Evidence map›Paper›PMID 24993824›Full record

ArticleThe Journal of biological chemistry2014

The G protein-coupled receptor P2Y14 influences insulin release and smooth muscle function in mice.

Jaroslawna Meister, Diana Le Duc, Albert Ricken, Ralph Burkhardt, Joachim Thiery, Helga Pfannkuche, Tobias Polte, Johannes Grosse, Torsten Schöneberg, Angela Schulz

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Metabolomic Insights Into the Impact of a Maternal Western-Style Diet and Leptin Supplementation During Suckling on Adult Rat Offspring.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Article
  4. P2YActa pharmaceutica Sinica. B · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Exploration of Alternative Scaffolds for P2YJournal of medicinal chemistry · 2020
    Article
  15. P2YACS medicinal chemistry letters · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

10 authors at 3 institutions in 2 countries.

Jaroslawna MeisterFrom the Institute of Biochemistry, Integrated Research and Treatment Center for Adiposity Diseases.
Diana Le DucFrom the Institute of Biochemistry.
Albert RickenInstitute of Anatomy, and.
Ralph BurkhardtInstitute of Laboratory Medicine, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.
Joachim ThieryInstitute of Laboratory Medicine, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.
Helga Pfannkuchethe Institute of Veterinary Physiology, Faculty of Veterinary Medicine, University of Leipzig, 04109 Leipzig, Germany.
Tobias Poltethe Department of Environmental Immunology, UFZ-Helmholtz Centre for Environmental Research Leipzig-Halle, 04318 Leipzig, Germany, the Department of Dermatology, Venerology and Allergology, Leipzig University Medical Center, 04109 Leipzig, Germany, and.
Johannes GrosseTakeda Cambridge Ltd., Cambridge CB4 0PZ, United Kingdom.
Torsten SchönebergFrom the Institute of Biochemistry, schoberg@medizin.uni-leipzig.de.
Angela SchulzFrom the Institute of Biochemistry, Integrated Research and Treatment Center for Adiposity Diseases.
Leipzig University · DEIFB Adiposity Diseases · DETakeda (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

UDP sugars were identified as extracellular signaling molecules, assigning a new function to these compounds in addition to their well defined role in intracellular substrate metabolism and storage. Previously regarded as an orphan receptor, the G protein-coupled receptor P2Y14 (GPR105) was found to bind extracellular UDP and UDP sugars. Little is known about the physiological functions of this G protein-coupled receptor. To study its physiological role, we used a gene-deficient mouse strain expressing the bacterial LacZ reporter gene to monitor the physiological expression pattern of P2Y14. We found that P2Y14 is mainly expressed in pancreas and salivary glands and in subpopulations of smooth muscle cells of the gastrointestinal tract, blood vessels, lung, and uterus. Among other phenotypical differences, knock-out mice showed a significantly impaired glucose tolerance following oral and intraperitoneal glucose application. An unchanged insulin tolerance suggested altered pancreatic islet function. Transcriptome analysis of pancreatic islets showed that P2Y14 deficiency significantly changed expression of components involved in insulin secretion. Insulin secretion tests revealed a reduced insulin release from P2Y14-deficient islets, highlighting P2Y14 as a new modulator of proper insulin secretion.

Indexed as

AnimalsBase SequenceDNA PrimersFemaleGastric EmptyingGlucose IntoleranceInsulinInsulin SecretionIslets of LangerhansMiceMice, KnockoutMuscle, SmoothPolymerase Chain ReactionReceptors, Purinergic P2YDNA PrimersInsulinP2ry14 protein, mouseReceptors, Purinergic P2YGene KnockoutGlucose MetabolismG Protein-coupled Receptor (GPCR)Pancreatic IsletSignal Transduction

Identifiers

PMID24993824
PMCPMC4156089
OpenAlexW2014874593

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.