Co-ordination of Ca2+ signalling in mammalian cells by the new Ca2+ releasing messenger NAADP

被引:28
作者
Cancela, JM
Charpentier, G
Petersen, OH
机构
[1] CNRS, Neurobiol Cellulaire & Mol Lab, UPR 9040, F-91198 Gif Sur Yvette, France
[2] Univ Picardie, Fac Sci, Physiol Anim Lab, F-80018 Amiens, France
[3] Univ Liverpool, Physiol Lab, MRC, Secretory Control Res Grp, Liverpool L69 3BX, Merseyside, England
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2003年 / 446卷 / 03期
关键词
NAADP; cyclic ADP-ribose; inositol trisphosphate; calcium; thapsigargin; CD38; ADP-ribosyl cyclase;
D O I
10.1007/s00424-003-1035-x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Ca2+ signalling is one of the most important means in mammalian cells of relaying the action of hormones and neurotransmitters. The great diversity of agonist-induced Ca2+ signatures, visualized by optical imaging techniques, can be explained by the production of intracellular messengers triggering Ca2+ release from internal stores and/or by different coupling of Ca2+ release to Ca2+ entry. Several messengers, such as inositol trisphosphate and cyclic ADP-ribose, have been identified to date. More recent studies have reported the important role of a newly discovered Ca2+ releasing messenger, nicotinic acid adenine dinucleotide phosphate (NAADP). These studies have shown important interactions of these messengers in the generation of specific Ca2+ signals. NAADP acts at a very low concentration and seems to have a key role in sensitising cyclic ADP-ribose and inositol trisphosphate receptors. These points will be discussed in the present review.
引用
收藏
页码:322 / 327
页数:6
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