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Biophys J, December 2002, p. 3134-3151, Vol. 83, No. 6

*Department of Physiology, University of Bern, Bern, Switzerland;
and
Department of Biophysics, Bulgarian Academy of
Science, Sofia, Bulgaria
Ca2+ signaling in cells is largely governed
by Ca2+ diffusion and Ca2+ binding to mobile
and stationary Ca2+ buffers, including organelles. To
examine Ca2+ signaling in cardiac atrial myocytes, a
mathematical model of Ca2+ diffusion was developed which
represents several subcellular compartments, including a subsarcolemmal
space with restricted diffusion, a myofilament space, and the cytosol.
The model was used to quantitatively simulate experimental
Ca2+ signals in terms of amplitude, time course, and
spatial features. For experimental reference data, L-type
Ca2+ currents were recorded from atrial cells with the
whole-cell voltage-clamp technique. Ca2+ signals were
simultaneously imaged with the fluorescent Ca2+ indicator
Fluo-3 and a laser-scanning confocal microscope. The simulations
indicate that in atrial myocytes lacking T-tubules, Ca2+
movement from the cell membrane to the center of the cells relies strongly on the presence of mobile Ca2+ buffers,
particularly when the sarcoplasmic reticulum is inhibited pharmacologically. Furthermore, during the influx of Ca2+
large and steep concentration gradients are predicted between the
cytosol and the submicroscopically narrow subsarcolemmal space. In
addition, the computations revealed that, despite its low
Ca2+ affinity, ATP acts as a significant buffer and carrier
for Ca2+, even at the modest elevations of
[Ca2+]i reached during influx of
Ca2+.
Biophys J, December 2002, p. 3134-3151, Vol. 83, No. 6
© 2002 by the Biophysical Society 0006-3495/02/12/3134/18 $2.00
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