author_facet Kajino-Sakamoto, Rie
Inagaki, Maiko
Lippert, Elisabeth
Akira, Shizuo
Robine, Sylvie
Matsumoto, Kunihiro
Jobin, Christian
Ninomiya-Tsuji, Jun
Kajino-Sakamoto, Rie
Inagaki, Maiko
Lippert, Elisabeth
Akira, Shizuo
Robine, Sylvie
Matsumoto, Kunihiro
Jobin, Christian
Ninomiya-Tsuji, Jun
author Kajino-Sakamoto, Rie
Inagaki, Maiko
Lippert, Elisabeth
Akira, Shizuo
Robine, Sylvie
Matsumoto, Kunihiro
Jobin, Christian
Ninomiya-Tsuji, Jun
spellingShingle Kajino-Sakamoto, Rie
Inagaki, Maiko
Lippert, Elisabeth
Akira, Shizuo
Robine, Sylvie
Matsumoto, Kunihiro
Jobin, Christian
Ninomiya-Tsuji, Jun
The Journal of Immunology
Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
Immunology
Immunology and Allergy
author_sort kajino-sakamoto, rie
spelling Kajino-Sakamoto, Rie Inagaki, Maiko Lippert, Elisabeth Akira, Shizuo Robine, Sylvie Matsumoto, Kunihiro Jobin, Christian Ninomiya-Tsuji, Jun 0022-1767 1550-6606 The American Association of Immunologists Immunology Immunology and Allergy http://dx.doi.org/10.4049/jimmunol.181.2.1143 <jats:title>Abstract</jats:title> <jats:p>Recent studies have revealed that TAK1 kinase is an essential intermediate in several innate immune signaling pathways. In this study, we investigated the role of TAK1 signaling in maintaining intestinal homeostasis by generating enterocyte-specific constitutive and inducible gene-deleted TAK1 mice. We found that enterocyte-specific constitutive TAK1-deleted mice spontaneously developed intestinal inflammation as observed by histological analysis and enhanced expression of IL-1β, MIP-2, and IL-6 around the time of birth, which was accompanied by significant enterocyte apoptosis. When TAK1 was deleted in the intestinal epithelium of 4-wk-old mice using an inducible knockout system, enterocytes underwent apoptosis and intestinal inflammation developed within 2–3 days following the initiation of gene deletion. We found that enterocyte apoptosis and intestinal inflammation were strongly attenuated when enterocyte-specific constitutive TAK1-deleted mice were crossed to TNF receptor 1−/− mice. However, these mice later (&amp;gt;14 days) developed ileitis and colitis. Thus, TAK1 signaling in enterocytes is essential for preventing TNF-dependent epithelium apoptosis and the TNF-independent development of ileitis and colitis. We propose that aberration in TAK1 signaling might disrupt intestinal homeostasis and favor the development of inflammatory disease.</jats:p> Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis The Journal of Immunology
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series The Journal of Immunology
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title Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_unstemmed Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_full Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_fullStr Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_full_unstemmed Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_short Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_sort enterocyte-derived tak1 signaling prevents epithelium apoptosis and the development of ileitis and colitis
topic Immunology
Immunology and Allergy
url http://dx.doi.org/10.4049/jimmunol.181.2.1143
publishDate 2008
physical 1143-1152
description <jats:title>Abstract</jats:title> <jats:p>Recent studies have revealed that TAK1 kinase is an essential intermediate in several innate immune signaling pathways. In this study, we investigated the role of TAK1 signaling in maintaining intestinal homeostasis by generating enterocyte-specific constitutive and inducible gene-deleted TAK1 mice. We found that enterocyte-specific constitutive TAK1-deleted mice spontaneously developed intestinal inflammation as observed by histological analysis and enhanced expression of IL-1β, MIP-2, and IL-6 around the time of birth, which was accompanied by significant enterocyte apoptosis. When TAK1 was deleted in the intestinal epithelium of 4-wk-old mice using an inducible knockout system, enterocytes underwent apoptosis and intestinal inflammation developed within 2–3 days following the initiation of gene deletion. We found that enterocyte apoptosis and intestinal inflammation were strongly attenuated when enterocyte-specific constitutive TAK1-deleted mice were crossed to TNF receptor 1−/− mice. However, these mice later (&amp;gt;14 days) developed ileitis and colitis. Thus, TAK1 signaling in enterocytes is essential for preventing TNF-dependent epithelium apoptosis and the TNF-independent development of ileitis and colitis. We propose that aberration in TAK1 signaling might disrupt intestinal homeostasis and favor the development of inflammatory disease.</jats:p>
