Evidence map›Paper›PMID 21326874›Full record

ArticlePloS one2011

Autoantibodies to endothelial cell surface ATP synthase, the endogenous receptor for hsp60, might play a pathogenic role in vasculatides.

Jean-Eric Alard, Sophie Hillion, Loïc Guillevin, Alain Saraux, Jacques-Olivier Pers, Pierre Youinou, Christophe Jamin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. 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
1.5field-weighted citation impact, top 19% 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, 42 citations in OpenAlex.

  1. Review
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  5. The role of mitochondria in rheumatic diseases.Nature reviews. Rheumatology · 2022
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  13. Proteomic profiling of aging in glomeruli of mice by using two-dimensional differential gel electrophoresis.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Article
  14. Article
  15. Review
  16. Mitochondria: master regulators of danger signalling.Nature reviews. Molecular cell biology · 2012
    Review
  17. 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

7 authors at 5 institutions in 1 country.

Jean-Eric AlardEA2216 "Immunology and Pathology" and IFR 148 ScInBioS, Université de Brest and Université Européenne de Bretagne, Brest, France.
Sophie Hillion
Loïc Guillevin
Alain Saraux
Jacques-Olivier Pers
Pierre Youinou
Christophe Jamin
Centre Hospitalier Régional Universitaire de Brest · FRUniversité de Bretagne Occidentale · FRBipar · FRHôpital Cochin · FRUniversité Européenne de Bretagne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeat shock protein (hsp) 60 that provides "danger signal" binds to the surface of resting endothelial cells (EC) but its receptor has not yet been characterized. In mitochondria, hsp60 specifically associates with adenosine triphosphate (ATP) synthase. We therefore examined the possible interaction between hsp60 and ATP synthase on EC surface. METHODOLOGY/PRINCIPAL

findingsUsing Far Western blot approach, co-immunoprecipitation studies and surface plasmon resonance analyses, we demonstrated that hsp60 binds to the β-subunit of ATP synthase. As a cell surface-expressed molecule, ATP synthase is potentially targeted by anti-EC-antibodies (AECAs) found in the sera of patients suffering vasculitides. Based on enzyme-linked immunosorbent assay and Western blotting techniques with F1-ATP synthase as substrate, we established the presence of anti-ATP synthase antibodies at higher frequency in patients with primary vasculitides (group I) compared with secondary vasculitides (group II). Anti-ATP synthase reactivity from group I patients was restricted to the β-subunit of ATP synthase, whereas those from group II was directed to the α-, β- and γ-subunits. Cell surface ATP synthase regulates intracellular pH (pHi). In low extracellular pH medium, we detected abnormal decreased of EC pHi in the presence of anti-ATP synthase antibodies, irrespective of their fine reactivities. Interestingly, soluble hsp60 abrogated the anti-ATP synthase-induced pHi down-regulation. CONCLUSIONS/SIGNIFICANCE: Our results indicate that ATP synthase is targeted by AECAs on the surface of EC that induce intracellular acidification. Such pathogenic effect in vasculitides can be modulated by hsp60 binding on ATP synthase which preserves ATP synthase activity.

Indexed as

AdultAgedAntigens, SurfaceAutoantibodiesAutoimmune DiseasesCase-Control StudiesCells, CulturedChaperonin 60Endothelial CellsFemaleHumansMaleMiddle AgedMitochondrial Proton-Translocating ATPasesVasculitisYoung Adultanti-endothelial cell antibodyAntigens, SurfaceAutoantibodiesChaperonin 60Mitochondrial Proton-Translocating ATPases

Identifiers

PMID21326874
PMCPMC3034716
OpenAlexW2023589003

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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.