CD38 is the major enzyme responsible for synthesis of nicotinic acid-adenine dinucleotide phosphate in mammalian tissues

被引:76
作者
Chini, EN
Chini, CCS
Kato, I
Takasawa, S
Okamoto, H
机构
[1] Mayo Clin & Mayo Fdn, Dept Anesthesia, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Immunol, Rochester, MN 55905 USA
[3] Tohoku Univ, Grad Sch Med, Dept Biochem, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
Ca2+ release; cyclic ADP-ribose; knockout mice;
D O I
10.1042/0264-6021:3620125
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 the present study, we have determined the role of the enzyme CD38 upon the synthesis of the Ca2+-releasing nucleotide nicotinic acid-adenine dinucleotide phosphate (NAADP). In rat tissues, we observed that the capacity for NAADP synthesis could be co-immunoprecipitated with CD38 using an anti-CD38 antibody. Furthermore, we observed that several tissues from CD38 knockout mice had no capacity for the synthesis of this nucleotide. In addition, CD38 was also identified as the major enzyme responsible for the synthesis of the second messenger cyclic ADP-ribose. These observations lead to the conclusion that CD38 is the major enzyme responsible for the synthesis of NAADP and cyclic ADP-ribose, and raises the possibility of a new signalling pathway where two different Call-releasing nucleotides are synthesized by the same enzyme.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 34 条
[1]   ADP-ribosyl cyclase and CD38 catalyze the synthesis of a calcium-mobilizing metabolite from NADP(+) [J].
Aarhus, R ;
Graeff, RM ;
Dickey, DM ;
Walseth, TF ;
Lee, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (51) :30327-30333
[2]   Nicotinic acid adenine dinucleotide phosphate triggers Ca2+ release from brain microsomes [J].
Bak, J ;
White, P ;
Timár, G ;
Missiaen, L ;
Genazzani, AA ;
Galione, A .
CURRENT BIOLOGY, 1999, 9 (14) :751-754
[3]   CELL SIGNALING - A TALE OF 2 MESSENGERS [J].
BERRIDGE, MJ .
NATURE, 1993, 365 (6445) :388-389
[4]   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
[5]   Two different but converging messenger pathways to intracellular Ca2+ release:: the roles of nicotinic acid adenine dinucleotide phosphate, cyclic ADP-ribose and inositol trisphosphate [J].
Cancela, JM ;
Gerasimenko, OV ;
Gerasimenko, JV ;
Tepikin, AV ;
Petersen, OH .
EMBO JOURNAL, 2000, 19 (11) :2549-2557
[6]  
Cheng JF, 2001, J AM SOC NEPHROL, V12, P54, DOI 10.1681/ASN.V12154
[7]  
Chini E. N., 1996, FASEB Journal, V10, pA143
[8]   Differential effect of pH upon cyclic-ADP-ribose and nicotinate adenine dinucleotide phosphate-induced Ca2+ release systems [J].
Chini, EN ;
Liang, MY ;
Dousa, TP .
BIOCHEMICAL JOURNAL, 1998, 335 :499-504
[9]   Palmitoyl-CoA potentiates the Ca2+ release elicited by cyclic ADP-ribose [J].
Chini, EN ;
Dousa, TP .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (02) :C530-C537
[10]   Nicotinate-adenine dinucleotide phosphate-induced Ca2+ release does not behave as a Ca2+-induced Ca2+-release system [J].
Chini, EN ;
Dousa, TP .
BIOCHEMICAL JOURNAL, 1996, 316 :709-711