Evidence map›Paper›PMID 38522808›Full record

ReviewCellular signalling2024

Deciphering the role of glycosaminoglycans in GPCR signaling.

Sofya Savransky, Alex D White, Jean-Pierre Vilardaga

Open access · greenAbstract readReview
In one paragraph

Review in Cellular signalling, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
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

3 authors at 1 institution in 1 country.

Sofya SavranskyDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Graduate Program in Molecular Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA. Electronic address: sos61@pitt.edu.
Alex D WhiteDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Graduate Program in Molecular Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Jean-Pierre VilardagaDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA. Electronic address: jpv@pitt.edu.
University of Pittsburgh · US

Funding

Structure and function of PTH class B GPCRR01DK116780 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Ivet Bahar, Jean-Pierre Vilardaga · 2018 to 2026
$4.2M
Regulation of Parathyroid Functions By G-Protein Coupled ReceptorsR01DK122259 · NIDDK · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI CHANG, WENHAN, VILARDAGA, JEAN-PIERRE · 2019 to 2023
$2.2M
Predoctoral Training in Pharmacological Sciences (Resubmission)T32GM133332 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Tija C. Jacob, Francisco Jose Schopfer · 2020 to 2026
$1.8M
Identification of selective inhibitors of PTH-receptor for Jansen’s metaphyseal chondrodysplasiaR21DE032478 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TABOAS, JUAN MANUEL, VILARDAGA, JEAN-PIERRE · 2022 to 2023
$433k
The role of cell surface glycosaminoglycans (GAGs) in PTHrP bias signalingF31DK136222 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SAVRANSKY, SOFYA · 2024 to 2025
$99k
NIDCR NIH HHS R21 DE032478NIDDK NIH HHS F31 DK136222NIDDK NIH HHS R01 DK116780NIDDK NIH HHS R01 DK122259NIGMS NIH HHS T32 GM133332
6 · The paper itself

Abstract

G protein-coupled receptors (GPCR) and glycosaminoglycans (GAGs) are two essential components of the cell surface that regulate physiological processes in the body. GPCRs are the most extensive family of transmembrane receptors that control cellular responses to extracellular stimuli, while GAGs are polysaccharides that contribute to the function of the extracellular matrix (ECM). Due to their proximity to the plasma membrane, GAGs participate in signal transduction by interacting with various extracellular molecules and cell surface receptors. GAGs can directly interact with certain GPCRs or their ligands (chemokines, peptide hormones and neuropeptides, structural proteins, and enzymes) from the glutamate receptor family, the rhodopsin receptor family, the adhesion receptor family, and the secretin receptor family. These interactions have recently become an emerging topic, providing a new avenue for understanding how GPCR signaling is regulated. This review discusses our current state of knowledge about the role of GAGs in GPCR signaling and function.

Indexed as

GlycosaminoglycansReceptors, G-Protein-CoupledCell MembraneRhodopsinSignal TransductionGlycosaminoglycansReceptors, G-Protein-CoupledRhodopsinEndosomal cAMP signalingGlycosaminoglycansGPCRG protein-coupled receptorsPTH-related peptide

Identifiers

PMID38522808
PMCPMC10999332
OpenAlexW4393087560

What OpenQuestion holds

Textmetadata
LicenceTDM
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.