Evidence map›Paper›PMID 25143405›Full record

ArticleMolecular biology of the cell2014

Arrestins function in cAR1 GPCR-mediated signaling and cAR1 internalization in the development of Dictyostelium discoideum.

Xiumei Cao, Jianshe Yan, Shi Shu, Joseph A Brzostowski, Tian Jin

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Two endogenousProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. From environmental sensing to developmental control: cognitive evolution in dictyostelid social amoebas.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  4. Review
  5. Decoding the chemotactic signal.Journal of leukocyte biology · 2018
    Review
  6. Article
  7. G-Protein Dependent Signal Transduction and Ubiquitination in Dictyostelium.International journal of molecular sciences · 2017
    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

5 authors at 2 institutions in 2 countries.

Xiumei CaoShanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Jianshe YanShanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China Chemotaxis Signal Section, Laboratory of Immunogenetics, National Institutes of Health, Rockville, MD 20852 tjin@niaid.nih.gov yanjianshe@sjtu.edu.cn.
Shi ShuLaboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.
Joseph A BrzostowskiLaboratory of Immunogenetics Imaging Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Tian JinChemotaxis Signal Section, Laboratory of Immunogenetics, National Institutes of Health, Rockville, MD 20852 tjin@niaid.nih.gov yanjianshe@sjtu.edu.cn.
National Institutes of Health · USShanghai Jiao Tong University · CN

Funding

The mechanisms underlying the GPCR-mediated chemotaxis in D. discoideumZIAAI000916 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI JIN, TIAN · 2009 to 2025
$12.3M
Intramural NIH HHS
6 · The paper itself

Abstract

Oscillation of chemical signals is a common biological phenomenon, but its regulation is poorly understood. At the aggregation stage of Dictyostelium discoideum development, the chemoattractant cAMP is synthesized and released at 6-min intervals, directing cell migration. Although the G protein-coupled cAMP receptor cAR1 and ERK2 are both implicated in regulating the oscillation, the signaling circuit remains unknown. Here we report that D. discoideum arrestins regulate the frequency of cAMP oscillation and may link cAR1 signaling to oscillatory ERK2 activity. Cells lacking arrestins (adcB(-)C(-)) display cAMP oscillations during the aggregation stage that are twice as frequent as for wild- type cells. The adcB(-)C(-) cells also have a shorter period of transient ERK2 activity and precociously reactivate ERK2 in response to cAMP stimulation. We show that arrestin domain-containing protein C (AdcC) associates with ERK2 and that activation of cAR1 promotes the transient membrane recruitment of AdcC and interaction with cAR1, indicating that arrestins function in cAR1-controlled periodic ERK2 activation and oscillatory cAMP signaling in the aggregation stage of D. discoideum development. In addition, ligand-induced cAR1 internalization is compromised in adcB(-)C(-) cells, suggesting that arrestins are involved in elimination of high-affinity cAR1 receptors from cell surface after the aggregation stage of multicellular development.

Indexed as

ArrestinsDictyosteliumMitogen-Activated Protein Kinase 1PhosphorylationReceptors, Cyclic AMPReceptors, G-Protein-CoupledSignal TransductionArrestinsMitogen-Activated Protein Kinase 1Receptors, Cyclic AMPReceptors, G-Protein-Coupled

Identifiers

PMID25143405
PMCPMC4196870
OpenAlexW2170828577

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.