Diffusional and Electrical Properties of T-Tubules Are Governed by Their Constrictions and Dilations

• Published in: Biophysical journal 2018-01, Vol.114 (2), p.437-449
• Main Authors: Uchida, Keita, Lopatin, Anatoli N.
• Format: Article
• Language: English
• Subjects: Accessibility; Bioassays; Cardiac muscle; Cell Biophysics; Cell size; Cells; Constrictions; Contraction; Cylinders; Dextran; Diffusion; Diffusion rate; Electrical properties; Excitation-contraction coupling; Fluorescence; Heart; Heart diseases; Invaginations; Measurement; Microscopy; Myocytes; Optical microscopy; Time constant; Tubules; Ventricle
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/j.bpj.2017.11.3742

Cardiac t-tubules (TTs) form a network of complex surface membrane invaginations that is essential for proper excitation-contraction coupling. Although electron and optical microscopy studies provided a wealth of important information about the structure of TTs, assessing their functional properties remains a challenge. In this study, we investigated the diffusional accessibility of TTs in intact isolated adult mouse ventricular myocytes using, to our knowledge, a novel fluorescence-based assay. In this approach, a small part of TTs is first locally filled with fluorescent dextran and then its diffusion out of TTs is monitored after rapid removal of extracellular dextran. In normal cells, diffusion of 3 kDa dextran is characterized by an average time constant of 3.9 ± 1.2 s with the data ranging from 1.8 to 10.5 s. The data are consistent with essentially free diffusion of dextran in TTs although measurable contribution of binding is also evident. TT fluorescence is abolished in cells treated with high concentration of formamide or after hyposmotic stress. Importantly, the assay we use allows for quantitative, repetitive measurements of subtle dynamic changes in TT structure of the same cell that are not possible to observe with other approaches. In particular, dextran diffusion rate decreases two-to-threefold during cell swelling, suggesting significant structural remodeling of TTs. Computer modeling shows that diffusional accessibility and electrical properties of TTs are primarily determined by the constrictions and dilations of individual TTs and that, from a functional perspective, TTs cannot be considered as a network of cylinders of the same average diameter. Constriction/dilation model of cardiac TTs is in a quantitative agreement with previous high-resolution microscopy studies of TT structure and alternative measurements of diffusional and electrical time constants of TTs. The data also show that the apparent electrical length constant of cardiac TTs is likely several-fold smaller than that estimated in earlier studies.