Evidence map›Paper›PMID 32636391›Full record

ArticleNature communications2020

Enhancer and super-enhancer dynamics in repair after ischemic acute kidney injury.

Julia Wilflingseder, Michaela Willi, Hye Kyung Lee, Hannes Olauson, Jakub Jankowski, Takaharu Ichimura, Reinhold Erben, M Todd Valerius, Lothar Hennighausen, Joseph V Bonventre

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 102 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Julia Wilflingseder *Brigham and Women's Hospital, Renal Division, Harvard Medical School, 4 Blackfan Circle, Boston, MA, 02115, USA. julia.wilflingseder@vetmeduni.ac.at.ORCID http://orcid.org/0000-0002-0230-9349
Michaela Willi *Laboratory of Genetics and Physiology, NIDDK, NIH, 8 Center Dr, Bethesda, MD, 20814, USA.ORCID http://orcid.org/0000-0002-2248-1998
Hye Kyung LeeLaboratory of Genetics and Physiology, NIDDK, NIH, 8 Center Dr, Bethesda, MD, 20814, USA.ORCID http://orcid.org/0000-0002-7785-5942
Hannes OlausonBrigham and Women's Hospital, Renal Division, Harvard Medical School, 4 Blackfan Circle, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0001-9911-9201
Jakub JankowskiLaboratory of Genetics and Physiology, NIDDK, NIH, 8 Center Dr, Bethesda, MD, 20814, USA.
Takaharu IchimuraBrigham and Women's Hospital, Renal Division, Harvard Medical School, 4 Blackfan Circle, Boston, MA, 02115, USA.
Reinhold ErbenDepartment of Physiology and Pathophysiology, University of Veterinary Medicine, Veterinärplatz 1, 1210, Vienna, Austria.ORCID http://orcid.org/0000-0003-0801-6958
M Todd ValeriusBrigham and Women's Hospital, Renal Division, Harvard Medical School, 4 Blackfan Circle, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0001-8143-9231
Lothar HennighausenLaboratory of Genetics and Physiology, NIDDK, NIH, 8 Center Dr, Bethesda, MD, 20814, USA.
Joseph V BonventreBrigham and Women's Hospital, Renal Division, Harvard Medical School, 4 Blackfan Circle, Boston, MA, 02115, USA. joseph_bonventre@hms.harvard.edu.ORCID http://orcid.org/0000-0001-7144-386X
Brigham and Women's Hospital · USNational Institutes of Health · USUniversity of Veterinary Medicine Vienna · AT

Funding

Genetic Approaches To Understanding Organ Development and FunctionZIADK061000 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI HENNIGHAUSEN, LOTHAR · 2009 to 2025
$24.7M
KIDNEY INJURY MOLECULE-1 IN EPITHELIAL REPAIRR01DK072381 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 2005 to 2025
$8.6M
Mechanisms of Ischemic Kidney Injury and RepairR01DK039773 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI JOSEPH VINCENT BONVENTRE · 1987 to 2026
$6.2M
Mechanisms of Ischemic Kidney Injury and RepairR37DK039773 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 1993 to 2021
$5.2M
Kidney Microphysiological Analysis Platforms (MAP) to Optimize Function and Model DiseaseUH3TR002155 · NCATS · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT, LEE, LUKE P. · 2019 to 2021
$3.3M
Kidney Microphysiological Analysis Platforms (MAP) to Optimize Function and Model DiseaseUG3TR002155 · NCATS · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT, LEE, LUKE P. · 2017 to 2018
$2.0M
NCATS NIH HHS UG3 TR002155NCATS NIH HHS UH3 TR002155NIDDK NIH HHS R01 DK039773NIDDK NIH HHS R01 DK072381NIDDK NIH HHS R37 DK039773
6 · The paper itself

Abstract

The endogenous repair process can result in recovery after acute kidney injury (AKI) with adaptive proliferation of tubular epithelial cells, but repair can also lead to fibrosis and progressive kidney disease. There is currently limited knowledge about transcriptional regulators regulating these repair programs. Herein we establish the enhancer and super-enhancer landscape after AKI by ChIP-seq in uninjured and repairing kidneys on day two after ischemia reperfusion injury (IRI). We identify key transcription factors including HNF4A, GR, STAT3 and STAT5, which show specific binding at enhancer and super-enhancer sites, revealing enhancer dynamics and transcriptional changes during kidney repair. Loss of bromodomain-containing protein 4 function before IRI leads to impaired recovery after AKI and increased mortality. Our comprehensive analysis of epigenetic changes after kidney injury in vivo has the potential to identify targets for therapeutic intervention. Importantly, our data also call attention to potential caveats involved in use of BET inhibitors in patients at risk for AKI.

Indexed as

Enhancer Elements, GeneticAcute Kidney InjuryAmino Acid MotifsAnimalsBinding SitesBromodomain Containing ProteinsCell ProliferationEpigenesis, GeneticFibrosisHepatocyte Nuclear Factor 4KidneyKidney TubulesMaleMiceMice, Inbred BALB CMice, Inbred C57BLBrd4 protein, mouseBromodomain Containing ProteinsHepatocyte Nuclear Factor 4Hnf4a protein, mouseNuclear ProteinsReceptors, GlucocorticoidStat3 protein, mouseSTAT3 Transcription FactorSTAT5 Transcription FactorTranscription Factors

Identifiers

PMID32636391
PMCPMC7341735
OpenAlexW3040347016

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.