Evidence map›Paper›PMID 25160725›Full record

ArticleJournal of structural biology2014

Nanoscale three-dimensional imaging of the human myocyte.

Matthew S Sulkin, Fei Yang, Katherine M Holzem, Brandon Van Leer, Cliff Bugge, Jacob I Laughner, Karen Green, Igor R Efimov

Abstract read
In one paragraph

Article in Journal of structural biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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
  7. Article
  8. Article
  9. Review
  10. Electron tomography of rabbit cardiomyocyte three-dimensional ultrastructure.Progress in biophysics and molecular biology · 2016
    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

8 authors.

Matthew S SulkinDepartment of Biomedical Engineering, Washington University in St. Louis, MO, USA.
Fei YangDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, MO, USA.
Katherine M HolzemDepartment of Biomedical Engineering, Washington University in St. Louis, MO, USA.
Brandon Van LeerFEI Company, Hillsboro, OR, USA.
Cliff BuggeFEI Company, Hillsboro, OR, USA.
Jacob I LaughnerDepartment of Biomedical Engineering, Washington University in St. Louis, MO, USA.
Karen GreenDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, MO, USA.
Igor R EfimovDepartment of Biomedical Engineering, Washington University in St. Louis, MO, USA. Electronic address: igor@wustl.edu.

Funding

ARRHYTHMOGENIC REMODELING IN HUMAN HEART FAILURER01HL114395 · NHLBI · WASHINGTON UNIVERSITY · PI EFIMOV, IGOR R · 2012 to 2015
$2.1M
Arrhythmogenic Remodeling of Repolarization in Human Heart FailureF30HL114310 · NHLBI · WASHINGTON UNIVERSITY · PI HOLZEM, KATHERINE MARIE · 2013 to 2016
$174k
NHLBI NIH HHS F30 HL114310NHLBI NIH HHS R01 HL114395
6 · The paper itself

Abstract

The ventricular human myocyte is spatially organized for optimal ATP and Ca(2+) delivery to sarcomeric myosin and ionic pumps during every excitation-contraction cycle. Comprehension of three-dimensional geometry of the tightly packed ultrastructure has been derived from discontinuous two-dimensional images, but has never been precisely reconstructed or analyzed in human myocardium. Using a focused ion beam scanning electron microscope, we created nanoscale resolution serial images to quantify the three-dimensional ultrastructure of a human left ventricular myocyte. Transverse tubules (t-tubule), lipid droplets, A-bands, and mitochondria occupy 1.8, 1.9, 10.8, and 27.9% of the myocyte volume, respectively. The complex t-tubule system has a small tortuosity (1.04±0.01), and is composed of long transverse segments with diameters of 317±24nm and short branches. Our data indicates that lipid droplets located well beneath the sarcolemma are proximal to t-tubules, where 59% (13 of 22) of lipid droplet centroids are within 0.50μm of a t-tubule. This spatial association could have an important implication in the development and treatment of heart failure because it connects two independently known pathophysiological alterations, a substrate switch from fatty acids to glucose and t-tubular derangement.

Indexed as

Adenosine TriphosphateCalciumHeart VentriclesHumansImaging, Three-DimensionalLipid DropletsMicroscopy, Electron, ScanningMuscle CellsMyocardiumMyocytes, CardiacSarcolemmaAdenosine TriphosphateCalciumFocused ion beam tomographyMetabolismMyocyteUltrastructure

Identifiers

PMID25160725
PMCPMC4295200

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.