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
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylcholine / pharmacology
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Adenosine Diphosphate Ribose / analogs & derivatives*
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Adenosine Diphosphate Ribose / physiology*
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Animals
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Caffeine / pharmacology
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Calcium Channels / drug effects
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Calcium Channels / physiology
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Calcium Signaling / drug effects
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Calcium Signaling / physiology*
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Cell Polarity
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Cholecystokinin / pharmacology
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Cyclic ADP-Ribose
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Exocytosis / drug effects
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Inositol 1,4,5-Trisphosphate / pharmacology
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Inositol 1,4,5-Trisphosphate / physiology*
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Inositol 1,4,5-Trisphosphate Receptors
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Mice
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NADP / analogs & derivatives*
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NADP / pharmacology
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NADP / physiology*
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Pancreas / cytology
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Patch-Clamp Techniques
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Receptors, Cell Surface / drug effects
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Receptors, Cell Surface / physiology
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Receptors, Cholecystokinin / drug effects
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Receptors, Cholecystokinin / physiology
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Receptors, Cholinergic / drug effects
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Receptors, Cholinergic / physiology
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Receptors, Cytoplasmic and Nuclear / drug effects
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Receptors, Cytoplasmic and Nuclear / physiology
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Second Messenger Systems / physiology*
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Sincalide / pharmacology
Substances
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Calcium Channels
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Inositol 1,4,5-Trisphosphate Receptors
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Receptors, Cell Surface
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Receptors, Cholecystokinin
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Receptors, Cholinergic
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Receptors, Cytoplasmic and Nuclear
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cyclic ADP-ribose receptor
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Cyclic ADP-Ribose
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Adenosine Diphosphate Ribose
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Caffeine
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NADP
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NAADP
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Inositol 1,4,5-Trisphosphate
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Cholecystokinin
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Sincalide
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Acetylcholine