Evidence map›Paper›PMID 23649627›Full record

ArticleThe Journal of biological chemistry2013

Adenylyl cyclase anchoring by a kinase anchor protein AKAP5 (AKAP79/150) is important for postsynaptic β-adrenergic signaling.

Mingxu Zhang, Tommaso Patriarchi, Ivar S Stein, Hai Qian, Lucas Matt, Minh Nguyen, Yang K Xiang, Johannes W Hell

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

46 citing papers in PubMed, 66 citations in OpenAlex.

  1. Signaling by intracellular βCell reports · 2025
    Article
  2. Article
  3. Review
  4. Mechanisms of Vascular CaHandbook of experimental pharmacology · 2023
    Article
  5. The CaNeuropharmacology · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. βAnnual review of pharmacology and toxicology · 2020
    Review
  16. Phosphorylation-Dependent Regulation of CaFrontiers in synaptic neuroscience · 2020
    Article
  17. Review
  18. Review
  19. Article
  20. Regulation of ICells · 2019
    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

8 authors at 2 institutions in 1 country.

Mingxu ZhangDepartment of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.
Tommaso Patriarchi
Ivar S Stein
Hai Qian
Lucas Matt
Minh Nguyen
Yang K Xiang
Johannes W Hell
University of California, Davis · USUniversity of Iowa · US

Funding

Subcellular Localization of Cav1.2 by alpha-actininR01AG017502 · NIA · UNIVERSITY OF WISCONSIN MADISON · PI HELL, JOHANNES W · 2000 to 2011
$3.3M
Signaling by cAMP within postsynaptic nano domains R01NS078792R01NS078792 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2016
$2.0M
Subcellular Localization of Cav1.2 by a-actininR56AG017502 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2015 to 2015
$381k
NIA NIH HHS AG017502NIA NIH HHS R01 AG017502NIA NIH HHS R56 AG017502NINDS NIH HHS NS078792NINDS NIH HHS R01 NS078792
6 · The paper itself

Abstract

Recent evidence indicates that the A kinase anchor protein AKAP5 (AKAP79/150) interacts not only with PKA but also with various adenylyl cyclase (AC) isoforms. However, the physiological relevance of AC-AKAP5 binding is largely unexplored. We now show that postsynaptic targeting of AC by AKAP5 is important for phosphorylation of the AMPA-type glutamate receptor subunit GluA1 on Ser-845 by PKA and for synaptic plasticity. Phosphorylation of GluA1 on Ser-845 is strongly reduced (by 70%) under basal conditions in AKAP5 KO mice but not at all in D36 mice, in which the PKA binding site of AKAP5 (i.e. the C-terminal 36 residues) has been deleted without affecting AC association with GluA1. The increase in Ser-845 phosphorylation upon β-adrenergic stimulation is much more severely impaired in AKAP5 KO than in D36 mice. In parallel, long term potentiation induced by a 5-Hz/180-s tetanus, which mimics the endogenous θ-rhythm and depends on β-adrenergic stimulation, is only modestly affected in acute forebrain slices from D36 mice but completely abrogated in AKAP5 KO mice. Accordingly, anchoring of not only PKA but also AC by AKAP5 is important for regulation of postsynaptic functions and specifically AMPA receptor activity.

Indexed as

Synaptic TransmissionAdenylyl CyclasesAdrenergic beta-AgonistsAdrenergic beta-AntagonistsA Kinase Anchor ProteinsAnimalsCyclic AMP-Dependent Protein KinasesHippocampusIsoproterenolLong-Term PotentiationMiceMice, Inbred C57BLMice, KnockoutPhosphorylationPost-Synaptic DensityPropranololadenylyl cyclase 6Adenylyl Cyclasesadenylyl cyclase type VAdrenergic beta-AgonistsAdrenergic beta-AntagonistsAkap5 protein, mouseA Kinase Anchor ProteinsCyclic AMP-Dependent Protein Kinasesglutamate receptor ionotropic, AMPA 2IsoproterenolPropranololProtein SubunitsReceptors, Adrenergic, beta-2Receptors, AMPAAdenylate Cyclase (Adenylyl Cyclase)Adrenergic ReceptorAkapGlutamate Receptors Ionotropic (AMPA, NMDA)Long Term PotentiationProtein Kinase A (PKA)

Identifiers

PMID23649627
PMCPMC3682589
OpenAlexW2086181854

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.