NAD metabolism and sirtuins: Metabolic regulation of protein deacetylation in stress and toxicity

被引:132
作者
Yang, Tianle [1 ]
Sauve, Anthony A. [1 ]
机构
[1] Cornell Univ, Weill Med Ctr, Dept Pharmacol, New York, NY 10021 USA
关键词
sirtuins; Sir2; gene silencing; toxicity; genotoxins; longevity; NAD; metabolism; SIRT1;
D O I
10.1208/aapsj080472
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sirtuins are recently discovered NAD(+)-dependent deacetylases that remove acetyl groups from acetyllysine-modified proteins, thereby regulating the biological function of their targets. Sirtuins have been shown to increase organism and tissue survival in diverse organisms, ranging from yeast to mammals. Evidence indicates that NAD+ metabolism and sirtuins contribute to mechanisms that influence cell survival under conditions of stress and toxicity. For example, recent work has shown that sirtuins and increased NAD+ biosynthesis provide protection against neuron axonal degeneration initiated by genotoxicity or trauma. In light of their protective effects, sirtuins and NAD+ metabolism could represent therapeutic targets for treatment of acute and chronic neurodegenerative conditions. Our work has focused on elucidating the enzymatic functions of sirtuins and quantifying perturbations of cellular NAD+ metabolism. We have developed mass spectrometry methods to quantitate cellular NAD+ and nicotinamide. These methods allow the quantitation of changes in the amounts of these metabolites in cells caused by chemical and genetic interventions. Characterization of the biochemical properties of sirtuins and investigations of NAD+ metabolism are likely to provide new insights into mechanisms by which NAD+ metabolism regulates sirtuin activities in cells. To develop new strategies to improve cell stress resistance, we have initiated proof of concept studies on pharmacological approaches that target sirtuins and NAD+ metabolism, with the goal of enhancing cell protection against genotoxicity.
引用
收藏
页码:E632 / E643
页数:12
相关论文
共 77 条
[1]   Nicotinamide and PNC1 govern lifespan extension by calorie restriction in Saccharomyces cerevisiae [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Sinclair, DA .
NATURE, 2003, 423 (6936) :181-185
[2]   Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Cohen, H ;
Lin, SS ;
Manchester, JK ;
Gordon, JI ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18881-18890
[3]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[4]   Poly(ADP-ribosyl)ation inhibitors:: Promising drug candidates for a wide variety of pathophysiologic conditions [J].
Beneke, S ;
Diefenbach, J ;
Bürkle, A .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (06) :813-818
[5]   Discoveries of nicotinamide riboside as a nutrient and conserved NRK genes establish a Preiss-Handler independent route to NAD+ in fungi and humans [J].
Bieganowski, P ;
Brenner, C .
CELL, 2004, 117 (04) :495-502
[6]   Inhibition of silencing and accelerated aging by nicotinamide, a putative negative regulator of yeast Sir2 and human SIRT1 [J].
Bitterman, KJ ;
Anderson, RM ;
Cohen, HY ;
Latorre-Esteves, M ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :45099-45107
[7]   The Sir2 family of protein deacetylases [J].
Blander, G ;
Guarente, L .
ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 :417-435
[8]   Sirt1 regulates insulin secretion by repressing UCP2 in pancreatic β cells [J].
Bordone, L ;
Motta, MC ;
Picard, F ;
Robinson, A ;
Jhala, US ;
Apfeld, J ;
McDonagh, T ;
Lemieux, M ;
McBurney, M ;
Szilvasi, A ;
Easlon, EJ ;
Lin, SJ ;
Guarente, L .
PLOS BIOLOGY, 2006, 4 (02) :210-220
[9]   Mechanism of human SIRT1 activation by resveratrol [J].
Borra, MT ;
Smith, BC ;
Denu, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :17187-17195
[10]   SIRT1 deacetylation and repression of p300 involves lysine residues 1020/1024 within the cell cycle regulatory domain 1 [J].
Bouras, T ;
Fu, MF ;
Sauve, AA ;
Wang, F ;
Quong, AA ;
Perkins, ND ;
Hay, RT ;
Gu, W ;
Pestell, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (11) :10264-10276