Abstract

In pancreatic acinar cells hormonal stimulation leads to a cytosolic Ca(2+) wave that starts in the apical cell pole and subsequently propagates toward the basal cell side. We used permeabilized pancreatic acinar cells from mouse and the mag-fura-2 technique, which allows direct monitoring of changes in [Ca(2+)] of intracellular stores. We show here that Ca(2+) can be released from stores in all cellular regions by inositol 1,4,5-trisphosphate. Stores at the apical cell pole showed a higher affinity to inositol 1,4,5-trisphosphate (EC(50) = 89 nm) than those at the basolateral side (EC(50) = 256 nm). In contrast, cADP-ribose, a modifier of Ca(2+)-induced Ca(2+) release, and nicotinic acid adenine dinucleotide phosphate (NAADP) were able to release Ca(2+) exclusively from intracellular stores located at the basolateral cell side. Our data agree with observations that upon stimulation Ca(2+) is released initially at the apical cell side and that this is caused by high affinity inositol 1,4,5-trisphosphate receptors. Moreover, our findings allow the conclusion that in Ca(2+) wave propagation from the apical to the basolateral cell side observed in pancreatic acinar cells Ca(2+)-induced Ca(2+) release, modulated by cADP-ribose and/or NAADP, might be involved.

Highlights

  • The mechanism underlying generation and propagation of the Ca2ϩ wave is still a matter of debate

  • To estimate [Ca2ϩ]store not influenced by the cytoplasmic dye and to test the effects of IP3, cADP-ribose, and nicotinic acid adenine dinucleotide phosphate (NAADP) on these stores, cells had to be permeabilized with streptolysin O before each experiment as described in “Experimental Procedures.”

  • In pancreatic acinar cells an increase in [Ca2ϩ]i in the apical cell pole is necessary for fusion of zymogen granules with the apical plasma membrane and for opening of ClϪ channels, which leads to exocytosis of proteins and secretion of ClϪ, respectively

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Summary

Introduction

The mechanism underlying generation and propagation of the Ca2ϩ wave is still a matter of debate. Our findings allow the conclusion that in Ca2؉ wave propagation from the apical to the basolateral cell side observed in pancreatic acinar cells Ca2؉-induced Ca2؉ release, modulated by cADP-ribose and/or NAADP, might be involved. IP3 added to pancreatic acinar cells at low concentrations (0.1–1 ␮M) releases Ca2ϩ mainly from stores located in the apical cell pole.

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