ADP-ribosyl cyclases generate two unusual adenine homodinucleotides with cytotoxic activity on mammalian cells

被引:30
作者
Basile, G
Taglialatela-Scafati, O
Damonte, G
Armirotti, A
Bruzzone, S
Guida, L
Franco, L
Usai, C
Fattorusso, E
De Flora, A
Zocchi, E
机构
[1] Univ Genoa, Biochem Sect, Dept Expt Med, I-16132 Genoa, Italy
[2] Adv Biotechnol Ctr, I-16132 Genoa, Italy
[3] Univ Naples Federico II, Dept Chem & Nat Prod, I-80131 Naples, Italy
[4] Univ Genoa, Ctr Excellence Biomed Res, I-16132 Genoa, Italy
[5] CNR, Inst Biophys, I-16149 Genoa, Italy
关键词
adenylic dinucleotides; NAD(+); cyclic ADP-ribose; cytotoxicity;
D O I
10.1073/pnas.0503691102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ADP-ribosyl cyclases are ubiquitous enzymes responsible for synthesis from NAD+ of the intracellular calcium-releasing signal molecules cyclic ADP-ribose (cADPR) and nicotinic acid adenine dinucleotide phosphate (NAADP(+)). Here, we show that cyclases from lower and higher Metazoa also synthesize three adenylic dinucleotides from cADPR and adenine: diadenosine diphosphate and two isomers thereof. These dinucleoticles are present and metabolized in mammalian cells and affect intracellular calcium and cell proliferation. The diadenosine diphosphate isomers are naturally occurring nucleotides containing an N-glycosidic bond different from the usual C1'-N9. The identification of these members of the family of NAD(+)-derived, calcium-active nucleoticles opens new areas of investigation into their functional cooperation with cADPR and NAADP(+) and into their involvement in the physiology and pathology of calcium-controlled cell functions.
引用
收藏
页码:14509 / 14514
页数:6
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