Multiplicity of Ca2+ messengers and Ca2+ stores:: A perspective from cyclic ADP-ribose and NAADP

被引:109
作者
Lee, HC [1 ]
机构
[1] Univ Minnesota, Dept Pharmacol, Minneapolis, MN 55455 USA
关键词
cyclic ADP-Ribose (cADPR); NAADP; ADP-ribosyl cyclase; CD38; mobilization of Ca2+ stores; Ca2+ signaling;
D O I
10.2174/1566524043360753
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
It is generally believed that multiple Ca2+ stores are present in cells, a notion that has now been made substantive by the discovery of multiple Ca2+ mobilizing messengers. Cyclic ADP-ribose (cADPR) and nicotinic acid dinucleotide phosphate (NAADP) are two such messengers that are derived from NAD and NADP, respectively. A wide variety of cells, from plants to mammals, including human, have been shown to be responsive to these two novel Ca2+ messengers. Not only are their structures and mechanisms of action different, their targeted Ca2+ stores are also distinct and separable. This article explores the implications of the multiplicity of Ca2+ stores in cellular signaling. Special emphasis will be put on the recent progress in the understanding of the physiological functions of NAADP.
引用
收藏
页码:227 / 237
页数:11
相关论文
共 123 条
[31]   Inhibition of cADP-ribose formation produces vasodilation in bovine coronary arteries [J].
Geiger, J ;
Zou, AP ;
Campbell, WB ;
Li, PL .
HYPERTENSION, 2000, 35 (01) :397-402
[32]   Pharmacological properties of the Ca2+-release mechanism sensitive to NAADP in the sea urchin egg [J].
Genazzani, AA ;
Mezna, M ;
Dickey, DM ;
Michelangeli, F ;
Walseth, TF ;
Galione, A .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (07) :1489-1495
[33]   Nicotinic acid-adenine dinucleotide phosphate mobilizes Ca2+ from a thapsigargin-insensitive pool [J].
Genazzani, AA ;
Galione, A .
BIOCHEMICAL JOURNAL, 1996, 315 :721-725
[34]   Unique inactivation properties of NAADP-sensitive Ca2+ release [J].
Genazzani, AA ;
Empson, RM ;
Galione, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (20) :11599-11602
[35]   ATP-DEPENDENT ACCUMULATION AND INOSITOL TRISPHOSPHATE-MEDIATED OR CYCLIC ADP-RIBOSE-MEDIATED RELEASE OF CA2+ FROM THE NUCLEAR-ENVELOPE [J].
GERASIMENKO, OV ;
GERASIMENKO, JV ;
TEPIKIN, AV ;
PETERSEN, OH .
CELL, 1995, 80 (03) :439-444
[36]   A novel cycling assay for cellular cADP-ribose with nanomolar sensitivity [J].
Graeff, R ;
Lee, HC .
BIOCHEMICAL JOURNAL, 2002, 361 (02) :379-384
[37]   A novel cycling assay for nicotinic acid-adenine dinucleotide phosphate with nanomolar sensitivity [J].
Graeff, R ;
Lee, HC .
BIOCHEMICAL JOURNAL, 2002, 367 (01) :163-168
[38]   A single residue at the active site of CD38 determines its NAD cyclizing and hydrolyzing activities [J].
Graeff, R ;
Munshi, C ;
Aarhus, R ;
Johns, M ;
Lee, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (15) :12169-12173
[39]   Cyclic GMP-dependent and -independent effects on the synthesis of the calcium messengers cyclic ADP-ribose and nicotinic acid adenine dinucleotide phosphate [J].
Graeff, RM ;
Franco, L ;
De Flora, A ;
Lee, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :118-125
[40]   Equilibrative and concentrative nucleoside transporters mediate influx of extracellular cyclic ADP-ribose into 3T3 murine fibroblasts [J].
Guida, L ;
Bruzzone, S ;
Sturla, L ;
Franco, L ;
Zocchi, E ;
De Flora, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :47097-47105