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author Kajino-Sakamoto, Rie, Inagaki, Maiko, Lippert, Elisabeth, Akira, Shizuo, Robine, Sylvie, Matsumoto, Kunihiro, Jobin, Christian, Ninomiya-Tsuji, Jun
author_facet Kajino-Sakamoto, Rie, Inagaki, Maiko, Lippert, Elisabeth, Akira, Shizuo, Robine, Sylvie, Matsumoto, Kunihiro, Jobin, Christian, Ninomiya-Tsuji, Jun, Kajino-Sakamoto, Rie, Inagaki, Maiko, Lippert, Elisabeth, Akira, Shizuo, Robine, Sylvie, Matsumoto, Kunihiro, Jobin, Christian, Ninomiya-Tsuji, Jun
author_sort kajino-sakamoto, rie
container_issue 2
container_start_page 1143
container_title The Journal of Immunology
container_volume 181
description <jats:title>Abstract</jats:title> <jats:p>Recent studies have revealed that TAK1 kinase is an essential intermediate in several innate immune signaling pathways. In this study, we investigated the role of TAK1 signaling in maintaining intestinal homeostasis by generating enterocyte-specific constitutive and inducible gene-deleted TAK1 mice. We found that enterocyte-specific constitutive TAK1-deleted mice spontaneously developed intestinal inflammation as observed by histological analysis and enhanced expression of IL-1β, MIP-2, and IL-6 around the time of birth, which was accompanied by significant enterocyte apoptosis. When TAK1 was deleted in the intestinal epithelium of 4-wk-old mice using an inducible knockout system, enterocytes underwent apoptosis and intestinal inflammation developed within 2–3 days following the initiation of gene deletion. We found that enterocyte apoptosis and intestinal inflammation were strongly attenuated when enterocyte-specific constitutive TAK1-deleted mice were crossed to TNF receptor 1−/− mice. However, these mice later (&amp;gt;14 days) developed ileitis and colitis. Thus, TAK1 signaling in enterocytes is essential for preventing TNF-dependent epithelium apoptosis and the TNF-independent development of ileitis and colitis. We propose that aberration in TAK1 signaling might disrupt intestinal homeostasis and favor the development of inflammatory disease.</jats:p>
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spelling Kajino-Sakamoto, Rie Inagaki, Maiko Lippert, Elisabeth Akira, Shizuo Robine, Sylvie Matsumoto, Kunihiro Jobin, Christian Ninomiya-Tsuji, Jun 0022-1767 1550-6606 The American Association of Immunologists Immunology Immunology and Allergy http://dx.doi.org/10.4049/jimmunol.181.2.1143 <jats:title>Abstract</jats:title> <jats:p>Recent studies have revealed that TAK1 kinase is an essential intermediate in several innate immune signaling pathways. In this study, we investigated the role of TAK1 signaling in maintaining intestinal homeostasis by generating enterocyte-specific constitutive and inducible gene-deleted TAK1 mice. We found that enterocyte-specific constitutive TAK1-deleted mice spontaneously developed intestinal inflammation as observed by histological analysis and enhanced expression of IL-1β, MIP-2, and IL-6 around the time of birth, which was accompanied by significant enterocyte apoptosis. When TAK1 was deleted in the intestinal epithelium of 4-wk-old mice using an inducible knockout system, enterocytes underwent apoptosis and intestinal inflammation developed within 2–3 days following the initiation of gene deletion. We found that enterocyte apoptosis and intestinal inflammation were strongly attenuated when enterocyte-specific constitutive TAK1-deleted mice were crossed to TNF receptor 1−/− mice. However, these mice later (&amp;gt;14 days) developed ileitis and colitis. Thus, TAK1 signaling in enterocytes is essential for preventing TNF-dependent epithelium apoptosis and the TNF-independent development of ileitis and colitis. We propose that aberration in TAK1 signaling might disrupt intestinal homeostasis and favor the development of inflammatory disease.</jats:p> Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis The Journal of Immunology
spellingShingle Kajino-Sakamoto, Rie, Inagaki, Maiko, Lippert, Elisabeth, Akira, Shizuo, Robine, Sylvie, Matsumoto, Kunihiro, Jobin, Christian, Ninomiya-Tsuji, Jun, The Journal of Immunology, Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis, Immunology, Immunology and Allergy
title Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_full Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_fullStr Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_full_unstemmed Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_short Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
title_sort enterocyte-derived tak1 signaling prevents epithelium apoptosis and the development of ileitis and colitis
title_unstemmed Enterocyte-Derived TAK1 Signaling Prevents Epithelium Apoptosis and the Development of Ileitis and Colitis
topic Immunology, Immunology and Allergy
url http://dx.doi.org/10.4049/jimmunol.181.2.1143