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Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis
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 Atg16l...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478926/ https://www.ncbi.nlm.nih.gov/pubmed/31015422 http://dx.doi.org/10.1038/s41467-019-09667-z |
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author | Slowicka, Karolina Serramito-Gómez, Inmaculada Boada-Romero, Emilio Martens, Arne Sze, Mozes Petta, Ioanna Vikkula, Hanna K. De Rycke, Riet Parthoens, Eef Lippens, Saskia Savvides, Savvas N. Wullaert, Andy Vereecke, Lars Pimentel-Muiños, Felipe X. van Loo, Geert |
author_facet | Slowicka, Karolina Serramito-Gómez, Inmaculada Boada-Romero, Emilio Martens, Arne Sze, Mozes Petta, Ioanna Vikkula, Hanna K. De Rycke, Riet Parthoens, Eef Lippens, Saskia Savvides, Savvas N. Wullaert, Andy Vereecke, Lars Pimentel-Muiños, Felipe X. van Loo, Geert |
author_sort | Slowicka, Karolina |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6478926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64789262019-04-25 Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis Slowicka, Karolina Serramito-Gómez, Inmaculada Boada-Romero, Emilio Martens, Arne Sze, Mozes Petta, Ioanna Vikkula, Hanna K. De Rycke, Riet Parthoens, Eef Lippens, Saskia Savvides, Savvas N. Wullaert, Andy Vereecke, Lars Pimentel-Muiños, Felipe X. van Loo, Geert Nat Commun Article 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. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478926/ /pubmed/31015422 http://dx.doi.org/10.1038/s41467-019-09667-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Slowicka, Karolina Serramito-Gómez, Inmaculada Boada-Romero, Emilio Martens, Arne Sze, Mozes Petta, Ioanna Vikkula, Hanna K. De Rycke, Riet Parthoens, Eef Lippens, Saskia Savvides, Savvas N. Wullaert, Andy Vereecke, Lars Pimentel-Muiños, Felipe X. van Loo, Geert Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title | Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title_full | Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title_fullStr | Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title_full_unstemmed | Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title_short | Physical and functional interaction between A20 and ATG16L1-WD40 domain in the control of intestinal homeostasis |
title_sort | physical and functional interaction between a20 and atg16l1-wd40 domain in the control of intestinal homeostasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478926/ https://www.ncbi.nlm.nih.gov/pubmed/31015422 http://dx.doi.org/10.1038/s41467-019-09667-z |
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