The localizations of Ca2+ extrusion sites in mouse pancreatic acinar c
ells during elevation of the intracellular free calcium concentration
([Ca2+](i)) have been studied. During an agonist stimulated calcium el
evation as well as when intracellular calcium is released from a 'cage
d compound', Ca2+ is primarily extruded from the apical secretory pole
of the cells in spite of different spatial patterns of [Ca2+](i), dif
ferent sources of Ca2+, and the presence or absence of agonist, This i
s most likely due to a relatively high density of calcium pumps in the
secretory granule region, although it could be explained by calcium p
umps in this part of the cell having different characteristics from th
ose in the basal membrane. The intensity of Ca2+ extrusion in the apic
al secretory pole is such that substantial (several millimoles per lit
re) changes of the free calcium concentration in the lumen of the acin
us can occur during agonist stimulation.