Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine

Summary: Homeostatic renewal and stress-related tissue regeneration rely on stem cell activity, which drives the replacement of damaged cells to maintain tissue integrity and function. The Jun N-terminal kinase (JNK) signaling pathway has been established as a critical regulator of tissue homeostasi...

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Main Authors: Juliane Mundorf, Colin D. Donohoe, Colin D. McClure, Tony D. Southall, Mirka Uhlirova
Format: Article
Language:English
Published: Elsevier 2019-06-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124719306369
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spelling doaj-4ed65337c57e4fa18d12e5c183f766cd2020-11-25T00:02:42ZengElsevierCell Reports2211-12472019-06-01271030193033.e5Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila IntestineJuliane Mundorf0Colin D. Donohoe1Colin D. McClure2Tony D. Southall3Mirka Uhlirova4Institute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne 50931, GermanyInstitute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne 50931, GermanyDepartment of Life Sciences, Imperial College London, Sir Ernst Chain Building, South Kensington Campus, London SW7 2AZ, UKDepartment of Life Sciences, Imperial College London, Sir Ernst Chain Building, South Kensington Campus, London SW7 2AZ, UKInstitute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne 50931, Germany; Center for Molecular Medicine Cologne, University of Cologne, Cologne 50931, Germany; Corresponding authorSummary: Homeostatic renewal and stress-related tissue regeneration rely on stem cell activity, which drives the replacement of damaged cells to maintain tissue integrity and function. The Jun N-terminal kinase (JNK) signaling pathway has been established as a critical regulator of tissue homeostasis both in intestinal stem cells (ISCs) and mature enterocytes (ECs), while its chronic activation has been linked to tissue degeneration and aging. Here, we show that JNK signaling requires the stress-inducible transcription factor Ets21c to promote tissue renewal in Drosophila. We demonstrate that Ets21c controls ISC proliferation as well as EC apoptosis through distinct sets of target genes that orchestrate cellular behaviors via intrinsic and non-autonomous signaling mechanisms. While its loss appears dispensable for development and prevents epithelial aging, ISCs and ECs demand Ets21c function to mount cellular responses to oxidative stress. Ets21c thus emerges as a vital regulator of proliferative homeostasis in the midgut and a determinant of the adult healthspan. : Mundorf et al. show that the conserved JNK signaling pathway requires the transcription factor Ets21c to mount cellular stress responses in the Drosophila adult intestine. Ets21c emerges as a critical regulator of tissue homeostasis that coordinates the apoptotic removal of differentiated enterocytes with compensatory stem cell proliferation. Keywords: Drosophila, stress signaling, regeneration, aging, intestine, stem cells, enterocytes, JNK, transcription factors, Ets21chttp://www.sciencedirect.com/science/article/pii/S2211124719306369
collection DOAJ
language English
format Article
sources DOAJ
author Juliane Mundorf
Colin D. Donohoe
Colin D. McClure
Tony D. Southall
Mirka Uhlirova
spellingShingle Juliane Mundorf
Colin D. Donohoe
Colin D. McClure
Tony D. Southall
Mirka Uhlirova
Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
Cell Reports
author_facet Juliane Mundorf
Colin D. Donohoe
Colin D. McClure
Tony D. Southall
Mirka Uhlirova
author_sort Juliane Mundorf
title Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
title_short Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
title_full Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
title_fullStr Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
title_full_unstemmed Ets21c Governs Tissue Renewal, Stress Tolerance, and Aging in the Drosophila Intestine
title_sort ets21c governs tissue renewal, stress tolerance, and aging in the drosophila intestine
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2019-06-01
description Summary: Homeostatic renewal and stress-related tissue regeneration rely on stem cell activity, which drives the replacement of damaged cells to maintain tissue integrity and function. The Jun N-terminal kinase (JNK) signaling pathway has been established as a critical regulator of tissue homeostasis both in intestinal stem cells (ISCs) and mature enterocytes (ECs), while its chronic activation has been linked to tissue degeneration and aging. Here, we show that JNK signaling requires the stress-inducible transcription factor Ets21c to promote tissue renewal in Drosophila. We demonstrate that Ets21c controls ISC proliferation as well as EC apoptosis through distinct sets of target genes that orchestrate cellular behaviors via intrinsic and non-autonomous signaling mechanisms. While its loss appears dispensable for development and prevents epithelial aging, ISCs and ECs demand Ets21c function to mount cellular responses to oxidative stress. Ets21c thus emerges as a vital regulator of proliferative homeostasis in the midgut and a determinant of the adult healthspan. : Mundorf et al. show that the conserved JNK signaling pathway requires the transcription factor Ets21c to mount cellular stress responses in the Drosophila adult intestine. Ets21c emerges as a critical regulator of tissue homeostasis that coordinates the apoptotic removal of differentiated enterocytes with compensatory stem cell proliferation. Keywords: Drosophila, stress signaling, regeneration, aging, intestine, stem cells, enterocytes, JNK, transcription factors, Ets21c
url http://www.sciencedirect.com/science/article/pii/S2211124719306369
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