Evidence map›Paper›PMID 32058960›Full record

ArticleiScience2020

The Proton-Sensing GPR4 Receptor Regulates Paracellular Gap Formation and Permeability of Vascular Endothelial Cells.

Elizabeth A Krewson, Edward J Sanderlin, Mona A Marie, Shayan Nik Akhtar, Juraj Velcicky, Pius Loetscher, Li V Yang

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-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

36 citing papers in PubMed, 52 citations in OpenAlex.

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  16. Inhibition of proton sensor GPR68 suppresses endothelial dysfunction and acute lung injury caused by Staphylococcus aureus bacterial particles.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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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

7 authors at 3 institutions in 2 countries.

Elizabeth A KrewsonDepartment of Anatomy and Cell Biology, East Carolina University, Greenville, NC 27834, USA.
Edward J SanderlinDepartment of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA.
Mona A MarieDepartment of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA.
Shayan Nik AkhtarDepartment of Anatomy and Cell Biology, East Carolina University, Greenville, NC 27834, USA.
Juraj VelcickyNovartis Institutes for BioMedical Research, 4002 Basel, Switzerland.
Pius LoetscherNovartis Institutes for BioMedical Research, 4002 Basel, Switzerland.
Li V YangDepartment of Anatomy and Cell Biology, East Carolina University, Greenville, NC 27834, USA; Department of Internal Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA. Electronic address: yangl@ecu.edu.
East Carolina University · USNovartis Institutes for BioMedical ResearchNovartis (Switzerland) · CH

Funding

Role of the GPR4 Receptor in Intestinal Inflammation and CancerR15DK109484 · NIDDK · EAST CAROLINA UNIVERSITY · PI YANG, LI · 2016 to 2016
$436k
NIDDK NIH HHS R15 DK109484
6 · The paper itself

Abstract

GPR4 is a pH-sensing G protein-coupled receptor highly expressed in vascular endothelial cells and can be activated by protons in the inflamed tissue microenvironment. Herein, we report that acidosis-induced GPR4 activation increases paracellular gap formation and permeability of vascular endothelial cells through the G

Indexed as

Molecular Mechanism of BehaviorPathophysiologySpecialized Functions of Cells

Identifiers

PMID32058960
PMCPMC6997876
OpenAlexW2999329884

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.