Evidence map›Paper›PMID 26077864›Full record

ArticleNature communications2015

DJ-1 links muscle ROS production with metabolic reprogramming and systemic energy homeostasis in mice.

Sally Yu Shi, Shun-Yan Lu, Tharini Sivasubramaniyam, Xavier S Revelo, Erica P Cai, Cynthia T Luk, Stephanie A Schroer, Prital Patel, Raymond H Kim, Eric Bombardier and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. 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
6.0field-weighted citation impact, top 3% 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, 83 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Accelerated Sarcopenia Phenotype in the DJ-1/Antioxidants (Basel, Switzerland) · 2024
    Article
  9. Article
  10. Isolation and Identification ofMicroorganisms · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. PARK7/DJ-1 as a Therapeutic Target in Gut-Brain Axis Diseases.International journal of molecular sciences · 2022
    Review
  16. Article
  17. Review
  18. Parkinson's disease protein PARK7 prevents metabolite and protein damage caused by a glycolytic metabolite.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Review
  20. Article
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

15 authors at 5 institutions in 1 country.

Sally Yu Shi1] Toronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Ontario M5G 2M9, Canada.
Shun-Yan LuToronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada.
Tharini Sivasubramaniyam1] Toronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Ontario M5G 2M9, Canada.
Xavier S ReveloToronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada.
Erica P Cai1] Toronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Ontario M5G 2M9, Canada.
Cynthia T Luk1] Toronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Ontario M5G 2M9, Canada.
Stephanie A SchroerToronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada.
Prital PatelToronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada.
Raymond H KimThe Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2C1, Canada.
Eric BombardierDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Joe QuadrilateroDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
A Russell TuplingDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Tak W MakThe Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2C1, Canada.
Daniel A WinerToronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada.
Minna Woo1] Toronto General Research Institute, University Health Network, MaRS Centre, TMDT, 101 College Street, 10th floor, Room 10-363, Toronto, Ontario M5G 1L7, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Ontario M5G 2M9, Canada [3] Division of Endocrinology and Metabolism, Department of Medicine, University Health Network, University of Toronto, Toronto, Ontario M5G 2C4, Canada.
University Health Network · CAUniversity of Toronto · CAUniversity of Waterloo · CAOntario Institute for Cancer Research · CALunenfeld-Tanenbaum Research Institute · CA

Funding

Canadian Institutes of Health Research MOP-81148Canadian Institutes of Health Research MOP-93707
6 · The paper itself

Abstract

Reactive oxygen species (ROS) have been linked to a wide variety of pathologies, including obesity and diabetes, but ROS also act as endogenous signalling molecules, regulating numerous biological processes. DJ-1 is one of the most evolutionarily conserved proteins across species, and mutations in DJ-1 have been linked to some cases of Parkinson's disease. Here we show that DJ-1 maintains cellular metabolic homeostasis via modulating ROS levels in murine skeletal muscles, revealing a role of DJ-1 in maintaining efficient fuel utilization. We demonstrate that, in the absence of DJ-1, ROS uncouple mitochondrial respiration and activate AMP-activated protein kinase, which triggers Warburg-like metabolic reprogramming in muscle cells. Accordingly, DJ-1 knockout mice exhibit higher energy expenditure and are protected from obesity, insulin resistance and diabetes in the setting of fuel surplus. Our data suggest that promoting mitochondrial uncoupling may be a potential strategy for the treatment of obesity-associated metabolic disorders.

Indexed as

Adipose TissueAMP-Activated Protein KinasesAnimalsCell LineCell SurvivalDiabetes MellitusDiet, High-FatEnergy MetabolismGlucoseGlycolysisHomeostasisImmunoblottingInsulin ResistanceMiceMice, KnockoutMitochondriaAMP-Activated Protein KinasesGlucoseOncogene ProteinsPARK7 protein, mousePeroxiredoxinsProtein Deglycase DJ-1Reactive Oxygen Species

Identifiers

PMID26077864
PMCPMC4490365
OpenAlexW2271650132

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.