Evidence map›Paper›PMID 21157968›Full record

ReviewWorld journal of gastroenterology2010

Ecto-F₁-ATPase: a moonlighting protein complex and an unexpected apoA-I receptor.

Pierre Vantourout, Claudia Radojkovic, Laeticia Lichtenstein, Véronique Pons, Eric Champagne, Laurent O Martinez

Open access · greenAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 67 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

6 authors at 1 institution in 1 country.

Pierre VantouroutInstitut National de la Santé et de la Recherche Médicale U1048, Toulouse F-31000, France.
Claudia Radojkovic
Laeticia Lichtenstein
Véronique Pons
Eric Champagne
Laurent O Martinez
Institut National de Recherche en Santé Publique · ML

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial ATP synthase has been recently detected at the surface of different cell types, where it is a high affinity receptor for apoA-I, the major protein component in high density lipoproteins (HDL). Cell surface ATP synthase (namely ecto-F₁-ATPase) expression is related to different biological effects, such as regulation of HDL uptake by hepatocytes, endothelial cell proliferation or antitumor activity of Vγ9/Vδ2 T lymphocytes. This paper reviews the recently discovered functions and regulations of ecto-F₁-ATPase. Particularly, the role of the F₁-ATPase pathway(s) in HDL-cholesterol uptake and apoA-I-mediated endothelial protection suggests its potential importance in reverse cholesterol transport and its regulation might represent a potential therapeutic target for HDL-related therapy for cardiovascular diseases. Therefore, it is timely for us to better understand how this ecto-enzyme and downstream pathways are regulated and to develop pharmacologic interventions.

Indexed as

Adenosine TriphosphatasesAnimalsApolipoprotein A-ICell SurvivalCholesterolCholesterol, HDLEndothelial CellsHumansLiverMitochondrial Proton-Translocating ATPasesModels, MolecularNeoplasmsAdenosine TriphosphatasesApolipoprotein A-ICholesterolCholesterol, HDLectoATPaseMitochondrial Proton-Translocating ATPases

Identifiers

PMID21157968
PMCPMC3007107
OpenAlexW1511182767

What OpenQuestion holds

Textmetadata
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.