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1
Differential regulation of nicotinic acid-adenine dinucleotide phosphate and cADP-ribose production by cAMP and cGMP.环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)对磷酸烟酰胺腺嘌呤二核苷酸(NAADP)和环ADP核糖(cADP-核糖)生成的差异调节
Biochem J. 1998 May 1;331 ( Pt 3)(Pt 3):837-43. doi: 10.1042/bj3310837.
2
Cyclic GMP-dependent and -independent effects on the synthesis of the calcium messengers cyclic ADP-ribose and nicotinic acid adenine dinucleotide phosphate.环磷酸鸟苷依赖性和非依赖性对钙信使环ADP-核糖和烟酰胺腺嘌呤二核苷酸磷酸合成的影响。
J Biol Chem. 1998 Jan 2;273(1):118-25. doi: 10.1074/jbc.273.1.118.
3
Differential effect of pH upon cyclic-ADP-ribose and nicotinate-adenine dinucleotide phosphate-induced Ca2+ release systems.pH对环ADP核糖和烟酸腺嘌呤二核苷酸磷酸诱导的Ca2+释放系统的差异作用。
Biochem J. 1998 Nov 1;335 ( Pt 3)(Pt 3):499-504. doi: 10.1042/bj3350499.
4
Interactions between intracellular Ca2+ stores: Ca2+ released from the NAADP pool potentiates cADPR-induced Ca2+ release.细胞内钙库之间的相互作用:从NAADP池释放的Ca2+增强了cADPR诱导的Ca2+释放。
Braz J Med Biol Res. 2002 May;35(5):543-7. doi: 10.1590/s0100-879x2002000500005.
5
Adenine nucleotide diphosphates: emerging second messengers acting via intracellular Ca2+ release.腺嘌呤核苷二磷酸:通过细胞内钙离子释放发挥作用的新兴第二信使。
Am J Physiol. 1996 Oct;271(4 Pt 1):C1007-24. doi: 10.1152/ajpcell.1996.271.4.C1007.
6
Mechanisms of calcium signaling by cyclic ADP-ribose and NAADP.环ADP核糖和NAADP介导钙信号传导的机制
Physiol Rev. 1997 Oct;77(4):1133-64. doi: 10.1152/physrev.1997.77.4.1133.
7
NAADP induces Ca2+ oscillations via a two-pool mechanism by priming IP3- and cADPR-sensitive Ca2+ stores.烟酰胺腺嘌呤二核苷酸磷酸(NAADP)通过启动对三磷酸肌醇(IP3)和环磷酸腺苷二磷酸核糖(cADPR)敏感的钙离子储存库,经由双池机制诱导钙离子振荡。
EMBO J. 2001 Jun 1;20(11):2666-71. doi: 10.1093/emboj/20.11.2666.
8
A derivative of NADP mobilizes calcium stores insensitive to inositol trisphosphate and cyclic ADP-ribose.烟酰胺腺嘌呤二核苷酸磷酸(NADP)的一种衍生物可动员对肌醇三磷酸和环二磷酸腺苷核糖不敏感的钙库。
J Biol Chem. 1995 Feb 3;270(5):2152-7. doi: 10.1074/jbc.270.5.2152.
9
Differential effect of glycolytic intermediaries upon cyclic ADP-ribose-, inositol 1',4',5'-trisphosphate-, and nicotinate adenine dinucleotide phosphate-induced Ca(2+) release systems.糖酵解中间产物对环ADP核糖、肌醇1',4',5'-三磷酸和烟酰胺腺嘌呤二核苷酸磷酸诱导的Ca(2+)释放系统的差异作用。
Arch Biochem Biophys. 1999 Oct 15;370(2):294-9. doi: 10.1006/abbi.1999.1373.
10
Role of Ins(1,4,5)P3, cADP-ribose and nicotinic acid-adenine dinucleotide phosphate in Ca2+ signalling in mouse submandibular acinar cells.肌醇-1,4,5-三磷酸、环二磷酸腺苷核糖和烟酸腺嘌呤二核苷酸磷酸在小鼠下颌下腺腺泡细胞钙信号传导中的作用
Biochem J. 2001 Feb 1;353(Pt 3):555-60. doi: 10.1042/0264-6021:3530555.

