Evidence map›Paper›PMID 29855662›Full record

ArticleCellular and molecular life sciences : CMLS2018

The adhesion receptor GPR56 is activated by extracellular matrix collagen III to improve β-cell function.

Oladapo E Olaniru, Attilio Pingitore, Stefanie Giera, Xianhua Piao, Ramón Castañera González, Peter M Jones, Shanta J Persaud

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2018. 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
6.6field-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

36 citing papers in PubMed, 58 citations in OpenAlex.

  1. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
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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 3 countries.

Oladapo E OlaniruDepartment of Diabetes, School of Life Course Sciences, King's College London, Guy's Campus, London, SE1 1UL, UK.ORCID http://orcid.org/0000-0001-6830-2353
Attilio PingitoreDepartment of Diabetes, School of Life Course Sciences, King's College London, Guy's Campus, London, SE1 1UL, UK.
Stefanie GieraDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA, 02115, USA.
Xianhua PiaoDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA, 02115, USA.
Ramón Castañera GonzálezDepartment of General Surgery, Rio Carrión Hospital, University Hospital Complex of Palencia, Palencia, Spain.
Peter M JonesDepartment of Diabetes, School of Life Course Sciences, King's College London, Guy's Campus, London, SE1 1UL, UK.
Shanta J PersaudDepartment of Diabetes, School of Life Course Sciences, King's College London, Guy's Campus, London, SE1 1UL, UK. shanta.persaud@kcl.ac.uk.ORCID http://orcid.org/0000-0002-4933-5958
King's College London · GBBoston Children's Hospital · USHospital Rio Carrion · ES

Funding

Diabetes UK 17/0005600European Foundation for the Study of Diabetes Albert Renold Travel FellowshipSociety for Endocrinology Early Career Grant
6 · The paper itself

Abstract

aimsG-protein coupled receptor 56 (GPR56) is the most abundant islet-expressed G-protein coupled receptor, suggesting a potential role in islet function. This study evaluated islet expression of GPR56 and its endogenous ligand collagen III, and their effects on β-cell function.

methodsGPR56 and collagen III expression in mouse and human pancreas sections was determined by fluorescence immunohistochemistry. Effects of collagen III on β-cell proliferation, apoptosis, intracellular calcium ([Ca

resultsImmunostaining of mouse and human pancreases revealed that GPR56 was expressed by islet β-cells while collagen III was confined to the peri-islet basement membrane and islet capillaries. Collagen III protected β-cells from cytokine-induced apoptosis, triggered increases in [Ca

conclusionWe have demonstrated that collagen III improves islet function by increasing insulin secretion and protecting against apoptosis. Our data suggest that collagen III may be effective in optimising islet function to improve islet transplantation outcomes, and GPR56 may be a target for the treatment of type 2 diabetes.

Indexed as

AnimalsApoptosisCalciumCell ProliferationCollagenDiabetes Mellitus, Type 2Extracellular MatrixGene Expression RegulationHumansInsulin-Secreting CellsIslets of LangerhansMiceMice, KnockoutPancreasReceptors, G-Protein-CoupledADGRG1 protein, humanAdgrg1 protein, mouseCalciumCollagenReceptors, G-Protein-CoupledCalciumCollagen IIIExtracellular matrixGPR56Insulin secretionIslets

Identifiers

PMID29855662
PMCPMC6182347
OpenAlexW2805281779

What OpenQuestion holds

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LicenceCC BY
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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.