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Biophys J, January 2000, p. 13-33, Vol. 78, No. 1
Instituto de Bioingeniería, Universidad Miguel Hernández, 03202 Elche, Alicante, Spain
Buffered Ca2+ diffusion in the cytosol of
neuroendocrine cells is a plausible explanation for the slowness and
latency in the secretion of hormones. We have developed a Monte Carlo
simulation to treat the problem of 3-D diffusion and kinetic reactions
of ions and buffers. The 3-D diffusion is modeled as a random walk process that follows the path of each ion and buffer molecule, combined
locally with a stochastic treatment of the first-order kinetic
reactions involved. Such modeling is able to predict
[Ca2+] and buffer concentration time courses regardless
of how low the calcium influx is, and it is therefore a convenient
method for dealing with physiological calcium currents and
concentrations. We study the effects of the diffusional and kinetic
parameters of the model on the concentration time courses as well as on
the local equilibrium of buffers with calcium. An in-mobile and fast endogenous buffer as described by Klingauf and Neher (1997,
Biophys. J. 72:674-690) was able to reach local equilibrium
with calcium; however, the exogenous buffers considered are displaced
drastically from equilibrium at the start of the calcium pulse,
particularly below the pores. The versatility of the method also allows
the effect of different arrangements of calcium channels on submembrane gradients to be studied, including random distribution of calcium channels and channel clusters. The simulation shows how the particular distribution of channels or clusters can be of relevance for secretion in the case where the distribution of release granules is correlated with the channels or clusters.
Biophys J, January 2000, p. 13-33, Vol. 78, No. 1
© 2000 by the Biophysical Society 0006-3495/00/01/13/21 $2.00
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