Small molecules that regulate lifespan: evidence for xenohormesis

被引:164
作者
Lamming, DW [1 ]
Wood, JG [1 ]
Sinclair, DA [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1111/j.1365-2958.2004.04209.x
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
Barring genetic manipulation, the diet known as calorie restriction (CR) is currently the only way to slow down ageing in mammals. The fact that CR works on most species, even microorganisms, implies a conserved underlying mechanism. Recent findings in the yeast Saccharomyces cerevisiae indicate that CR extends lifespan because it is a mild biological stressor that activates Sir2, a key component of yeast longevity and the founding member of the sirtuin family of deacetylases. The sirtuin family appears to have first arisen in primordial eukaryotes, possibly to help them cope with adverse conditions. Today they are found in plants, yeast, and animals and may underlie the remarkable health benefits of CR. Interestingly, a class of polyphenolic molecules produced by plants in response to stress can activate the sirtuins from yeast and metazoans. At least in the case of yeast, these molecules greatly extend lifespan by mimicking CR. One explanation for this surprising observation is the 'xenohormesis hypothesis', the idea that organisms have evolved to respond to stress signalling molecules produced by other species in their environment. In this way, organisms can prepare in advance for a deteriorating environment and/or loss of food supply.
引用
收藏
页码:1003 / 1009
页数:7
相关论文
共 42 条
[1]   Yeast life-span extension by calorie restriction is independent of NAD fluctuation [J].
Anderson, RM ;
Latorre-Esteves, M ;
Neves, AR ;
Lavu, S ;
Medvedik, O ;
Taylor, C ;
Howitz, KT ;
Santos, H ;
Sinclair, DA .
SCIENCE, 2003, 302 (5653) :2124-2126
[2]   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
[3]  
Ashrafi K, 2000, GENE DEV, V14, P1872
[4]   NAD+-dependent deacetylase Hst1p controls biosynthesis and cellular NAD+ levels in Saccharomyces cerevisiae [J].
Bedalov, A ;
Hirao, M ;
Posakony, J ;
Nelson, M ;
Simon, JA .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (19) :7044-7054
[5]   Identification of a small molecule inhibitor of Sir2p [J].
Bedalov, A ;
Gatbonton, T ;
Irvine, WP ;
Gottschling, DE ;
Simon, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :15113-15118
[6]   Longevity regulation in Saccharomyces cerevisiae:: Linking metabolism, genome stability, and heterochromatin [J].
Bitterman, KJ ;
Medvedik, O ;
Sinclair, DA .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (03) :376-+
[7]   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
[8]   Rtg2 protein links metabolism and genome stability in yeast longevity [J].
Borghouts, C ;
Benguria, A ;
Wawryn, J ;
Jazwinski, SM .
GENETICS, 2004, 166 (02) :765-777
[9]   Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase [J].
Brunet, A ;
Sweeney, LB ;
Sturgill, JF ;
Chua, KF ;
Greer, PL ;
Lin, YX ;
Tran, H ;
Ross, SE ;
Mostoslavsky, R ;
Cohen, HY ;
Hu, LS ;
Cheng, HL ;
Jedrychowski, MP ;
Gygi, SP ;
Sinclair, DA ;
Alt, FW ;
Greenberg, ME .
SCIENCE, 2004, 303 (5666) :2011-2015
[10]   Elimination of replication block protein Fob1 extends the life span of yeast mother cells [J].
Defossez, PA ;
Prusty, R ;
Kaeberlein, M ;
Lin, SJ ;
Ferrigno, P ;
Silver, PA ;
Keil, RL ;
Guarente, L .
MOLECULAR CELL, 1999, 3 (04) :447-455