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      Ageing, metabolism and the intestine

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          Abstract

          The intestinal epithelium serves as a dynamic barrier to the environment and integrates a variety of signals, including those from metabolites, commensal microbiota, immune responses and stressors upon ageing. The intestine is constantly challenged and requires a high renewal rate to replace damaged cells in order to maintain its barrier function. Essential for its renewal capacity are intestinal stem cells, which constantly give rise to progenitor cells that differentiate into the multiple cell types present in the epithelium. Here, we review the current state of research of how metabolism and ageing control intestinal stem cell function and epithelial homeostasis. We focus on recent insights gained from model organisms that indicate how changes in metabolic signalling during ageing are a major driver for the loss of stem cell plasticity and epithelial homeostasis, ultimately affecting the resilience of an organism and limiting its lifespan. We compare findings made in mouse and Drosophila and discuss differences and commonalities in the underlying signalling pathways and mechanisms in the context of ageing.

          Abstract

          The intestinal epithelium plays important roles in nutrition, signaling and as a barrier to the environment. Intestinal stem cells are crucial to replace epithelial cells and to maintain epithelial homeostasis. This review discusses how aging and metabolism affect stem cell function and epithelial homeostasis in the mouse and fly intestine.

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          Most cited references165

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          Cytokine/Jak/Stat signaling mediates regeneration and homeostasis in the Drosophila midgut.

          Cells in intestinal epithelia turn over rapidly due to damage from digestion and toxins produced by the enteric microbiota. Gut homeostasis is maintained by intestinal stem cells (ISCs) that divide to replenish the intestinal epithelium, but little is known about how ISC division and differentiation are coordinated with epithelial cell loss. We show here that when enterocytes (ECs) in the Drosophila midgut are subjected to apoptosis, enteric infection, or JNK-mediated stress signaling, they produce cytokines (Upd, Upd2, and Upd3) that activate Jak/Stat signaling in ISCs, promoting their rapid division. Upd/Jak/Stat activity also promotes progenitor cell differentiation, in part by stimulating Delta/Notch signaling, and is required for differentiation in both normal and regenerating midguts. Hence, cytokine-mediated feedback enables stem cells to replace spent progeny as they are lost, thereby establishing gut homeostasis.
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            Evidence that stem cells reside in the adult Drosophila midgut epithelium.

            Adult stem cells maintain organ systems throughout the course of life and facilitate repair after injury or disease. A fundamental property of stem and progenitor cell division is the capacity to retain a proliferative state or generate differentiated daughter cells; however, little is currently known about signals that regulate the balance between these processes. Here, we characterize a proliferating cellular compartment in the adult Drosophila midgut. Using genetic mosaic analysis we demonstrate that differentiated cells in the epithelium arise from a common lineage. Furthermore, we show that reduction of Notch signalling leads to an increase in the number of midgut progenitor cells, whereas activation of the Notch pathway leads to a decrease in proliferation. Thus, the midgut progenitor's default state is proliferation, which is inhibited through the Notch signalling pathway. The ability to identify, manipulate and genetically trace cell lineages in the midgut should lead to the discovery of additional genes that regulate stem and progenitor cell biology in the gastrointestinal tract.
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              Tales from the crypt: new insights into intestinal stem cells

              The intestinal epithelium withstands continuous mechanical, chemical and biological insults despite its single-layered, simple epithelial structure. The crypt-villus tissue architecture in combination with rapid cell turnover enables the intestine to act both as a barrier and as the primary site of nutrient uptake. Constant tissue replenishment is fuelled by continuously dividing stem cells that reside at the bottom of crypts. These cells are nurtured and protected by specialized epithelial and mesenchymal cells, and together constitute the intestinal stem cell niche. Intestinal stem cells and early progenitor cells compete for limited niche space and, therefore, the ability to retain or regain stemness. Those cells unable to do so differentiate to one of six different mature cell types and move upwards towards the villus, where they are shed into the intestinal lumen after 3-5 days. In this Review, we discuss the signals, cell types and mechanisms that control homeostasis and regeneration in the intestinal epithelium. We investigate how the niche protects and instructs intestinal stem cells, which processes drive differentiation of mature cells and how imbalance in key signalling pathways can cause human disease.
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                Author and article information

                Contributors
                m.boutros@dkfz.de
                Journal
                EMBO Rep
                EMBO Rep
                10.1002/(ISSN)1469-3178
                EMBR
                embor
                EMBO Reports
                John Wiley and Sons Inc. (Hoboken )
                1469-221X
                1469-3178
                21 June 2020
                03 July 2020
                21 June 2020
                : 21
                : 7 ( doiID: 10.1002/embr.v21.7 )
                : e50047
                Affiliations
                [ 1 ] Division Signaling and Functional Genomics German Cancer Research Center (DKFZ) Heidelberg University Heidelberg Germany
                Author notes
                [*] [* ]Corresponding author. Tel: +49(0) 6221 42 1951; E‐mail: m.boutros@ 123456dkfz.de
                [†]

                These authors contributed equally to this work

                Author information
                https://orcid.org/0000-0002-6007-1164
                https://orcid.org/0000-0002-2101-9304
                https://orcid.org/0000-0002-9458-817X
                Article
                EMBR202050047
                10.15252/embr.202050047
                7332987
                32567155
                76946e68-4973-4ffc-aedf-a1036a1db3df
                © 2020 The Authors. Published under the terms of the CC BY 4.0 license

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 16 January 2020
                : 18 April 2020
                : 29 May 2020
                Page count
                Figures: 5, Tables: 2, Pages: 22, Words: 19065
                Funding
                Funded by: DFG , open-funder-registry 10.13039/100004807;
                Award ID: SFB873
                Funded by: ERC SYNERGY
                Funded by: AMPro
                Categories
                Review
                Review
                Custom metadata
                2.0
                03 July 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.5 mode:remove_FC converted:03.07.2020

                Molecular biology
                ageing,epithelial barriers,intestinal homeostasis,metabolism,stem cells,molecular biology of disease,regenerative medicine

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