The role of Ca2+ in initiating exocytosis of granule-bound secretory p
roducts was evaluated with respect to pancreatic islet hormones. Apart
from stimulating the transfer of the granules to the plasma membrane
and their subsequent extrusion, a rise of the cytoplasmic Ca2+ concent
ration ([Ca2+](i)) may under certain conditions also have depressive e
ffects on insulin release. Glucose has a bidirectional action on [Ca2](i) by stimulating both the entry of the ion and its removal by organ
elle sequestration and outward transport. The recognition of glucose a
s a secretory stimulus is based on sudden transitions between oscillat
ory and steady-state [Ca2+](i) at threshold concentrations of the suga
r characteristic for the individual beta-cell. The intrinsic ability o
f each beta-cell to generate oscillations of [Ca2+](i) and the subsequ
ent synchronization of these signals result in a pulsatile release of
insulin from isolated islets. Glucose regulation of this process is ma
nifested as alterations of the amplitudes of the insulin pulses withou
t effects on the frequency. It is suggested that electrical signalling
from the beta-cells in combination with direct effects of glucose are
important for regulating the release of glucagon and somatostatin.