Evidence map›Paper›PMID 31958521›Full record

ArticleCellular and molecular gastroenterology and hepatology2020

ATF2 and ATF7 Are Critical Mediators of Intestinal Epithelial Repair.

Bartolomeus J Meijer, Francesca P Giugliano, Bart Baan, Jonathan H M van der Meer, Sander Meisner, Manon van Roest, Pim J Koelink, Ruben J de Boer, Nic Jones, Wolfgang Breitwieser and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. ATF7-PINK1 Axis Governs Mitophagy and Intestinal Inflammation in Ulcerative Colitis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  7. Article
  8. Article
  9. Article
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  12. Review
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  14. Review
  15. Article
  16. Intestine, Heal Thyself! Regulating the Intestinal Epithelial Response to Injury.Cellular and molecular gastroenterology and hepatology · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 3 countries.

Bartolomeus J MeijerDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands. Electronic address: b.j.meijer@amsterdamumc.nl.
Francesca P GiuglianoDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Bart BaanDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Jonathan H M van der MeerDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Sander MeisnerDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Manon van RoestDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Pim J KoelinkDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Ruben J de BoerDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Nic JonesDepartment of Cell Regulation, Cancer Research United Kingdom Manchester Institute, University of Manchester, Manchester, United Kingdom.
Wolfgang BreitwieserDepartment of Cell Regulation, Cancer Research United Kingdom Manchester Institute, University of Manchester, Manchester, United Kingdom.
Nicole N van der WelDepartment of Medical Biology, Electron Microscopy Center Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
Manon E WildenbergDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
Gijs R van den BrinkDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands; Roche Innovation Center Basel, F. Hoffmann-La Roche Associate Group, Basel, Switzerland.
Jarom HeijmansDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands; Department of Internal Medicine, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Vanesa MuncanDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology & Metabolism, Tytgat Institute for Liver and Intestinal Research, University of Amsterdam, Amsterdam, The Netherlands.
University of Amsterdam · NLUniversity of Manchester · GBAmsterdam University Medical Centers · NLRoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsActivation factor-1 transcription factor family members activating transcription factors 2 and 7 (ATF2 and ATF7) have highly redundant functions owing to highly homologous DNA binding sites. Their role in intestinal epithelial homeostasis and repair is unknown. Here, we assessed the role of these proteins in these conditions in an intestine-specific mouse model.

methodsWe performed in vivo and ex vivo experiments using Villin-Cre

resultsActivating phosphorylation of ATF2 and ATF7 was detected mainly in the crypts of the small intestine and the lower crypt region of the colonic epithelium. Under homeostatic conditions, no major phenotypic changes were detectable in the intestine of ATF mutant mice. However, on DSS exposure or whole-body irradiation, the intestinal epithelium showed a clearly impaired regenerative response. Mutant mice developed severe ulceration and inflammation associated with increased epithelial apoptosis on DSS exposure and were less able to regenerate colonic crypts on irradiation. In vitro, organoids derived from double-mutant epithelium had a growth disadvantage compared with wild-type organoids, impaired wound healing capacity in scratch assay, and increased sensitivity to tumor necrosis factor-α-induced damage.

conclusionsATF2 and ATF7 are dispensable for epithelial homeostasis, but are required to maintain epithelial regenerative capacity and protect against cell death during intestinal epithelial damage and repair.

Indexed as

RegenerationActivating Transcription Factor 2Activating Transcription FactorsAnimalsApoptosisCell DifferentiationCell ProliferationCells, CulturedColitis, UlcerativeColonDextran SulfateDisease Models, AnimalEpithelial CellsHumansIntestinal MucosaMiceActivating Transcription Factor 2Activating Transcription FactorsAtf2 protein, mouseATF7 protein, mouseDextran SulfateAP-1DSSProliferationTNF-α

Identifiers

PMID31958521
PMCPMC7210476
OpenAlexW2998998607

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.