foundation of America
Junta de Castilla y León
Instituto de Salud Carlos III
Slowicka, Karolina
Serramito-Gómez, Inmaculada
Boada-Romero, Emilio
Martens, Arne
Sze, Mozes
Petta, Ioanna
Vikkula, Hanna K.
Rycke, Riet De
Parthoens, Eef
Lippens, Saskia
Savvides, S.
Wullaert, Andy
Vereecke, Lars
Pimentel-Muiños, Felipe X.
Loo, Geert van
Publication Year :
2019

Abstract

Prevention of inflammatory bowel disease (IBD) relies on tight control of inflammatory, cell death and autophagic mechanisms, but how these pathways are integrated at the molecular level is still unclear. Here we show that the anti-inflammatory protein A20 and the critical autophagic mediator Atg16l1 physically interact and synergize to regulate the stability of the intestinal epithelial barrier. A proteomic screen using the WD40 domain of ATG16L1 (WDD) identified A20 as a WDD-interacting protein. Loss of A20 and Atg16l1 in mouse intestinal epithelium induces spontaneous IBD-like pathology, as characterized by severe inflammation and increased intestinal epithelial cell death in both small and large intestine. Mechanistically, absence of A20 promotes Atg16l1 accumulation, while elimination of Atg16l1 or expression of WDD-deficient Atg16l1 stabilizes A20. Collectively our data show that A20 and Atg16l1 cooperatively control intestinal homeostasis by acting at the intersection of inflammatory, autophagy and cell death pathways.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286539842
Document Type :
Electronic Resource