Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10883545 | Progress in Biophysics and Molecular Biology | 2016 | 9 Pages |
Abstract
Electron tomography is particularly advantageous for studying highly compartmentalised cells such as cardiomyocytes, where elaborate sub-cellular structures play crucial roles in electrophysiology and mechanics. Although the anatomy of specific ultra-structures, such as dyadic couplons, has been extensively explored using 2D electron microscopy of thin sections, we still lack accurate, quantitative knowledge of true individual shape, volume and surface area of sub-cellular domains, as well as their 3D spatial interrelations; let alone of how these are reshaped during the cycle of contraction and relaxation. Here we discuss and illustrate the utility of ET for identification, visualisation, and analysis of 3D cardiomyocyte ultrastructures such as the T-tubular system, sarcoplasmic reticulum, mitochondria and microtubules.
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Authors
Eva A. Rog-Zielinska, Callum M. Johnston, Eileen T. O'Toole, Mary Morphew, Andreas Hoenger, Peter Kohl,