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

被引:146
作者
Cancela, JM
Van Coppenolle, F
Galione, A
Tepikin, AV
Petersen, OH
机构
[1] Neurobiol Cellulaire & Mol Lab, CNRS, UPR 9040, F-91198 Gif Sur Yvette, France
[2] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[3] Univ Liverpool, Physiol Lab, MRC, Secretory Control Res Grp, Liverpool L69 3BX, Merseyside, England
关键词
cyclic ADP-ribose; inositol trisphosphate; local and global calcium; NAADP; pancreatic acinar cells;
D O I
10.1093/emboj/21.5.909
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Call signals.
引用
收藏
页码:909 / 919
页数:11
相关论文
共 75 条
[1]   Calcium signaling by cyclic ADP-ribose, NAADP, and inositol trisphosphate are involved in distinct functions in ascidian oocytes [J].
Albrieux, M ;
Lee, HC ;
Villaz, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14566-14574
[2]   Nicotinic acid adenine dinucleotide phosphate (NAADP+) is an essential regulator of T-lymphocyte Ca2+-signaling [J].
Berg, I ;
Potter, BVL ;
Mayr, GW ;
Guse, AH .
JOURNAL OF CELL BIOLOGY, 2000, 150 (03) :581-588
[3]   The versatility and universality of calcium signalling [J].
Berridge, MJ ;
Lipp, P ;
Bootman, MD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) :11-21
[4]   Calcium - a life and death signal [J].
Berridge, MJ ;
Bootman, MD ;
Lipp, P .
NATURE, 1998, 395 (6703) :645-648
[5]   Elementary and global aspects of calcium signalling [J].
Berridge, MJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 499 (02) :291-306
[6]   Inositol 1,4,5-trisphosphate- and ryanodine-sensitive Ca2+ release channel dependent Ca2+ signalling in rat portal vein myocytes [J].
Boittin, FX ;
Coussin, F ;
Macrez, N ;
Mironneau, C ;
Mironneau, J .
CELL CALCIUM, 1998, 23 (05) :303-311
[7]   THE OPENING OF THE INOSITOL 1,4,5-TRISPHOSPHATE-SENSITIVE CA2+ CHANNEL IN RAT CEREBELLUM IS INHIBITED BY CAFFEINE [J].
BROWN, GR ;
SAYERS, LG ;
KIRK, CJ ;
MICHELL, RH ;
MICHELANGELI, F .
BIOCHEMICAL JOURNAL, 1992, 282 :309-312
[8]   Intracellular glucose switches between cyclic ADP-ribose and inositol trisphosphate triggering of cytosolic Ca2+ spiking [J].
Cancela, JM ;
Mogami, H ;
Tepikin, AV ;
Petersen, OH .
CURRENT BIOLOGY, 1998, 8 (15) :865-868
[9]   Specific Ca2+ signaling evoked by cholecystokinin and acetylcholine:: The roles of NAADP, cADPR, and IP3 [J].
Cancela, JM .
ANNUAL REVIEW OF PHYSIOLOGY, 2001, 63 :99-117
[10]   Coordination of agonist-induced Ca2+-signalling patterns by NAADP in pancreatic acinar cells [J].
Cancela, JM ;
Churchill, GC ;
Galione, A .
NATURE, 1999, 398 (6722) :74-76