C. elegans longevity pathways converge to decrease mitochondrial membrane potential

被引:64
作者
Lemire, Bernard D. [1 ]
Behrendt, Maciej [1 ]
DeCorby, Adrienne [1 ]
Gaskova, Dana [2 ]
机构
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[2] Charles Univ Prague, Fac Math & Phys, Inst Phys, CR-12116 Prague 2, Czech Republic
基金
加拿大健康研究院;
关键词
Mitochondria; Aging; Bioenergetics; Uncoupler; Lifespan; RNA interference; SYSTEMATIC RNAI SCREEN; EXTENDS LIFE-SPAN; CAENORHABDITIS-ELEGANS; OXIDATIVE STRESS; LONG; GENES; MUTANTS; MICE; DAMAGE; MODEL;
D O I
10.1016/j.mad.2009.05.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Energy production via oxidative phosphorylation generates a mitochondrial membrane potential (Delta Psi(m)) across the inner membrane. In this work, we show that a lower Delta Psi(m) is associated with increased lifespan in Caenorhabditis elegans. The long-lived mutants daf-2(ei370), age-1(hx546), clk-1(qm30), isp-1(qm150) and eat-2(ad465) all have a lower Delta Psi(m) than wild type animals. The lower Delta Psi(m) of daf-2(e1370) is daf-16 dependent, indicating that the insulin-like signaling pathway not only regulates lifespan but also mitochondrial energetics. RNA interference (RNAi) against 17 genes shown to extend lifespan also decrease Delta Psi(m). Furthermore, lifespan can be significantly extended with the uncoupler carbonylcyanide-3-chlorophenylhydrazone (CCCP), which dissipates Delta Psi(m). We conclude that longevity pathways converge on the mitochondria and lead to a decreased Delta Psi(m). Our results are consistent with the uncoupling to survive hypothesis, which states that dissipation of the Delta Psi(m) will extend lifespan. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:461 / 465
页数:5
相关论文
共 45 条
[1]   Higher respiratory activity decreases mitochondrial reactive oxygen release and increases life span in Saccharomyces cerevisiae [J].
Barros, MH ;
Bandy, B ;
Tahara, EB ;
Kowaltowski, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49883-49888
[2]   Apparent uncoupling of energy production and consumption in long-lived Clk mutants of Caenorhabditis elegans [J].
Braeckman, BP ;
Houthoofd, K ;
De Vreese, A ;
Vanfleteren, JR .
CURRENT BIOLOGY, 1999, 9 (09) :493-496
[3]   Uncoupling to survive? The role of mitochondrial inefficiency in ageing [J].
Brand, MD .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (6-7) :811-820
[4]   Testing the rate-of-living/oxidative damage theory of aging in the nematode model Caenorhabditis elegans [J].
Brys, Kristel ;
Vanfleteren, Jacques R. ;
Braeckman, Bart P. .
EXPERIMENTAL GERONTOLOGY, 2007, 42 (09) :845-851
[5]   Longevity determined by developmental arrest genes in Caenorhabditis elegans [J].
Chen, Di ;
Pan, Kally Z. ;
Palter, Julia E. ;
Kapahi, Pankaj .
AGING CELL, 2007, 6 (04) :525-533
[6]   Lifespan regulation by evolutionarily conserved genes essential for viability [J].
Curran, Sean P. ;
Ruvkun, Gary .
PLOS GENETICS, 2007, 3 (04) :0479-0487
[7]   Mild mitochondrial uncoupling in mice affects energy metabolism, redox balance and longevity [J].
da Silva, Camille C. Caldeira ;
Cerqueira, Fernanda M. ;
Barbosa, Livea F. ;
Medeiros, Marisa H. G. ;
Kowaltowski, Alicia J. .
AGING CELL, 2008, 7 (04) :552-560
[8]   Expression of Ndi1p, an alternative NADH:ubiquinone oxidoreductase, increases mitochondrial membrane potential in a C elegans model of mitochondrial disease [J].
DeCorby, Adrienne ;
Gaskova, Dana ;
Sayles, Leanne C. ;
Lernire, Bernard D. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2007, 1767 (09) :1157-1163
[9]   Rates of behavior and aging specified by mitochondrial function during development [J].
Dillin, A ;
Hsu, AL ;
Arantes-Oliveira, NA ;
Lehrer-Graiwer, J ;
Hsin, H ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Kenyon, C .
SCIENCE, 2002, 298 (5602) :2398-2401
[10]   DiS-C3(3) monitoring of in vivo mitochondrial membrane potential in C-elegans [J].
Gaskova, Dana ;
DeCorby, Adrienne ;
Lemire, Bernard D. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 354 (03) :814-819