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Biophys J, May 2000, p. 2222-2240, Vol. 78, No. 5
and
*The Neurobiology Laboratory, Institute for Biomedical Research,
Department of Physiology, and
The School of Mathematics
and Statistics, University of Sydney, New South Wales 2006, Australia
A Monte Carlo analysis has been made of calcium dynamics
in submembranous domains of active zones in which the calcium
contributed by the opening of many channels is pooled. The kinetics of
calcium ions in these domains has been determined using simulations for channels arranged in different geometries, according to the active zone
under consideration: rectangular grids for varicosities and boutons and
lines for motor-nerve terminals. The effects of endogenous fixed and
mobile buffers on the two-dimensional distribution of free calcium ions
at these active zones are then given, together with the extent to which
these are perturbed and can be detected with different affinity calcium
indicators when the calcium channels open stochastically under an
action potential. A Monte Carlo analysis of how the dynamics of calcium
ions in the submembranous domains determines the probability of
exocytosis from docked vesicles is also presented. The spatial
distribution of exocytosis from rectangular arrays of secretory units
is such that exocytosis is largely excluded from the edges of the
array, due to the effects of endogenous buffers. There is a steeper
than linear increase in quantal release with an increase in the number
of secretory units in the array, indicating that there is not just a
local interaction between secretory units. Conditioning action
potentials promote an increase in quantal release by a subsequent
action potential primarily by depleting the fixed and mobile buffers in
the center of the array. In the case of two parallel lines of secretory
units exocytosis is random, and diffusion, together with the endogenous
calcium buffers, ensures that the secretory units only interact over
relatively short distances. As a consequence of this and in contrast to
the case of the rectangular array, there is a linear relationship
between the extent of quantal secretion from these zones and their
length, for lengths greater than a critical value. This Monte Carlo
analysis successfully predicts the relationship between the size and
geometry of active zones and the probability of quantal secretion at
these, the existence of quantal versus multiquantal release at
different active zones, and the origins of the F1 phase of facilitation
in synapses possessing different active zone geometries.
Biophys J, May 2000, p. 2222-2240, Vol. 78, No. 5
© 2000 by the Biophysical Society 0006-3495/00/05/2222/19 $2.00
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