We present a theoretical investigation of the effect of Ca2+ influx th
rough ion channels in the plasma membrane on Ca2+ oscillations induced
by agonist stimulation of Ca2+ release from internal stores. We expan
d a recent model of internal Ca2+ oscillations based on activation and
inhibition of the IP3-receptor in the endoplasmic reticulum by introd
ucing plasma membrane voltage-gated Ca2+ and K+ channels based on patc
h-clamp experiments on mouse pancreatic beta cells. Simulations of vol
tage- and current-clamped experiments are carried out. The amplitude a
nd frequency of the oscillations as well as the sensitivity to agonist
are strongly affected by altering the value of the voltage-clamp. We
show that the fundamental quantity governing voltage clamp measurement
s is the inward flux of Ca2+, which acts as a control parameter to alt
er characteristics of the oscillations. Under current clamp conditions
(I(applied) = 0) that lead to continuous spiking electrical activity,
we examine the couping between electrical activity and Ca2+ by introd
ucing a small whole cell Ca2+-activated K+ conductance. Results of cal
culations are similar to those observed in agonist-stimulated beta cel
ls and gonadotrophs. We conclude, however, that glucose-induced bursti
ng and agonist induced bursting in beta cells are distinct phenomena a
nd suggest a mechanism by which agonist-induced Ca2+ oscillations migh
t potentiate insulin secretion. This leads to a general principle for
selective signal transduction by Ca2+ oscillations.