Evidence map›Paper›PMID 27226565›Full record

ArticleThe Journal of biological chemistry2016

The α-Arrestin ARRDC3 Regulates the Endosomal Residence Time and Intracellular Signaling of the β2-Adrenergic Receptor.

Xufan Tian, Roshanak Irannejad, Shanna L Bowman, Yang Du, Manojkumar A Puthenveedu, Mark von Zastrow, Jeffrey L Benovic

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Class A and B GPCRs trigger rapid GαCommunications biology · 2025
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  6. Signaling by intracellular βCell reports · 2025
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  9. 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
  10. Review
  11. Article
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  14. cAMP signaling: a remarkably regional affair.Trends in biochemical sciences · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Thioredoxin-Interacting Protein in Cancer and Diabetes.Antioxidants & redox signaling · 2022
    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

7 authors at 4 institutions in 1 country.

Xufan TianFrom the Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Roshanak Irannejadthe Department of Psychiatry, University of California at San Francisco, San Francisco, California 94158.
Shanna L Bowmanthe Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, and.
Yang Duthe Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, California 94305.
Manojkumar A Puthenveeduthe Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, and.
Mark von Zastrowthe Department of Psychiatry, University of California at San Francisco, San Francisco, California 94158.
Jeffrey L BenovicFrom the Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, jeffrey.benovic@jefferson.edu.
Carnegie Mellon University · USThomas Jefferson University · USUniversity of California, San Francisco · USStanford University · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
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
Predoctorial Training in Basic NeuroscienceT32NS007433 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MERINEY, STEPHEN D · 1998 to 2022
$8.0M
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
Role of Arrestins in G Protein-Coupled Receptor RegulationR37GM047417 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BENOVIC, JEFFREY L · 2006 to 2015
$4.3M
MECHANISMS ENSURING SEQUENCE-DEPENDENT GPCR RECYCLINGR01GM117425 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 2016 to 2020
$1.5M
Arrestin Interaction with Endocytic ComponentsR01GM068857 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BENOVIC, JEFFREY L · 2003 to 2006
$1.3M
Role of endocytosis in beta-adrenergic receptors signaling in cardiomyocytesR00HL122508 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI IRANNEJAD, ROSHANAK · 2017 to 2019
$747k
TRAFFICKING AND FUNCTION OF MU-OPIOD RECEPTOR GENETIC VARIANTSR21DA036086 · NIDA · CARNEGIE-MELLON UNIVERSITY · PI PUTHENVEEDU, MANOJKUMAR A · 2013 to 2014
$371k
Role of endocytosis in beta-adrenergic receptors signaling in cardiomyocytesK99HL122508 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI IRANNEJAD, ROSHANAK · 2014 to 2015
$269k
NCI NIH HHS P30 CA056036NHLBI NIH HHS K99 HL122508NHLBI NIH HHS R00 HL122508NIDA NIH HHS P01 DA010154NIDA NIH HHS R01 DA010711NIDA NIH HHS R01 DA012864NIDA NIH HHS R21 DA036086NIGMS NIH HHS R01 GM068857NIGMS NIH HHS R01 GM117425NIGMS NIH HHS R37 GM047417NINDS NIH HHS T32 NS007433
6 · The paper itself

Abstract

Arrestin domain-containing protein 3 (ARRDC3) is a member of the mammalian α-arrestin family, which is predicted to share similar tertiary structure with visual-/β-arrestins and also contains C-terminal PPXY motifs that mediate interaction with E3 ubiquitin ligases. Recently, ARRDC3 has been proposed to play a role in regulating the trafficking of G protein-coupled receptors, although mechanistic insight into this process is lacking. Here, we focused on characterizing the role of ARRDC3 in regulating the trafficking of the β2-adrenergic receptor (β2AR). We find that ARRDC3 primarily localizes to EEA1-positive early endosomes and directly interacts with the β2AR in a ligand-independent manner. Although ARRDC3 has no effect on β2AR endocytosis or degradation, it negatively regulates β2AR entry into SNX27-occupied endosomal tubules. This results in delayed recycling of the receptor and a concomitant increase in β2AR-dependent endosomal signaling. Thus, ARRDC3 functions as a switch to modulate the endosomal residence time and subsequent intracellular signaling of the β2AR.

Indexed as

ArrestinsEndosomesHEK293 CellsHumansReceptors, Adrenergic, beta-2Signal TransductionARRDC3 protein, humanArrestinsReceptors, Adrenergic, beta-2arrestinarrestin domain-containing protein 3cell signalingendosomal signalingG protein-coupled receptor (GPCR)receptor recyclingtraffickingβ2 adrenergic receptor

Identifiers

PMID27226565
PMCPMC4938174
OpenAlexW2357419851

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.