Molecular Nutrition

Ca2+ Release Mechanisms Mediated by Cyclic Adenosine Diphosphoribose as a Second Messenger

Expand
  • 1. Animal Nutrition Institute, Sichuan Agricultural University, Ya'an 625014, China;
    2. Fish Nutrition and Safety in Production Sichuan University Key Laboratary, Sichuan Agricultural University, Ya'an 625014, China;
    3. Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Ya'an 625014, China

Received date: 2011-06-27

  Online published: 2011-12-14

Abstract

Cyclic ADP-ribose (cADPR) is a Ca2+ mobilizing second messenger in various types of cell, tissue and organism. cADPR regulates the release of Ca2+ depending on the gating properties of ryanodine receptors (RyRs), which is transmembrane shuttling of the substrate coenzyme Ⅰ (NAD+) and the product cADPR, or ligand-induced internalization of CD38. This review summarizes mechanisms of cADPR synthesis and its regulation on intracellular Ca2+ release.

Cite this article

LI Xueyin, FENG Lin, LIU Yang, JIANG Jun, ZHOU Xiaoqiu . Ca2+ Release Mechanisms Mediated by Cyclic Adenosine Diphosphoribose as a Second Messenger[J]. Chinese Journal of Animal Nutrition, 2011 , 23(12) : 2043 -2047 . DOI: 10.3969/j.issn.1006-267x.2011.12.001

References

[1] LEE H C, WALSETH T F, BRATT G T, et al. Structural determination of a cyclic metabolite of NAD+ with intracellular Ca2+-mobilizing activity[J]. Journal of Biological Chemistry, 1989, 264(3):1608-1615.



[2] BARONE F, GENAZZANI A A, COMTI A, et al. A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells[J]. The FASEB Journal, 2002, 16(7):697-705.  



[3] BECK A, KOLISEK M, BAGLEY L A, et al. Nicotinic acid adenine dinucleotide phosphate and cyclic ADP-ribose regulate TRPM2 channels in T lymphocytes[J]. The FASEB Journal, 2006, 20(7):962-964.  



[4] WILSON H L, DIPP M, THOMAS J, et al. ADP-ribosyl cyclase and cyclic ADP-ribose hydrolase act as a redox sensor[J]. Journal of Biological Chemistry, 2001, 276(14):11180-11188.  



[5] YUE J, WEI W , LAM C M C, et al. CD38/cADPR/Ca pathway promotes cell proliferation and elays nerve growth factor-induced differentiation in PC12 cells[J]. Journal of Biological Chemistry, 2009, 284(43):29335-39442.  



[6] LEE H C, AARHUS R, LEVITT D. The crystal structure of cyclic ADP-ribose[J]. Nature Structural & Molecular Biology, 1994, 1(3):143-144.  



[7] GUSE A H, CAKIR-KIEFER C, FUKUOKA M, et al. Novel hydrolysis-resistant analogues of cyclic ADP-ribose: modification of the 'northern' ribose and calcium release activity[J]. Biochemistry, 2002, 41(2):6744-6751.  



[8] LEE H C. Structure and enzymatic functions of human CD38[J]. Molecular Medicine, 2006, 12(11/12):317-323.



[9] FUNARO A, REINIS M, TRUBIANI O, et al. CD38 functions are regulated through an internalization step[J]. The Journal of Immunology, 1998, 160(5):2238-2247.



[10] DE FLORA A, GUIDA FRANCO L, ZOCCHI E, et al. Ectocellular in vitro and in vivo metabolism of cyclic ADP-ribose in cerebellum[J]. Biochemistry, 1996, 320:665-672.



[11] BRUZZONE S, GUIDA L, ZOCCHI E, et al. Connexin 43 hemichannels mediate Ca2+-regulated transmembrane NAD+ fluxes in intact cells[J]. The FASEB Journal, 2000, 15(1):10-12.



[12] BRUZZONE S, FRANCO L, GUIDA L, et al. A self-restricted CD38-connexin 43 cross-talk affects NAD+ and cyclic ADP-ribose metabolism and regulates intracellular calcium in 3T3 fibroblasts[J]. Journal of Biological Chemistry, 2001, 276(51):48300-48308.



[13] LI P L, TANG W X, VALDIVIA H H, et al. cADP-ribose activates reconstituted ryanodine receptors from coronary arterial smooth muscle[J]. Heart and Circulatory Physiology, 2001, 280(1):208-215.



[14] FRANCO L, GUIDA L, BRUZZONE S, et al. The transmembrane glycoprotein CD38 is a catalytically active transporter responsible for generation and influx of the second messenger cyclic ADP-ribose across membranes [J]. The FASEB Journal, 1998, 12(14):1507-1520.



[15] SHAHID U, MALAVASI F, MEHTA K. Post-translational modification of CD38 protein into a high molecular weight form alters its catalytic properties[J]. Journal of Biological Chemistry, 1996, 271(21):15922-15927.



[16] RAH S Y, PARK K H, NAM T S, et al. Association of CD38 with nonmuscle myosin heavy chain ⅡA and Lck is essential for the internalization and activation of CD38[J]. Journal of Biological Chemistry, 2007, 282(14):5653-5660.



[17] ZOCCHI E, USAI C, GUIDA L, et al. Ligand-induced internalization of CD38 results in intracellular Ca2+ mobilization: role of NAD+ transport across cell membranes[J]. The FASEB Journal, 1999, 13(2):273-283.



[18] HAN M K, KIM S J , PARK Y R. Antidiabetic effect of a prodrug of cysteine, L-2-oxothiazolidine-4-carboxylic acid, through CD38 dimerization and internalization[J]. Journal of Biological Chemistry, 2002, 277(7):5315-5321.  



[19] TANG W X, CHEN Y F, ZOU A P. Role of FKBP12.6 in cADPR-induced activation of reconstituted ryanodine receptors from arterial smooth muscle[J]. Heart Circle Physiological, 2002, 282(4):H1304-H1310.



[20] WANG Y X, ZHENG Y M, MEI Q B, et al. FKBP12.6 and cADPR regulation of Ca2+ release in smooth muscle cells[J]. Cell Physiology, 2004, 286(3):C538-C546.



[21] FRUEN B R, MICKELSON J R, SHOMER N H, et al. Cyclic ADP-ribose does not affect cardiac or skeletal muscle ryanodine receptors[J]. FEBS Letters, 1994, 352(2):123-126.  



[22] WAGENKNECHT T, RADERMACHER M, GRASSUCCI R, et al. Locations of calmodulin and FK506-binding protein on the three-dimensional architecture of the skeletal muscle ryanodine receptor[J]. Journal of Biological Chemistry, 1997, 272(51):32463-32471.  



[23] JI G, FELDMAN M E, GREENE K S, et al. RYR2 proteins contribute to the formation of Ca2+ sparks in smooth muscle[J]. General Physiology, 2004, 123(4):377-386.  



[24] THOMAS J M, SUMMERHILL R J, FRUEN B R, et al. Calmodulin dissociation mediates desensitization of the cADPR-induced Ca2+ release mechanism[J]. Current Biology, 2002, 12(23):2018-2022.  



[25] BALSHAW D M, XU L, YAMAGUCHI N, et al. Calmodulin binding and inhibition of cardiac muscle calcium release channel (ryanodine receptor)[J]. Journal of Biological chemistry, 2001, 276(23):20144-20153.  
Outlines

/