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Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death

Lgr5(+) intestinal stem cells are crucial for fast homeostatic renewal of intestinal epithelium and Wnt/β-catenin signaling plays an essential role in this process by sustaining stem cell self-renewal. The poly(ADP-ribose) polymerases tankyrases (TNKSs) mediate protein poly-ADP-ribosylation and are...

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Autores principales: Ye, Pan, Chiang, Y. Jeffrey, Qi, Zhen, Li, Yehua, Wang, Shan, Liu, Yuan, Li, Xintong, Chen, Ye-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177203/
https://www.ncbi.nlm.nih.gov/pubmed/30260955
http://dx.doi.org/10.1371/journal.pgen.1007697
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author Ye, Pan
Chiang, Y. Jeffrey
Qi, Zhen
Li, Yehua
Wang, Shan
Liu, Yuan
Li, Xintong
Chen, Ye-Guang
author_facet Ye, Pan
Chiang, Y. Jeffrey
Qi, Zhen
Li, Yehua
Wang, Shan
Liu, Yuan
Li, Xintong
Chen, Ye-Guang
author_sort Ye, Pan
collection PubMed
description Lgr5(+) intestinal stem cells are crucial for fast homeostatic renewal of intestinal epithelium and Wnt/β-catenin signaling plays an essential role in this process by sustaining stem cell self-renewal. The poly(ADP-ribose) polymerases tankyrases (TNKSs) mediate protein poly-ADP-ribosylation and are involved in multiple cellular processes such as Wnt signaling regulation, mitotic progression and telomere maintenance. However, little is known about the physiological function of TNKSs in epithelium homeostasis regulation. Here, using Villin-creERT2;Tnks1(-/-);Tnks2(fl/fl) (DKO) mice, we observed that loss of TNKSs causes a rapid decrease of Lgr5(+) intestinal stem cells and magnified apoptosis in small intestinal crypts, leading to intestine degeneration and increased mouse mortality. Consistently, deletion of Tnks or blockage of TNKS activity with the inhibitor XAV939 significantly inhibits the growth of intestinal organoids. We further showed that the Wnt signaling agonist CHIR99021 sustains the growth of DKO organoids, and XAV939 does not cause growth retardation of Apc(-/-) organoids. Consistent with the promoting function of TNKSs in Wnt signaling, Wnt/β-catenin signaling is significantly decreased with stabilized Axin in DKO crypts. Together, our findings unravel the essential role of TNKSs-mediated protein parsylation in small intestinal homeostasis by modulating Wnt/β-catenin signaling.
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spelling pubmed-61772032018-10-19 Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death Ye, Pan Chiang, Y. Jeffrey Qi, Zhen Li, Yehua Wang, Shan Liu, Yuan Li, Xintong Chen, Ye-Guang PLoS Genet Research Article Lgr5(+) intestinal stem cells are crucial for fast homeostatic renewal of intestinal epithelium and Wnt/β-catenin signaling plays an essential role in this process by sustaining stem cell self-renewal. The poly(ADP-ribose) polymerases tankyrases (TNKSs) mediate protein poly-ADP-ribosylation and are involved in multiple cellular processes such as Wnt signaling regulation, mitotic progression and telomere maintenance. However, little is known about the physiological function of TNKSs in epithelium homeostasis regulation. Here, using Villin-creERT2;Tnks1(-/-);Tnks2(fl/fl) (DKO) mice, we observed that loss of TNKSs causes a rapid decrease of Lgr5(+) intestinal stem cells and magnified apoptosis in small intestinal crypts, leading to intestine degeneration and increased mouse mortality. Consistently, deletion of Tnks or blockage of TNKS activity with the inhibitor XAV939 significantly inhibits the growth of intestinal organoids. We further showed that the Wnt signaling agonist CHIR99021 sustains the growth of DKO organoids, and XAV939 does not cause growth retardation of Apc(-/-) organoids. Consistent with the promoting function of TNKSs in Wnt signaling, Wnt/β-catenin signaling is significantly decreased with stabilized Axin in DKO crypts. Together, our findings unravel the essential role of TNKSs-mediated protein parsylation in small intestinal homeostasis by modulating Wnt/β-catenin signaling. Public Library of Science 2018-09-27 /pmc/articles/PMC6177203/ /pubmed/30260955 http://dx.doi.org/10.1371/journal.pgen.1007697 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Ye, Pan
Chiang, Y. Jeffrey
Qi, Zhen
Li, Yehua
Wang, Shan
Liu, Yuan
Li, Xintong
Chen, Ye-Guang
Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title_full Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title_fullStr Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title_full_unstemmed Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title_short Tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
title_sort tankyrases maintain homeostasis of intestinal epithelium by preventing cell death
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177203/
https://www.ncbi.nlm.nih.gov/pubmed/30260955
http://dx.doi.org/10.1371/journal.pgen.1007697
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