Compartmentation of NAD+-dependent signalling

被引:108
作者
Koch-Nolte, Friedrich [1 ]
Fischer, Stefan [2 ]
Haag, Friedrich [1 ]
Ziegler, Mathias [2 ]
机构
[1] Univ Med Ctr, Inst Immunol, D-20246 Hamburg, Germany
[2] Univ Bergen, Dept Mol Biol, N-5008 Bergen, Norway
关键词
NAD(+); ADP-ribosyltransferase; Sirtuins; NAD(+) glycohydrolase; NAD(+) signalling; NICOTINAMIDE ADENINE-DINUCLEOTIDE; NAADP MOBILIZES CALCIUM; ADP-RIBOSYLATION; CRYSTAL-STRUCTURES; T-CELLS; NAD(+); PROTEIN; POLY(ADP-RIBOSE); BINDING; CD38;
D O I
10.1016/j.febslet.2011.03.045
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
NAD(+) plays central roles in energy metabolism as redox carrier. Recent research has identified important signalling functions of NAD(+) that involve its consumption. Although NAD(+) is synthesized mainly in the cytosol, nucleus and mitochondria, it has been detected also in vesicular and extracellular compartments. Three protein families that consume NAD(+) in signalling reactions have been characterized on a molecular level: ADP-ribosyltransferases (ARTs), Sirtuins (SIRTs), and NAD(+) glycohydrolases (NADases). Members of these families serve important regulatory functions in various cellular compartments, e. g., by linking the cellular energy state to gene expression in the nucleus, by regulating nitrogen metabolism in mitochondria, and by sensing tissue damage in the extracellular compartment. Distinct NAD(+) pools may be crucial for these processes. Here, we review the current knowledge about the compartmentation and biochemistry of NAD(+)-converting enzymes that control NAD+ signalling. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1651 / 1656
页数:6
相关论文
共 63 条
[1]   ADP-ribosylation at R125 gates the P2X7 ion channel by presenting a covalent ligand to its nucleotide binding site [J].
Adriouch, Sahil ;
Bannas, Peter ;
Schwarz, Nicole ;
Fliegert, Ralf ;
Guse, Andreas H. ;
Seman, Michel ;
Haag, Friedrich ;
Koch-Nolte, Friedrich .
FASEB JOURNAL, 2008, 22 (03) :861-869
[2]   NAD+ released during inflammation participates in T cell homeostasis by inducing ART2-mediated death of naive T cells in vivo [J].
Adriouch, Sahil ;
Hubert, Sandra ;
Pechberty, Severine ;
Koch-Nolte, Friedrich ;
Haag, Friedrich ;
Seman, Michel .
JOURNAL OF IMMUNOLOGY, 2007, 179 (01) :186-194
[3]   Mammalian circadian clock and metabolism - the epigenetic link [J].
Bellet, Marina Maria ;
Sassone-Corsi, Paolo .
JOURNAL OF CELL SCIENCE, 2010, 123 (22) :3837-3848
[4]   The new life of a centenarian:: signalling functions of NAD(P) [J].
Berger, F ;
Ramírez-Hernández, MH ;
Ziegler, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (03) :111-118
[5]   Essential requirement for two-pore channel 1 in NAADP-mediated calcium signaling [J].
Brailoiu, Eugen ;
Churamani, Dev ;
Cai, Xinjiang ;
Schrlau, Michael G. ;
Brailoiu, G. Cristina ;
Gao, Xin ;
Hooper, Robert ;
Boulware, Michael J. ;
Dun, Nae J. ;
Marchant, Jonathan S. ;
Patel, Sandip .
JOURNAL OF CELL BIOLOGY, 2009, 186 (02) :201-209
[6]  
Bruzzone S, 2001, FASEB J, V15, P10
[7]   NAADP mobilizes calcium from acidic organelles through two-pore channels [J].
Calcraft, Peter J. ;
Ruas, Margarida ;
Pan, Zui ;
Cheng, Xiaotong ;
Arredouani, Abdelilah ;
Hao, Xuemei ;
Tang, Jisen ;
Rietdorf, Katja ;
Teboul, Lydia ;
Chuang, Kai-Ting ;
Lin, Peihui ;
Xiao, Rui ;
Wang, Chunbo ;
Zhu, Yingmin ;
Lin, Yakang ;
Wyatt, Christopher N. ;
Parrington, John ;
Ma, Jianjie ;
Evans, A. Mark ;
Galione, Antony ;
Zhu, Michael X. .
NATURE, 2009, 459 (7246) :596-U130
[8]   PGC-1α, SIRT1 and AMPK, an energy sensing network that controls energy expenditure [J].
Canto, Carles ;
Auwerx, Johan .
CURRENT OPINION IN LIPIDOLOGY, 2009, 20 (02) :98-105
[9]   Functional aspects of protein mono-ADP-ribosylation [J].
Corda, D ;
Di Girolamo, M .
EMBO JOURNAL, 2003, 22 (09) :1953-1958
[10]   Molecular Mechanisms of the Cytotoxicity of ADP-Ribosylating Toxins [J].
Deng, Qing ;
Barbieri, Joseph T. .
ANNUAL REVIEW OF MICROBIOLOGY, 2008, 62 :271-288