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NAADP-Mediated Ca Signalling.NAADP介导的钙信号传导。
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Adenylate Cyclase 1 Links Calcium Signaling to CFTR-Dependent Cytosolic Chloride Elevations in Chick Amacrine Cells.腺苷酸环化酶1将钙信号与鸡无长突细胞中CFTR依赖的胞质氯化物升高联系起来。
Front Cell Neurosci. 2021 Aug 11;15:726605. doi: 10.3389/fncel.2021.726605. eCollection 2021.
3
ADP-ribosyl cyclases regulate early development of the sea urchin.ADP核糖基环化酶调节海胆的早期发育。
Messenger (Los Angel). 2016 Jun 1;5(1-2):100-106. doi: 10.1166/msr.2016.1052.
4
cAMP-dependent recruitment of acidic organelles for Ca2+ signaling in the salivary gland.环磷酸腺苷(cAMP)依赖性酸性细胞器募集参与唾液腺中的钙离子(Ca2+)信号传导。
Am J Physiol Cell Physiol. 2016 Nov 1;311(5):C697-C709. doi: 10.1152/ajpcell.00010.2016. Epub 2016 Sep 7.
5
Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) and Cyclic ADP-Ribose (cADPR) Mediate Ca2+ Signaling in Cardiac Hypertrophy Induced by β-Adrenergic Stimulation.烟酰胺腺嘌呤二核苷酸磷酸(NAADP)和环二磷酸腺苷核糖(cADPR)介导β-肾上腺素能刺激诱导的心肌肥大中的Ca2+信号传导。
PLoS One. 2016 Mar 9;11(3):e0149125. doi: 10.1371/journal.pone.0149125. eCollection 2016.
6
Nicotinic acid modulates intracellular calcium concentration and disassembles the cytoskeleton.烟酸调节细胞内钙浓度并分解细胞骨架。
Mol Med Rep. 2014 Dec;10(6):2805-10. doi: 10.3892/mmr.2014.2576. Epub 2014 Sep 18.
7
Generation of cyclic ADP-ribose and nicotinic acid adenine dinucleotide phosphate by CD38 for Ca2+ signaling in interleukin-8-treated lymphokine-activated killer cells.CD38在白细胞介素-8处理的淋巴因子激活的杀伤细胞中生成环磷酸腺苷核糖和烟酰胺腺嘌呤二核苷酸磷酸用于Ca2+信号传导
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8
Ca(2+) signaling occurs via second messenger release from intraorganelle synthesis sites.钙离子(Ca²⁺)信号传导通过细胞器内合成位点释放第二信使来实现。
Curr Biol. 2008 Oct 28;18(20):1612-8. doi: 10.1016/j.cub.2008.09.024.
9
Molecular characterization of a novel cell surface ADP-ribosyl cyclase from the sea urchin.一种来自海胆的新型细胞表面ADP-核糖基环化酶的分子特征
Cell Signal. 2008 Dec;20(12):2347-55. doi: 10.1016/j.cellsig.2008.09.005. Epub 2008 Sep 13.
10
Sperm express a Ca2+-regulated NAADP synthase.精子表达一种钙离子调节的烟酰胺腺嘌呤二磷酸核糖(NAADP)合酶。
Biochem J. 2008 Apr 1;411(1):63-70. doi: 10.1042/BJ20071616.

