Evidence map›Paper›PMID 28586439›Full record

ArticleEndocrinology2017

RAMP2 Influences Glucagon Receptor Pharmacology via Trafficking and Signaling.

Jaimini Cegla, Ben J Jones, James V Gardiner, David J Hodson, Thomas Marjot, Emma R McGlone, Tricia M Tan, Stephen R Bloom

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Functional modulation of PTH1R activation and signaling by RAMP2.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. RAMP3 determines rapid recycling of atypical chemokine receptor-3 for guided angiogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Glucagon Receptor Signaling and Glucagon Resistance.International journal of molecular sciences · 2019
    Review
  19. 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

8 authors at 2 institutions in 1 country.

Jaimini CeglaDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
Ben J JonesDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
James V GardinerDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
David J HodsonInstitute of Metabolism and Systems Research, University of Birmingham, Edgbaston B15 2TT, United Kingdom.
Thomas MarjotDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
Emma R McGloneDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
Tricia M TanDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
Stephen R BloomDivision of Diabetes, Endocrinology and Metabolism, Imperial College London W12 0NN, United Kingdom.
Imperial College London · GBUniversity of Nottingham · GB

Funding

Department of Health EME/13/121/07Medical Research Council G0502025Medical Research Council G0802390Medical Research Council G1000474Medical Research Council MR/J010731/1Medical Research Council MR/K02115X/1Medical Research Council MR/K023667/1Medical Research Council MR/L013088/1Medical Research Council MR/N00275X/1Medical Research Council MR/P01870X/1Wellcome Trust
6 · The paper itself

Abstract

Endogenous satiety hormones provide an attractive target for obesity drugs. Glucagon causes weight loss by reducing food intake and increasing energy expenditure. To further understand the cellular mechanisms by which glucagon and related ligands activate the glucagon receptor (GCGR), we investigated the interaction of the GCGR with receptor activity modifying protein (RAMP)2, a member of the family of receptor activity modifying proteins. We used a combination of competition binding experiments, cell surface enzyme-linked immunosorbent assay, functional assays assessing the Gαs and Gαq pathways and β-arrestin recruitment, and small interfering RNA knockdown to examine the effect of RAMP2 on the GCGR. Ligands tested were glucagon; glucagonlike peptide-1 (GLP-1); oxyntomodulin; and analog G(X), a GLP-1/glucagon coagonist developed in-house. Confocal microscopy was used to assess whether RAMP2 affects the subcellular distribution of GCGR. Here we demonstrate that coexpression of RAMP2 and the GCGR results in reduced cell surface expression of the GCGR. This was confirmed by confocal microscopy, which demonstrated that RAMP2 colocalizes with the GCGR and causes significant GCGR cellular redistribution. Furthermore, the presence of RAMP2 influences signaling through the Gαs and Gαq pathways, as well as recruitment of β-arrestin. This work suggests that RAMP2 may modify the agonist activity and trafficking of the GCGR, with potential relevance to production of new peptide analogs with selective agonist activities.

Indexed as

Animalsbeta-ArrestinsCalciumCHO CellsCricetinaeCricetulusDNAGene Expression RegulationGlucagonHEK293 CellsHumansProtein BindingProtein TransportReceptor Activity-Modifying Protein 2Receptors, GlucagonRNA Interferencebeta-ArrestinsCalciumDNAGlucagonRAMP2 protein, humanReceptor Activity-Modifying Protein 2Receptors, GlucagonRNA, Small Interfering

Identifiers

PMID28586439
PMCPMC5551549
OpenAlexW2622192206

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.