A new function for CD38/ADP-ribosyl cyclase in nuclear Ca2+ homeostasis

被引:137
作者
Adebanjo, OA
Anandatheerthavarada, HK
Koval, AP
Moonga, BS
Biswas, G
Sun, L
Sodam, BR
Bevis, PJR
Huang, CLH
Epstein, S
Lai, FA
Avadhani, NG
Zaidi, M
机构
[1] CUNY Mt Sinai Sch Med, Div Endocrinol, New York, NY 10029 USA
[2] Med Coll Penn & Hahnemann Univ, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Vet Affairs Med Ctr, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
[5] Univ Cambridge, Physiol Lab, Cardiff CB2 3EG, S Glam, Wales
[6] Univ Wales, Coll Med, Cardiff CF14 4XN, S Glam, Wales
关键词
D O I
10.1038/15640
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nucleoplasmic calcium ions (Ca2+) influence nuclear functions as critical as gene transcription, apoptosis, DNA repair, topoisomerase activation and polymerase unfolding. Although both inositol trisphosphate receptors and ryanodine receptors, types of Ca2+ channel, are present in the nuclear membrane, their role in the homeostasis of nuclear Ca2+ remains unclear. Here we report the existence in the inner nuclear membrane of a functionally active CD38/ADP-ribosyl cyclase that has its catalytic site within the nucleoplasm. We propose that the enzyme catalyses the intranuclear cyclization of nicotinamide adenine dinucleotide to cyclic adenosine diphosphate ribose. The latter activates ryanodine receptors of the inner nuclear membrane to trigger nucleoplasmic Ca2+ release.
引用
收藏
页码:409 / 414
页数:6
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