Evidence map›Paper›PMID 24324269›Full record

ArticleThe Journal of biological chemistry2014

Sorting of β1-adrenergic receptors is mediated by pathways that are either dependent on or independent of type I PDZ, protein kinase A (PKA), and SAP97.

Mohammed M Nooh, Maryanne M Chumpia, Thomas B Hamilton, Suleiman W Bahouth

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  9. Novel Paradigms GoverningMolecular pharmacology · 2018
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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

4 authors at 2 institutions in 2 countries.

Mohammed M NoohFrom the Department of Pharmacology, University of Tennessee Health Sciences Center, Memphis, Tennessee 38163 and.
Maryanne M Chumpia
Thomas B Hamilton
Suleiman W Bahouth
University of Tennessee Health Science Center · USCairo University · EG

Funding

CORE--MOLECULAR BIOLOGYP30EY013080 · NEI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI JOHNSON, DIANNA AMMONS · 2000 to 2010
$3.7M
PKA targeting: A novel mechanism for GPCR resensitizationR01HL085848 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI BAHOUTH, SULEIMAN WAKIM · 2009 to 2012
$1.5M
NEI NIH HHS 5P30EY13080-10NEI NIH HHS P30 EY013080NHLBI NIH HHS HL-085848NHLBI NIH HHS R01 HL085848
6 · The paper itself

Abstract

The β1-adrenergic receptor (β1-AR) is a target for treatment of major cardiovascular diseases, such as heart failure and hypertension. Recycling of agonist-internalized β1-AR is dependent on type I PSD-95/DLG/ZO1 (PDZ) in the C-tail of the β1-AR and on protein kinase A (PKA) activity (Gardner, L. A., Naren, A. P., and Bahouth, S. W. (2007) J. Biol. Chem. 282, 5085-5099). We explored the effects of point mutations in the PDZ and in the activity of PKA on recycling of the β1-AR and its binding to the PDZ-binding protein SAP97. These studies indicated that β1-AR recycling was inhibited by PKA inhibitors and by mutations in the PDZ that interfered with SAP97 binding. The trafficking effects of short sequences differing in PDZ and SAP97 binding were examined using chimeric mutant β1-AR. β1-AR chimera containing the type I PDZ of the β2-adrenergic receptor that does not bind to SAP97 failed to recycle except when serine 312 was mutated to aspartic acid. β1-AR chimera with type I PDZ sequences from the C-tails of aquaporin-2 or GluR1 recycled in a SAP97- and PKA-dependent manner. Non-PDZ β1-AR chimera derived from μ-opioid, dopamine 1, or GluR2 receptors promoted rapid recycling of chimeric β1-AR in a SAP97- and PKA-independent manner. Moreover, the nature of the residue at position -3 in the PDZ regulated whether the β1-AR was internalized alone or in complex with SAP97. These results indicate that divergent pathways were involved in trafficking the β1-AR and provide a roadmap for its trafficking via type I PDZs versus non-PDZs.

Indexed as

Adaptor Proteins, Signal TransducingCyclic AMP-Dependent Protein KinasesDiscs Large Homolog 1 ProteinHEK293 CellsHumansMembrane ProteinsProtein Structure, TertiaryProtein TransportReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Receptors, AMPARecombinant Fusion ProteinsAdaptor Proteins, Signal TransducingCyclic AMP-Dependent Protein KinasesDiscs Large Homolog 1 ProteinDLG1 protein, humanglutamate receptor ionotropic, AMPA 2Membrane ProteinsReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Receptors, AMPARecombinant Fusion ProteinsAdrenergic ReceptorConfocal MicroscopyG Protein-coupled Receptor (GPCR)Protein Kinase A (PKA)Trafficking

Identifiers

PMID24324269
PMCPMC3900972
OpenAlexW2063795338

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.