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Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo

Understanding the transcription factors that modulate epithelial resistance to injury is necessary for understanding intestinal homeostasis and injury repair processes. Recently, transcription factor EB (TFEB) was implicated in expression of autophagy and host defense genes in nematodes and mammalia...

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Autores principales: Murano, Tatsuro, Najibi, Mehran, Paulus, Geraldine L. C., Adiliaghdam, Fatemeh, Valencia-Guerrero, Aida, Selig, Martin, Wang, Xiaofei, Jeffrey, Kate, Xavier, Ramnik J., Lassen, Kara G., Irazoqui, Javier E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655326/
https://www.ncbi.nlm.nih.gov/pubmed/29066772
http://dx.doi.org/10.1038/s41598-017-14370-4
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author Murano, Tatsuro
Najibi, Mehran
Paulus, Geraldine L. C.
Adiliaghdam, Fatemeh
Valencia-Guerrero, Aida
Selig, Martin
Wang, Xiaofei
Jeffrey, Kate
Xavier, Ramnik J.
Lassen, Kara G.
Irazoqui, Javier E.
author_facet Murano, Tatsuro
Najibi, Mehran
Paulus, Geraldine L. C.
Adiliaghdam, Fatemeh
Valencia-Guerrero, Aida
Selig, Martin
Wang, Xiaofei
Jeffrey, Kate
Xavier, Ramnik J.
Lassen, Kara G.
Irazoqui, Javier E.
author_sort Murano, Tatsuro
collection PubMed
description Understanding the transcription factors that modulate epithelial resistance to injury is necessary for understanding intestinal homeostasis and injury repair processes. Recently, transcription factor EB (TFEB) was implicated in expression of autophagy and host defense genes in nematodes and mammalian cells. However, the in vivo roles of TFEB in the mammalian intestinal epithelium were not known. Here, we used mice with a conditional deletion of Tfeb in the intestinal epithelium (Tfeb (ΔIEC)) to examine its importance in defense against injury. Unperturbed Tfeb (ΔIEC) mice exhibited grossly normal intestinal epithelia, except for a defect in Paneth cell granules. Tfeb (ΔIEC) mice exhibited lower levels of lipoprotein ApoA1 expression, which is downregulated in Crohn’s disease patients and causally linked to colitis susceptibility. Upon environmental epithelial injury using dextran sodium sulfate (DSS), Tfeb (ΔIEC) mice exhibited exaggerated colitis. Thus, our study reveals that TFEB is critical for resistance to intestinal epithelial cell injury, potentially mediated by APOA1.
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spelling pubmed-56553262017-10-31 Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo Murano, Tatsuro Najibi, Mehran Paulus, Geraldine L. C. Adiliaghdam, Fatemeh Valencia-Guerrero, Aida Selig, Martin Wang, Xiaofei Jeffrey, Kate Xavier, Ramnik J. Lassen, Kara G. Irazoqui, Javier E. Sci Rep Article Understanding the transcription factors that modulate epithelial resistance to injury is necessary for understanding intestinal homeostasis and injury repair processes. Recently, transcription factor EB (TFEB) was implicated in expression of autophagy and host defense genes in nematodes and mammalian cells. However, the in vivo roles of TFEB in the mammalian intestinal epithelium were not known. Here, we used mice with a conditional deletion of Tfeb in the intestinal epithelium (Tfeb (ΔIEC)) to examine its importance in defense against injury. Unperturbed Tfeb (ΔIEC) mice exhibited grossly normal intestinal epithelia, except for a defect in Paneth cell granules. Tfeb (ΔIEC) mice exhibited lower levels of lipoprotein ApoA1 expression, which is downregulated in Crohn’s disease patients and causally linked to colitis susceptibility. Upon environmental epithelial injury using dextran sodium sulfate (DSS), Tfeb (ΔIEC) mice exhibited exaggerated colitis. Thus, our study reveals that TFEB is critical for resistance to intestinal epithelial cell injury, potentially mediated by APOA1. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5655326/ /pubmed/29066772 http://dx.doi.org/10.1038/s41598-017-14370-4 Text en © The Author(s) 2017 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
Murano, Tatsuro
Najibi, Mehran
Paulus, Geraldine L. C.
Adiliaghdam, Fatemeh
Valencia-Guerrero, Aida
Selig, Martin
Wang, Xiaofei
Jeffrey, Kate
Xavier, Ramnik J.
Lassen, Kara G.
Irazoqui, Javier E.
Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title_full Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title_fullStr Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title_full_unstemmed Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title_short Transcription factor TFEB cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
title_sort transcription factor tfeb cell-autonomously modulates susceptibility to intestinal epithelial cell injury in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655326/
https://www.ncbi.nlm.nih.gov/pubmed/29066772
http://dx.doi.org/10.1038/s41598-017-14370-4
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