本文引用的文献

1
Mechanisms of calcium signaling by cyclic ADP-ribose and NAADP.环ADP核糖和NAADP介导钙信号传导的机制
Physiol Rev. 1997 Oct;77(4):1133-64. doi: 10.1152/physrev.1997.77.4.1133.
2
The CD38 lymphocyte differentiation marker: new insight into its ectoenzymatic activity and its role as a signal transducer.CD38淋巴细胞分化标志物:对其胞外酶活性及其作为信号转导分子作用的新认识。
Immunity. 1997 Sep;7(3):315-24. doi: 10.1016/s1074-7613(00)80353-2.
3
Stimulation of cyclic ADP-ribose synthesis by acetylcholine and its role in catecholamine release in bovine adrenal chromaffin cells.乙酰胆碱对环ADP-核糖合成的刺激作用及其在牛肾上腺嗜铬细胞儿茶酚胺释放中的作用。
J Biol Chem. 1997 Aug 22;272(34):21002-9. doi: 10.1074/jbc.272.34.21002.
4
Pharmacological properties of the Ca2+-release mechanism sensitive to NAADP in the sea urchin egg.海胆卵中对NAADP敏感的Ca2+释放机制的药理学特性。
Br J Pharmacol. 1997 Aug;121(7):1489-95. doi: 10.1038/sj.bjp.0701295.
5
A Ca2+ release mechanism gated by the novel pyridine nucleotide, NAADP.一种由新型吡啶核苷酸NAADP门控的Ca2+释放机制。
Trends Pharmacol Sci. 1997 Apr;18(4):108-10. doi: 10.1016/s0165-6147(96)01036-x.
6
A specific cyclic ADP-ribose antagonist inhibits cardiac excitation-contraction coupling.一种特异性环二磷酸腺苷核糖拮抗剂可抑制心脏兴奋-收缩偶联。
Curr Biol. 1996 Aug 1;6(8):989-96. doi: 10.1016/s0960-9822(02)00643-7.
7
Unique inactivation properties of NAADP-sensitive Ca2+ release.NAADP 敏感的 Ca2+ 释放的独特失活特性。
J Biol Chem. 1996 May 17;271(20):11599-602. doi: 10.1074/jbc.271.20.11599.
8
Nicotinic acid-adenine dinucleotide phosphate mobilizes Ca2+ from a thapsigargin-insensitive pool.烟酰胺腺嘌呤二核苷酸磷酸从毒胡萝卜素不敏感的储存库中动员钙离子。
Biochem J. 1996 May 1;315 ( Pt 3)(Pt 3):721-5. doi: 10.1042/bj3150721.
9
Activation and inactivation of Ca2+ release by NAADP+.NAADP+对Ca2+释放的激活与失活作用。
J Biol Chem. 1996 Apr 12;271(15):8513-6. doi: 10.1074/jbc.271.15.8513.
10
ADP-ribosyl cyclase and CD38 catalyze the synthesis of a calcium-mobilizing metabolite from NADP.ADP-核糖基环化酶和CD38催化从NADP合成一种可动员钙的代谢产物。
J Biol Chem. 1995 Dec 22;270(51):30327-33. doi: 10.1074/jbc.270.51.30327.

环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)对磷酸烟酰胺腺嘌呤二核苷酸(NAADP)和环ADP核糖(cADP-核糖)生成的差异调节

Differential regulation of nicotinic acid-adenine dinucleotide phosphate and cADP-ribose production by cAMP and cGMP.

作者信息

Wilson H L, Galione A

机构信息

University Department of Pharmacology, Oxford University, Mansfield Road, Oxford OX1 3QT, UK.

出版信息

Biochem J. 1998 May 1;331 ( Pt 3)(Pt 3):837-43. doi: 10.1042/bj3310837.

DOI:10.1042/bj3310837
PMID:9560312
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1219425/
Abstract

The sea urchin egg has been used as a system to study calcium-release mechanisms induced by inositol 1,4,5-trisphosphate (IP3), cADP-ribose (cADPR), and more recently, nicotinic acid-adenine dinucleotide phosphate (NAADP). In order that cADPR and NAADP may be established as endogenous messengers for calcium release, the existence of intracellular enzymes capable of metabolizing these molecules must be demonstrated. In addition, intracellular levels of cADPR and NAADP should be under the control of extracellular stimuli. It has been shown that cGMP stimulates the synthesis of cADPR in the sea urchin egg. The present study shows that the sea urchin egg is capable of synthesizing and degrading NAADP. cADPR and NAADP synthetic activities appear to be separate, with different cellular localizations, pH and temperature optima. We suggest that in the sea urchin egg, cADPR and NAADP production may be differentially regulated by receptor-coupled second messengers, with cADPR production being regulated by cGMP and NAADP production modulated by cAMP.

摘要

海胆卵已被用作一个系统来研究由肌醇1,4,5 -三磷酸(IP3)、环ADP -核糖(cADPR)以及最近的烟酸腺嘌呤二核苷酸磷酸(NAADP)诱导的钙释放机制。为了使cADPR和NAADP能够被确立为钙释放的内源性信使,必须证明存在能够代谢这些分子的细胞内酶。此外,cADPR和NAADP的细胞内水平应该受到细胞外刺激的控制。已经表明,cGMP刺激海胆卵中cADPR的合成。本研究表明海胆卵能够合成和降解NAADP。cADPR和NAADP的合成活性似乎是分开的,具有不同的细胞定位、最适pH值和温度。我们认为在海胆卵中,cADPR和NAADP的产生可能受到受体偶联的第二信使的差异调节,cADPR的产生由cGMP调节,而NAADP的产生由cAMP调节。