A bimodal pattern of InsP(3)-evoked elementary Ca(2+) signals in pancreatic acinar cells

Biophys J. 2000 May;78(5):2298-306. doi: 10.1016/S0006-3495(00)76776-2.

Abstract

InsP(3)-evoked elementary Ca(2+) release events have been postulated to play a role in providing the building blocks of larger Ca(2+) signals. In pancreatic acinar cells, low concentrations of acetylcholine or the injection of low concentrations of InsP(3) elicit a train of spatially localized Ca(2+) spikes. In this study we have quantified these responses and compared the Ca(2+) signals to the elementary events shown in Xenopus oocytes. The results demonstrate, at the same concentrations of InsP(3), Ca(2+) signals consisting of one population of small transient Ca(2+) release events and a second distinct population of larger Ca(2+) spikes. The signal mass amplitudes of both types of events are within the range of amplitudes for the elementary events in Xenopus oocytes. However, the bimodal Ca(2+) distribution of Ca(2+) responses we observe is not consistent with the continuum of event sizes seen in Xenopus. We conclude that the two types of InsP(3)-dependent events in acinar cells are both elementary Ca(2+) signals, which are independent of one another. Our data indicate a complexity to the organization of the Ca(2+) release apparatus in acinar cells, which might result from the presence of multiple InsP(3) receptor isoforms, and is likely to be important in the physiology of these cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biophysical Phenomena
  • Biophysics
  • Calcium Channels / metabolism
  • Calcium Signaling / drug effects*
  • Female
  • In Vitro Techniques
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Inositol 1,4,5-Trisphosphate / pharmacology*
  • Inositol 1,4,5-Trisphosphate Receptors
  • Male
  • Mice
  • Microscopy, Fluorescence
  • Oocytes / metabolism
  • Pancreas / cytology
  • Pancreas / drug effects*
  • Pancreas / metabolism*
  • Patch-Clamp Techniques
  • Protein Isoforms / metabolism
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Xenopus

Substances

  • Calcium Channels
  • Inositol 1,4,5-Trisphosphate Receptors
  • Protein Isoforms
  • Receptors, Cytoplasmic and Nuclear
  • Inositol 1,4,5-Trisphosphate