Evidence map›Paper›PMID 25605726›Full record

ReviewThe Journal of biological chemistry2015

G protein-coupled receptor (GPCR) signaling via heterotrimeric G proteins from endosomes.

Nikoleta G Tsvetanova, Roshanak Irannejad, Mark von Zastrow

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
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  5. Review
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  7. Opioid receptors reveal a discrete cellular mechanism of endosomal G protein activation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Review
  10. Review
  11. Article
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  14. Location-biased activation of the proton-sensor GPR65 is uncoupled from receptor trafficking.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Endosomal parathyroid hormone receptor signaling.American journal of physiology. Cell physiology · 2022
    Review

28 more citing papers are in PubMed but not listed here.

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.

Nikoleta G TsvetanovaFrom the Departments of Psychiatry and.
Roshanak IrannejadFrom the Departments of Psychiatry and.
Mark von ZastrowFrom the Departments of Psychiatry and Cellular and Molecular Pharmacology, University of California, San Francisco, California 94158 mark.vonzastrow@ucsf.edu.
University of California, San Francisco · US

Funding

The Presynaptic Vesicle Cycle for the Slow Acting Neurotransmitter SecretionP01DA010154 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EDWARDS, ROBERT H, KREITZER, ANATOL · 1995 to 2016
$14.7M
PROTEINS REGULATING ENDOCYTOSIS OF OPIOID RECEPTORSR01DA012864 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Mark E Von Zastrow · 2000 to 2026
$7.9M
Membrane Trafficking of Opioid and Adrenergic ReceptorsR01DA010711 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VONZASTROW, MARK E · 2014 to 2023
$4.6M
Substituted Amphetamines: NO-Dependent MechanismsR01DA012867 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ITZHAK, YOSSEF · 2001 to 2005
$1.5M
Role of endocytosis in beta-adrenergic receptors signaling in cardiomyocytesK99HL122508 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI IRANNEJAD, ROSHANAK · 2014 to 2015
$269k
NHLBI NIH HHS K99 HL122508NHLBI NIH HHS K99HL122508NIDA NIH HHS P01 DA010154NIDA NIH HHS R01 DA010711NIDA NIH HHS R01DA010711NIDA NIH HHS R01 DA012864NIDA NIH HHS R01 DA012867NIDA NIH HHS R01DA012867
6 · The paper itself

Abstract

Some G protein-coupled receptors (GPCRs), in addition to activating heterotrimeric G proteins in the plasma membrane, appear to elicit a "second wave" of G protein activation after ligand-induced internalization. We briefly summarize evidence supporting this view and then discuss what is presently known about the functional significance of GPCR-G protein activation in endosomes. Endosomal activation can shape the cellular response temporally by prolonging its overall duration, and may shape the response spatially by moving the location of intracellular second messenger production relative to effectors.

Indexed as

Signal TransductionAnimalsBiosensing TechniquesCyclic AMPEndocytosisEndosomesHeterotrimeric GTP-Binding ProteinsHumansReceptors, G-Protein-CoupledCyclic AMPHeterotrimeric GTP-Binding ProteinsReceptors, G-Protein-CoupledCell SignalingCyclic AMP (cAMP)EndocytosisEndosomeG ProteinG Protein-coupled Receptor (GPCR)Protein SortingSignal TransductionTranscription

Identifiers

PMID25605726
PMCPMC4358092
OpenAlexW2012895196

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.