Evidence map›Paper›PMID 22884710›Full record

ArticleProgress in biophysics and molecular biology

Mechanical modulation of the transverse tubular system of ventricular cardiomyocytes.

Thomas G McNary, Kenneth W Spitzer, Hilary Holloway, John H B Bridge, Peter Kohl, Frank B Sachse

Abstract read
In one paragraph

Article in Progress in biophysics and molecular biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Physiological and Pathological Relevance of Selective and Nonselective CaAdvances in experimental medicine and biology · 2021
    Article
  8. Article
  9. Article
  10. Mitochondrial Deformation During the Cardiac Mechanical Cycle.Anatomical record (Hoboken, N.J. : 2007) · 2019
    Article
  11. Dyadic Plasticity in Cardiomyocytes.Frontiers in physiology · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Electron tomography of rabbit cardiomyocyte three-dimensional ultrastructure.Progress in biophysics and molecular biology · 2016
    Article
  16. Rabbit models of cardiac mechano-electric and mechano-mechanical coupling.Progress in biophysics and molecular biology · 2016
    Review
  17. Review
  18. Article
  19. Article
  20. Review
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 3 institutions in 3 countries.

Thomas G McNaryNora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, 95 South 2000 East, Salt Lake City, UT 84112-5000, USA. mcnary@cvrti.utah.edu
Kenneth W Spitzer
Hilary Holloway
John H B Bridge
Peter Kohl
Frank B Sachse
Harrison Medical Center · USImperial College London · GBUniversity of Auckland · NZ

Funding

pH REGULATION IN HEART CELLSR37HL042873 · NHLBI · UNIVERSITY OF UTAH · PI SPITZER, KENNETH W · 2003 to 2012
$2.0M
Remodeling of the Transverse Tubular System and Ryanodine Receptor Clusters in DyR01HL094464 · NHLBI · UNIVERSITY OF UTAH · PI SACHSE, FRANK BERND · 2010 to 2014
$1.9M
British Heart Foundation FS/12/17/29532British Heart Foundation PG/09/031/27221NHLBI NIH HHS R01 HL094464NHLBI NIH HHS R01HL094464NHLBI NIH HHS R37 HL042873NHLBI NIH HHS R37HL042873
6 · The paper itself

Abstract

In most mammalian cardiomyocytes, the transverse tubular system (t-system) is a major site for electrical signaling and excitation-contraction coupling. The t-system consists of membrane invaginations, which are decorated with various proteins involved in excitation-contraction coupling and mechano-electric feedback. Remodeling of the t-system has been reported for cells in culture and various types of heart disease. In this paper, we provide insights into effects of mechanical strain on the t-system in rabbit left ventricular myocytes. Based on fluorescent labeling, three-dimensional scanning confocal microscopy, and digital image analysis, we studied living and fixed isolated cells in different strain conditions. We extracted geometric features of transverse tubules (t-tubules) and characterized their arrangement with respect to the Z-disk. In addition, we studied the t-system in cells from hearts fixed either at zero left ventricular pressure (slack), at 30 mmHg (volume overload), or during lithium-induced contracture, using transmission electron microscopy. Two-dimensional image analysis was used to extract features of t-tubule cross-sections. Our analyses of confocal microscopic images showed that contracture at the cellular level causes deformation of the t-system, increasing the length and volume of t-tubules, and altering their cross-sectional shape. TEM data reconfirmed the presence of mechanically induced changes in t-tubular cross sections. In summary, our studies suggest that passive longitudinal stretching and active contraction of ventricular cardiomyocytes affect the geometry of t-tubules. This confirms that mechanical changes at cellular levels could promote alterations in partial volumes that would support a convection-assisted mode of exchange between the t-system content and extracellular space.

Indexed as

Mechanical PhenomenaActininAnimalsBiomechanical PhenomenaCell SurvivalCytoskeletonHeart VentriclesMyocytes, CardiacRabbitsSarcomeresStress, MechanicalActinin

Identifiers

PMID22884710
PMCPMC3484213
OpenAlexW2031747278

What OpenQuestion holds

Textmetadata
LicenceTDM
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.