Evidence map›Paper›PMID 34302001›Full record

ArticleScientific reports2021

Estrogen-related receptor alpha (ERRα) is a key regulator of intestinal homeostasis and protects against colitis.

Allan Tran, Charlotte Scholtes, Mario Songane, Claudia Champagne, Luc Galarneau, Marie-Pier Levasseur, Nassima Fodil, Catherine Rosa Dufour, Vincent Giguère, Maya Saleh

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Transcriptional control of energy metabolism by nuclear receptors.Nature reviews. Molecular cell biology · 2022
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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 2 countries.

Allan TranDepartment of Microbiology and Immunology, McGill University, Montreal, QC, H3A 2B4, Canada.
Charlotte ScholtesGoodman Cancer Research Centre, McGill University, Montreal, QC, H3A 2B4, Canada.
Mario SonganeDepartment of Medicine, McGill University, Montreal, QC, H3G 0B1, Canada.
Claudia ChampagneDepartment of Medicine, McGill University, Montreal, QC, H3G 0B1, Canada.
Luc GalarneauCedars Cancer Centre, Medical Physics, McGill University Health Centre, Montreal, H4A 3J1, Canada.
Marie-Pier LevasseurGoodman Cancer Research Centre, McGill University, Montreal, QC, H3A 2B4, Canada.
Nassima FodilDepartment of Biochemistry, McGill University, Montreal, QC, H3A 2B4, Canada.
Catherine Rosa DufourGoodman Cancer Research Centre, McGill University, Montreal, QC, H3A 2B4, Canada.
Vincent GiguèreGoodman Cancer Research Centre, McGill University, Montreal, QC, H3A 2B4, Canada.
Maya SalehDepartment of Microbiology and Immunology, McGill University, Montreal, QC, H3A 2B4, Canada. msaleh@immuconcept.org.
McGill University Health Centre · CAMcGill University · CACentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The estrogen-related receptor alpha (ERRα) is a primary regulator of mitochondrial energy metabolism, function and dynamics, and has been implicated in autophagy and immune regulation. ERRα is abundantly expressed in the intestine and in cells of the immune system. However, its role in inflammatory bowel disease (IBD) remains unknown. Here, we report a protective role of ERRα in the intestine. We found that mice deficient in ERRα were susceptible to experimental colitis, exhibiting increased colon inflammation and tissue damage. This phenotype was mediated by impaired compensatory proliferation of intestinal epithelial cells (IEC) following injury, enhanced IEC apoptosis and necrosis and reduced mucus-producing goblet cell counts. Longitudinal analysis of the microbiota demonstrated that loss of ERRα lead to a reduction in microbiome α-diversity and depletion of healthy gut bacterial constituents. Mechanistically, ERRα mediated its protective effects by acting within the radio-resistant compartment of the intestine. It promoted disease tolerance through transcriptional control of key genes involved in intestinal tissue homeostasis and repair. These findings provide new insights on the role of ERRα in the gut and extends our current knowledge of nuclear receptors implicated in IBD.

Indexed as

AnimalsApoptosisCell ProliferationColitisColonDextran SulfateDisease Models, AnimalEnergy MetabolismERRalpha Estrogen-Related ReceptorHomeostasisHumansInflammationInflammatory Bowel DiseasesIntestinal MucosaMiceMicrobiotaDextran SulfateERRalpha Estrogen-Related ReceptorPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseReceptors, Estrogen

Identifiers

PMID34302001
PMCPMC8302669
OpenAlexW3186071417

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.