Evidence map›Paper›PMID 19486903›Full record

ArticleJournal of molecular and cellular cardiology2010

Connexin40 and connexin43 determine gating properties of atrial gap junction channels.

Xianming Lin, Joanna Gemel, Aaron Glass, Christian W Zemlin, Eric C Beyer, Richard D Veenstra

Abstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  8. Structure and Functions of Gap Junctions and Their Constituent Connexins in the Mammalian CNS.Biochemistry (Moscow) Supplement. Series A, Membrane and cell biology · 2021
    Article
  9. Article
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  12. Review
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  15. Article
  16. Article
  17. Article
  18. Acetylation mediates Cx43 reduction caused by electrical stimulation.Journal of molecular and cellular cardiology · 2015
    Article
  19. Connexin40 abnormalities and atrial fibrillation in the human heart.Journal of molecular and cellular cardiology · 2014
    Article
  20. 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

6 authors at 2 institutions in 1 country.

Xianming LinDepartment of Pharmacology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210, USA.
Joanna Gemel
Aaron Glass
Christian W Zemlin
Eric C Beyer
Richard D Veenstra
SUNY Upstate Medical University · USUniversity of Chicago · US

Funding

CONNEXONS IN CARDIOVASCULAR CELL COMMUNICATIONR01HL059199 · NHLBI · UNIVERSITY OF CHICAGO · PI BEYER, ERIC C · 1998 to 2013
$3.9M
GAP JUNCTIONS AND IONIC CURRENTS IN DEVELOPING HEARTR01HL042220 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI VEENSTRA, RICHARD DAVID, YANG, JENNY J. · 1988 to 2013
$3.1M
INTERCELLULAR COMMUNICATION IN THE HEARTR01HL045466 · NHLBI · WASHINGTON UNIVERSITY · PI BEYER, ERIC C · 1990 to 2003
$1.4M
NHLBI NIH HHS HL-42220NHLBI NIH HHS HL-59199NHLBI NIH HHS R01 HL042220NHLBI NIH HHS R01 HL045466NHLBI NIH HHS R01 HL059199
6 · The paper itself

Abstract

While ventricular gap junctions contain only Cx43, atrial gap junctions contain both Cx40 and Cx43; yet the functional consequences of this co-expression remain poorly understood. We quantitated the expression of Cx40 and Cx43 and their contributions to atrial gap junctional conductance (g(j)). Neonatal murine atrial myocytes showed similar abundances of Cx40 and Cx43 proteins, while ventricular myocytes contained at least 20 times more Cx43 than Cx40. Since Cx40 gap junction channels are blocked by 2 mM spermine while Cx43 channels are unaffected, we used spermine block as a functional dual whole cell patch clamp assay to determine Cx40 contributions to cardiac g(j). Slightly more than half of atrial g(j) and <or=20% of ventricular g(j) were inhibited. In myocytes from Cx40 null mice, the inhibition of ventricular g(j) was completely abolished, and the block of atrial g(j) was reduced to <20%. Compared to ventricular gap junctions, the transjunctional voltage (V(j))-dependent inactivation of atrial g(j) was reduced and kinetically slowed, while the V(j)-dependence of fast and slow inactivation was unchanged. We conclude that Cx40 and Cx43 are equally abundant in atrium and make similar contributions to atrial g(j). Co-expression of Cx40 accounts for most, but not all, of the differences in the V(j)-dependent gating properties between atrium and ventricle that may play a role in the genesis of slow myocardial conduction and arrhythmias.

Indexed as

AnimalsAnimals, NewbornCell LineCells, CulturedConnexin 43ConnexinsElectrophysiologyGap JunctionsHeart AtriaImmunoblottingImmunohistochemistryIon ChannelsMiceMice, Inbred C57BLMicroscopy, FluorescenceMyocytes, CardiacConnexin 43ConnexinsIon ChannelsSpermine

Identifiers

PMID19486903
PMCPMC2813328
OpenAlexW1978634139

What OpenQuestion holds

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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.