Evidence map›Paper›PMID 37239845›Full record

ArticleInternational journal of molecular sciences2023

GPR19 Coordinates Multiple Molecular Aspects of Stress Responses Associated with the Aging Process.

Stuart Maudsley, Claudia Schrauwen, İrem Harputluoğlu, Deborah Walter, Hanne Leysen, Patricia McDonald

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
0.2field-weighted citation impact, top 55% 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, 1 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 2 countries.

Stuart MaudsleyReceptor Biology Lab, University of Antwerp, 2610 Antwerpen, Belgium.ORCID 0000-0002-1868-184X
Claudia SchrauwenReceptor Biology Lab, University of Antwerp, 2610 Antwerpen, Belgium.ORCID 0000-0003-1807-6428
İrem HarputluoğluReceptor Biology Lab, University of Antwerp, 2610 Antwerpen, Belgium.ORCID 0000-0002-7752-7455
Deborah WalterReceptor Biology Lab, University of Antwerp, 2610 Antwerpen, Belgium.
Hanne LeysenReceptor Biology Lab, University of Antwerp, 2610 Antwerpen, Belgium.ORCID 0000-0002-5852-9033
Patricia McDonaldMoffitt Cancer Center, Department of Metabolism & Physiology, 12902 Magnolia Drive, Tampa, FL 33612, USA.
University of Antwerp · BEMoffitt Cancer Center · US

Funding

Research Foundation - Flanders 1198020NResearch Foundation - Flanders 42/FA010100/32/6484
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) play a significant role in controlling biological paradigms such as aging and aging-related disease. We have previously identified receptor signaling systems that are specifically associated with controlling molecular pathologies associated with the aging process. Here, we have identified a pseudo-orphan GPCR, G protein-coupled receptor 19 (GPR19), that is sensitive to many molecular aspects of the aging process. Through an in-depth molecular investigation process that involved proteomic, molecular biological, and advanced informatic experimentation, this study found that the functionality of GPR19 is specifically linked to sensory, protective, and remedial signaling systems associated with aging-related pathology. This study suggests that the activity of this receptor may play a role in mitigating the effects of aging-related pathology by promoting protective and remedial signaling systems. GPR19 expression variation demonstrates variability in the molecular activity in this larger process. At low expression levels in HEK293 cells, GPR19 expression regulates signaling paradigms linked with stress responses and metabolic responses to these. At higher expression levels, GPR19 expression co-regulates systems involved in sensing and repairing DNA damage, while at the highest levels of GPR19 expression, a functional link to processes of cellular senescence is seen. In this manner, GPR19 may function as a coordinator of aging-associated metabolic dysfunction, stress response, DNA integrity management, and eventual senescence.

Indexed as

ProteomicsSignal TransductionAgingCellular SenescenceHEK293 CellsHumansNerve Tissue ProteinsReceptors, G-Protein-CoupledReceptors, NeurotransmitterGPR19 protein, humanNerve Tissue ProteinsReceptors, G-Protein-CoupledReceptors, NeurotransmitteradiposityagingdamageDNAGPR19longevitymetabolismmitochondriareceptorstress

Identifiers

PMID37239845
PMCPMC10218176
OpenAlexW4378515532

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.