Transformation of local Ca2+ spikes to global Ca2+ transients: the combinatorial roles of multiple Ca2+ releasing messengers

EMBO J. 2002 Mar 1;21(5):909-19. doi: 10.1093/emboj/21.5.909.

Abstract

In pancreatic acinar cells, low, threshold concentrations of acetylcholine (ACh) or cholecystokinin (CCK) induce repetitive local cytosolic Ca2+ spikes in the apical pole, while higher concentrations elicit global signals. We have investigated the process that transforms local Ca2+ spikes to global Ca2+ transients, focusing on the interactions of multiple intracellular messengers. ACh-elicited local Ca2+ spikes were transformed into a global sustained Ca2+ response by cyclic ADP-ribose (cADPR) or nicotinic acid adenine dinucleotide phosphate (NAADP), whereas inositol 1,4,5-trisphosphate (IP3) had a much weaker effect. In contrast, the response elicited by a low CCK concentration was strongly potentiated by IP3, whereas cADPR and NAADP had little effect. Experiments with messenger mixtures revealed a local interaction between IP3 and NAADP and a stronger global potentiating interaction between cADPR and NAADP. NAADP strongly amplified the local Ca2+ release evoked by a cADPR/IP3 mixture eliciting a vigorous global Ca2+ response. Different combinations of Ca2+ releasing messengers can shape the spatio-temporal patterns of cytosolic Ca2+ signals. NAADP and cADPR are emerging as key messengers in the globalization of Ca2+ signals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Adenosine Diphosphate Ribose / analogs & derivatives*
  • Adenosine Diphosphate Ribose / physiology*
  • Animals
  • Caffeine / pharmacology
  • Calcium Channels / drug effects
  • Calcium Channels / physiology
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology*
  • Cell Polarity
  • Cholecystokinin / pharmacology
  • Cyclic ADP-Ribose
  • Exocytosis / drug effects
  • Inositol 1,4,5-Trisphosphate / pharmacology
  • Inositol 1,4,5-Trisphosphate / physiology*
  • Inositol 1,4,5-Trisphosphate Receptors
  • Mice
  • NADP / analogs & derivatives*
  • NADP / pharmacology
  • NADP / physiology*
  • Pancreas / cytology
  • Patch-Clamp Techniques
  • Receptors, Cell Surface / drug effects
  • Receptors, Cell Surface / physiology
  • Receptors, Cholecystokinin / drug effects
  • Receptors, Cholecystokinin / physiology
  • Receptors, Cholinergic / drug effects
  • Receptors, Cholinergic / physiology
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Second Messenger Systems / physiology*
  • Sincalide / pharmacology

Substances

  • Calcium Channels
  • Inositol 1,4,5-Trisphosphate Receptors
  • Receptors, Cell Surface
  • Receptors, Cholecystokinin
  • Receptors, Cholinergic
  • Receptors, Cytoplasmic and Nuclear
  • cyclic ADP-ribose receptor
  • Cyclic ADP-Ribose
  • Adenosine Diphosphate Ribose
  • Caffeine
  • NADP
  • NAADP
  • Inositol 1,4,5-Trisphosphate
  • Cholecystokinin
  • Sincalide
  • Acetylcholine