Evidence map›Paper›PMID 33809055›Full record

ArticleInternational journal of molecular sciences2021

Adipocyte-Mineralocorticoid Receptor Alters Mitochondrial Quality Control Leading to Mitochondrial Dysfunction and Senescence of Visceral Adipose Tissue.

Clara Lefranc, Malou Friederich-Persson, Fabienne Foufelle, Aurélie Nguyen Dinh Cat, Frédéric Jaisser

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  9. The mineralocorticoid receptor in diabetic kidney disease.American journal of physiology. Renal physiology · 2024
    Review
  10. Review
  11. Mitochondria in Ageing and Diseases: Partie Deux.International journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
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  16. Targeting mineralocorticoid receptors in diet-induced hepatic steatosis and insulin resistance.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  17. Review
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

5 authors at 2 institutions in 2 countries.

Clara LefrancCentre de Recherche des Cordeliers, Inserm, Sorbonne Université, Université de Paris, Team Metabolic Diseases, Diabetes and Comorbidities, 75006 Paris, France.ORCID 0000-0003-4635-136X
Malou Friederich-PerssonDepartment of Medical Cell Biology, Uppsala University, 751 23 Uppsala, Sweden.
Fabienne FoufelleCentre de Recherche des Cordeliers, Inserm, Sorbonne Université, Université de Paris, Team Metabolic Diseases, Diabetes and Comorbidities, 75006 Paris, France.
Aurélie Nguyen Dinh CatCentre de Recherche des Cordeliers, Inserm, Sorbonne Université, Université de Paris, Team Metabolic Diseases, Diabetes and Comorbidities, 75006 Paris, France.ORCID 0000-0002-3007-5332
Frédéric JaisserCentre de Recherche des Cordeliers, Inserm, Sorbonne Université, Université de Paris, Team Metabolic Diseases, Diabetes and Comorbidities, 75006 Paris, France.
Inserm · FRUppsala University · SE

Funding

Agence Nationale de la Recherche ANR-15- RHUS-0003Åke Wiberg StiftelseFondation de France CARDIO 00086498Institut National de la Santé et de la Recherche Médicale operating budgetInstitut National de la Santé et de la Recherche Médicale poste d'accueilMagnus Bergvalls StiftelseWenner-Gren Foundation
6 · The paper itself

Abstract

Mineralocorticoid receptor (MR) expression is increased in the adipose tissue (AT) of obese patients and animals. We previously demonstrated that adipocyte-MR overexpression in mice (Adipo-MROE mice) is associated with metabolic alterations. Moreover, we showed that MR regulates mitochondrial dysfunction and cellular senescence in the visceral AT of obese db/db mice. Our hypothesis is that adipocyte-MR overactivation triggers mitochondrial dysfunction and cellular senescence, through increased mitochondrial oxidative stress (OS). Using the Adipo-MROE mice with conditional adipocyte-MR expression, we evaluated the specific effects of adipocyte-MR on global and mitochondrial OS, as well as on OS-induced damage. Mitochondrial function was assessed by high throughput respirometry. Molecular mechanisms were probed in AT focusing on mitochondrial quality control and senescence markers. Adipo-MROE mice exhibited increased mitochondrial OS and altered mitochondrial respiration, associated with reduced biogenesis and increased fission. This was associated with OS-induced DNA-damage and AT premature senescence. In conclusion, targeted adipocyte-MR overexpression leads to an imbalance in mitochondrial dynamics and regeneration, to mitochondrial dysfunction and to ageing in visceral AT. These data bring new insights into the MR-dependent AT dysfunction in obesity.

Indexed as

3T3-L1 CellsAdipocytesAnimalsCellular SenescenceHumansIntra-Abdominal FatMiceMitochondriaMitochondrial DynamicsObesityOxidative StressReceptors, MineralocorticoidReceptors, Mineralocorticoidadipose tissuemetabolic syndromemineralocorticoid receptormitochondrial dysfunctionoxidative stresssenescence

Identifiers

PMID33809055
PMCPMC8001019
OpenAlexW3138685792

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.