Integration of nicotinic acid adenine dinucleotide phosphate (NAADP)-dependent calcium signalling

被引:27
|
作者
Guse, Andreas H. [1 ]
Diercks, Bjoern-Philipp [1 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Biochem & Mol Cell Biol, Calcium Signalling Grp, Martinistr 52, D-20246 Hamburg, Germany
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2018年 / 596卷 / 14期
基金
英国惠康基金;
关键词
calcium signaling; NAADP; calcium release; NAADP MOBILIZES CALCIUM; CYCLIC ADP-RIBOSE; RYANODINE RECEPTOR; CA2+ MICRODOMAINS; ENDOPLASMIC-RETICULUM; 2-PORE CHANNELS; ORGANELLES; RELEASE; CD38; ER;
D O I
10.1113/JP275974
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nicotinic acid adenine dinucleotide phosphate (NAADP) is currently the most potent endogenous Ca2+ mobilizing second messenger. Upon specific extracellular stimulation, rapid production of NAADP has been observed in different cell types from sea urchin eggs to mammalian cells. More than 20years after the discovery of NAADP, there is still controversy surrounding its metabolism and target receptors/ion channels and organelles. This article briefly reviews recent developments in the NAADP field. Besides the metabolism of NAADP, this review focuses on assumed organelles and putative targets, e.g. ion channels, with special emphasis on ryanodine receptor type 1 (RyR1) and two-pore channels (TPCs). The role of NAADP as a Ca2+ trigger is also discussed and the importance of NAADP in the formation of initial Ca2+ microdomains is highlighted.
引用
收藏
页码:2735 / 2743
页数:9
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