AUTHOR=Kekenes-Huskey Peter M., Cheng Yuhui , Hake Johan E., Sachse Frank B., Bridge John H., Holst Michael J., McCammon J Andrew , McCulloch Andrew D., Michailova Anushka P. TITLE=Modeling Effects of L-Type Ca2+ Current and Na+-Ca2+ Exchanger on Ca2+ Trigger Flux in Rabbit Myocytes with Realistic T-Tubule Geometries JOURNAL=Frontiers in Physiology VOLUME=3 YEAR=2012 URL=https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2012.00351 DOI=10.3389/fphys.2012.00351 ISSN=1664-042X ABSTRACT=

The transverse tubular system of rabbit ventricular myocytes consists of cell membrane invaginations (t-tubules) that are essential for efficient cardiac excitation-contraction coupling. In this study, we investigate how t-tubule micro-anatomy, L-type Ca²⁺ channel (LCC) clustering, and allosteric activation of Na⁺/Ca²⁺ exchanger by L-type Ca²⁺ current affects intracellular Ca²⁺ dynamics. Our model includes a realistic 3D geometry of a single t-tubule and its surrounding half-sarcomeres for rabbit ventricular myocytes. The effects of spatially distributed membrane ion-transporters (LCC, Na⁺/Ca²⁺ exchanger, sarcolemmal Ca²⁺ pump, and sarcolemmal Ca²⁺ leak), and stationary and mobile Ca²⁺ buffers (troponin C, ATP, calmodulin, and Fluo-3) are also considered. We used a coupled reaction-diffusion system to describe the spatio-temporal concentration profiles of free and buffered intracellular Ca²⁺. We obtained parameters from voltage-clamp protocols of L-type Ca²⁺ current and line-scan recordings of Ca²⁺ concentration profiles in rabbit cells, in which the sarcoplasmic reticulum is disabled. Our model results agree with experimental measurements of global Ca²⁺ transient in myocytes loaded with 50 μM Fluo-3. We found that local Ca²⁺ concentrations within the cytosol and sub-sarcolemma, as well as the local trigger fluxes of Ca²⁺ crossing the cell membrane, are sensitive to details of t-tubule micro-structure and membrane Ca²⁺ flux distribution. The model additionally predicts that local Ca²⁺ trigger fluxes are at least threefold to eightfold higher than the whole-cell Ca²⁺ trigger flux. We found also that the activation of allosteric Ca²⁺-binding sites on the Na⁺/Ca²⁺ exchanger could provide a mechanism for regulating global and local Ca²⁺ trigger fluxes in vivo. Our studies indicate that improved structural and functional models could improve our understanding of the contributions of L-type and Na⁺/Ca²⁺ exchanger fluxes to intracellular Ca²⁺ dynamics.