Evidence map›Paper›PMID 28507142›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Quantitative assessment of passive electrical properties of the cardiac T-tubular system by FRAP microscopy.

M Scardigli, C Crocini, C Ferrantini, T Gabbrielli, L Silvestri, R Coppini, C Tesi, E A Rog-Zielinska, P Kohl, E Cerbai and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. T-tubule remodeling in human hypertrophic cardiomyopathy.Journal of muscle research and cell motility · 2021
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Species differences in the morphology of transverse tubule openings in cardiomyocytes.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2018
    Article
  14. Article
  15. Solute movement in the t-tubule system of rabbit and mouse cardiomyocytes.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Uncovering an electrically heterogeneous cardiomyocyte by FRAP-quantified diffusion in the T-tubules.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Reply to Entcheva: The impact of T-tubules on action potential propagation in cardiac tissue.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
  19. Axial Tubule Junctions Activate Atrial CaFrontiers in physiology · 2018
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 3 countries.

M ScardigliEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.
C CrociniEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.ORCID 0000-0001-8231-2726
C FerrantiniDivision of Physiology, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, Italy.
T GabbrielliEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.
L SilvestriEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.
R CoppiniDivision of Pharmacology, Dipartimento di Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino, University of Florence, 50139 Florence, Italy.
C TesiDivision of Physiology, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, Italy.
E A Rog-ZielinskaInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg-Bad Krozingen, Faculty of Medicine, University of Freiburg, 79110 Freiburg, Germany.
P KohlInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg-Bad Krozingen, Faculty of Medicine, University of Freiburg, 79110 Freiburg, Germany.
E CerbaiDivision of Pharmacology, Dipartimento di Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino, University of Florence, 50139 Florence, Italy.
C PoggesiDivision of Physiology, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, Italy.
F S PavoneEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.
L SacconiEuropean Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy; sacconi@lens.unifi.it.
National Research Council · ITUniversity of Florence · ITUniversity of Freiburg · DE

Funding

British Heart Foundation FS/12/17/29532British Heart Foundation FS/15/3/31047
6 · The paper itself

Abstract

Well-coordinated activation of all cardiomyocytes must occur on every heartbeat. At the cell level, a complex network of sarcolemmal invaginations, called the transverse-axial tubular system (TATS), propagates membrane potential changes to the cell core, ensuring synchronous and uniform excitation-contraction coupling. Although myocardial conduction of excitation has been widely described, the electrical properties of the TATS remain mostly unknown. Here, we exploit the formal analogy between diffusion and electrical conductivity to link the latter with the diffusional properties of TATS. Fluorescence recovery after photobleaching (FRAP) microscopy is used to probe the diffusion properties of TATS in isolated rat cardiomyocytes: A fluorescent dextran inside TATS lumen is photobleached, and signal recovery by diffusion of unbleached dextran from the extracellular space is monitored. We designed a mathematical model to correlate the time constant of fluorescence recovery with the apparent diffusion coefficient of the fluorescent molecules. Then, apparent diffusion is linked to electrical conductivity and used to evaluate the efficiency of the passive spread of membrane depolarization along TATS. The method is first validated in cells where most TATS elements are acutely detached by osmotic shock and then applied to probe TATS electrical conductivity in failing heart cells. We find that acute and pathological tubular remodeling significantly affect TATS electrical conductivity. This may explain the occurrence of defects in action potential propagation at the level of single T-tubules, recently observed in diseased cardiomyocytes.

Indexed as

Action PotentialsAnimalsCalcium SignalingCells, CulturedCell Surface ExtensionsExcitation Contraction CouplingFluorescence Recovery After PhotobleachingHeart Conduction SystemMaleModels, TheoreticalMyocardiumMyocytes, CardiacRatsRats, Inbred WKYSarcolemmaSarcoplasmic Reticulumcardiac diseasediffusionelectrical conductivityporous rocktransverse-axial tubular system

Identifiers

PMID28507142
PMCPMC5465880
OpenAlexW2615372385

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.