Evidence map›Paper›PMID 18502901›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2008

Structural coupling of cardiomyocytes and noncardiomyocytes: quantitative comparisons using a novel micropatterned cell pair assay.

Dawn M Pedrotty, Rebecca Y Klinger, Nima Badie, Sara Hinds, Ara Kardashian, Nenad Bursac

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
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

41 citing papers in PubMed.

  1. Review
  2. Implications for neutrophils in cardiac arrhythmias.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  3. Article
  4. Human brain microvascular endothelial cell pairs model tissue-level blood-brain barrier function.Integrative biology : quantitative biosciences from nano to macro · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Considerations for anFrontiers in pharmacology · 2019
    Review
  9. GAmerican journal of physiology. Heart and circulatory physiology · 2017
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Cellular Communications in the Heart.Cardiac failure review · 2015
    Article
  15. Improved conduction and increased cell retention in healed MI using mesenchymal stem cells suspended in alginate hydrogel.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2014
    Article
  16. Review
  17. Cell-based delivery of dATP via gap junctions enhances cardiac contractility.Journal of molecular and cellular cardiology · 2014
    Article
  18. Article
  19. 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.

Dawn M PedrottyDept. of Biomedical Engineering, Duke Univ., Durham, NC 27708, USA.
Rebecca Y Klinger
Nima Badie
Sara Hinds
Ara Kardashian
Nenad Bursac

Funding

Cellular Cardiomyoplasty in Vitro: Host-Donor Cell InteractionsR21HL083342 · NHLBI · DUKE UNIVERSITY · PI BURSAC, NENAD · 2006 to 2007
$414k
NHLBI NIH HHS HL083342NHLBI NIH HHS R21 HL083342
6 · The paper itself

Abstract

Well-controlled studies of the structural and functional interactions between cardiomyocytes and other cells are essential for understanding heart pathophysiology and for the further development of safe and efficient cell therapies. We established a novel in vitro assay composed of a large number of individual micropatterned cell pairs with reproducible shape, size, and region of cell-cell contact. This assay was applied to quantify and compare the frequency of expression and distribution of electrical (connexin43) and mechanical (N-cadherin) coupling proteins in 5,000 cell pairs made of cardiomyocytes (CMs), cardiac fibroblasts (CFs), skeletal myoblasts (SKMs), and mesenchymal stem cells (MSCs). We found that for all cell pair types, side-side contacts between two cells formed 4.5-14.3 times more often than end-end contacts. Both connexin43 and N-cadherin were expressed in all homotypic CM pairs but in only 13.4-91.6% of pairs containing noncardiomyocytes, where expression was either junctional (at the site of cell-cell contact) or diffuse (inside the cytoplasm). CM expression was exclusively junctional in homotypic pairs but predominantly diffuse in heterotypic pairs. Noncardiomyocyte homotypic pairs exhibited diffuse expression 1.7-8.7 times more often than junctional expression, which was increased 2.6-4.4 times in heterotypic pairs. Junctional connexin43 and N-cadherin expression, respectively, were found in 38.6 +/- 7.3 and 39.6 +/- 6.2% of CM-MSC pairs, 21.9 +/- 5.0 and 13.6 +/- 1.9% of CM-SKM pairs, and in only 3.8-9.6% of CM-CF pairs. Measured frequencies of protein expression and distribution were stable for at least 4 days. Described studies in micropatterned cell pairs shed new light on cellular interactions relevant for cardiac function and cell therapies.

Indexed as

Biological AssayCell CommunicationAnimalsAnimals, NewbornCadherinsCell AdhesionCells, CulturedCell ShapeCoculture TechniquesConnexin 43CytoplasmFibroblastsIntercellular JunctionsMesenchymal Stem CellsMyoblasts, SkeletalMyocytes, CardiacCadherinsConnexin 43

Identifiers

PMID18502901
PMCPMC2494763

What OpenQuestion holds

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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.