Evidence map›Paper›PMID 21911612›Full record

ArticleThe Journal of physiology2011

Postsynaptic density-95 scaffolding of Shaker-type K⁺ channels in smooth muscle cells regulates the diameter of cerebral arteries.

Biny K Joseph, Keshari M Thakali, Asif R Pathan, Eunju Kang, Nancy J Rusch, Sung W Rhee

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. KMicrocirculation (New York, N.Y. : 1994) · 2018
    Review
  7. Molecular determinants of beta-adrenergic signaling to voltage-gated KMicrocirculation (New York, N.Y. : 1994) · 2018
    Review
  8. Article
  9. Article
  10. Beta1-adrenergic receptor-mediated dilation of rat cerebral artery requires Shaker-type KV1 channels on PSD95 scaffold.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    Article
  11. Article
  12. Review
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Biny K JosephDepartment of Pharmacology and Toxicology, College of Medicine, The University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Keshari M Thakali
Asif R Pathan
Eunju Kang
Nancy J Rusch
Sung W Rhee
University of Arkansas for Medical Sciences · US

Funding

PSD95 scaffolding of vascular K+ channels in hypertensionR01HL097107 · NHLBI · UNIV OF ARKANSAS FOR MED SCIS · PI RHEE, SUNG W · 2010 to 2014
$1.8M
Role of Cerebrovascular K+ Channels in HypertensionR01HL059238 · NHLBI · UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK · PI RUSCH, NANCY J · 1998 to 2005
$1.8M
L-type calcium channels are silent during depolarization of venous smooth muscleF32HL095284 · NHLBI · UNIV OF ARKANSAS FOR MED SCIS · PI THAKALI, KESHARI · 2009 to 2011
$146k
NHLBI NIH HHS F32 HL095284NHLBI NIH HHS R01 HL059238NHLBI NIH HHS R01 HL097107
6 · The paper itself

Abstract

Postsynaptic density-95 (PSD95) is a 95 kDa scaffolding molecule in the brain that clusters postsynaptic proteins including ion channels, receptors, enzymes and other signalling partners required for normal cognition. The voltage-gated, Shaker-type K(+) (K(V)1) channel is one key binding partner of PSD95 scaffolds in neurons. However, K(V)1 channels composed of α1.2 and α1.5 pore-forming subunits also are expressed in the vascular smooth muscle cells (cVSMCs) of the cerebral circulation, although the identity of their molecular scaffolds is unknown. Since α1.2 contains a binding motif for PSD95, we explored the possibility that cVSMCs express PSD95 as a scaffold to promote K(V)1 channel expression and cerebral vasodilatation. Cerebral arteries from Sprague-Dawley rats were isolated for analysis of PSD95 and K(V)1 channel proteins. PSD95 was detected in cVSMCs and it co-immunoprecipitated and co-localized with the pore-forming α1.2 subunit of the K(V)1 channel. Antisense-mediated knockdown of PSD95 profoundly reduced K(V)1 channel expression and suppressed K(V)1 current in patch-clamped cVSMCs. Loss of PSD95 also depolarized cVSMCs in pressurized cerebral arteries and induced a strong constriction associated with a loss of functional K(V)1 channels. Our findings provide initial evidence that PSD95 is expressed in cVSMCs, and the K(V)1 channel is one of its important binding partners. PSD95 appears to function as a critical 'dilator' scaffold in cerebral arteries by increasing the number of functional K(V)1 channels at the plasma membrane.

Indexed as

VasodilationAnimalsBlotting, WesternCerebral ArteriesDisks Large Homolog 4 ProteinFurocoumarinsGene Knockdown TechniquesIntracellular Signaling Peptides and ProteinsMaleMembrane PotentialsMembrane ProteinsMyocytes, Smooth MuscleOligonucleotides, AntisensePatch-Clamp TechniquesPost-Synaptic DensityPotassium Channel BlockersDisks Large Homolog 4 ProteinDlg4 protein, ratFurocoumarinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsOligonucleotides, AntisensePotassium Channel BlockersShaker Superfamily of Potassium ChannelsSpider Venoms

Identifiers

PMID21911612
PMCPMC3225670
OpenAlexW1545049773

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.