Differential regulation of the intrinsic pathway of apoptosis in brain and liver during ageing

被引:22
作者
Stoka, Veronika
Turk, Vito
Bredesen, Dale E.
机构
[1] Jozef Stefan Inst, Dept Biochem & Mol Biol, Ljubljana 1000, Slovenia
[2] Buck Inst Age Res, Novato, CA 94945 USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
来源
FEBS LETTERS | 2006年 / 580卷 / 15期
关键词
age-dependent caspase activation; apoptosis-resistant tissues; cytochrome c/2 '-deoxyadenosine 5 '-triphosphate activation; intrinsic pathway; mitochondrial pathway; strain-dependent caspase activation;
D O I
10.1016/j.febslet.2006.05.066
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
The intrinsic (mitochondria-dependent) pathway of apoptosis is one of the major pathways leading to cell death. We evaluated cytochrome c/apoptotic protease activation factor-1 (Apaf-1)-dependent activation of caspase-3 in brain and liver of different strains of rodents at different stages of development. In cell-free extracts from brain and liver of Sprague-Dawley rats, caspase was activated by cytochrome c/2'-deoxyadenosine 5'-triphosphate at both neonatal and adult stages. In adult brain extracts from Wistar rats, no activation of caspase was observed while extracts from neonatal brain and liver and from adult liver were activated. In CD-I mouse, only neonatal extracts were activated. Alteration in levels of endogenous inhibitors of apoptosis were not responsible for the lack of activation observed. Instead, decrease in the content of Apaf-1 and caspase-3 and some degradation of caspase-9 during brain ageing were observed. These results suggest that a decrease in apoptosis activation during ageing is not tissue-specific, but rather displays a complex dependence on species and strains of animals. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3739 / 3745
页数:7
相关论文
共 41 条
[1]   The mitochondrial apoptosome: a killer unleashed by the cytochrome seas [J].
Adrain, C ;
Martin, SJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (06) :390-397
[2]   Caspase-3 cleaves Apaf-1 into an ∼30 kDa fragment that associates with an inappropriately oligomerized and biologically inactive ∼1.4 MDa apoptosome complex [J].
Bratton, SB ;
Walker, G ;
Roberts, DL ;
Cain, K ;
Cohen, GM .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (04) :425-433
[3]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[4]   Human skeletal muscle cytosols are refractory to cytochrome c-dependent activation of type-II caspases and lack APAF-1 [J].
Burgess, DH ;
Svensson, M ;
Dandrea, T ;
Grönlund, K ;
Hammarquist, F ;
Orrenius, S ;
Cotgreave, IA .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (03) :256-261
[5]   Evidence for genetic modifiers of ovarian follicular endowment and development from studies of five inbred mouse strains [J].
Canning, J ;
Takai, Y ;
Tilly, JL .
ENDOCRINOLOGY, 2003, 144 (01) :9-12
[6]   Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development [J].
Cecconi, F ;
Alvarez-Bolado, G ;
Meyer, BI ;
Roth, KA ;
Gruss, P .
CELL, 1998, 94 (06) :727-737
[7]   Cell death: Critical control points [J].
Danial, NN ;
Korsmeyer, SJ .
CELL, 2004, 116 (02) :205-219
[8]   ACTIVATION OF THE APOPTOTIC PROTEASE CPP32 BY CYTOTOXIC T-CELL-DERIVED GRANZYME-B [J].
DARMON, AJ ;
NICHOLSON, DW ;
BLEACKLEY, RC .
NATURE, 1995, 377 (6548) :446-448
[9]   Drugs targeting mitochondrial functions to control tumor cell growth [J].
Dias, N ;
Bailly, C .
BIOCHEMICAL PHARMACOLOGY, 2005, 70 (01) :1-12
[10]   Apoptosis-resistance of hypoxic cells - Multiple factors involved and a role for IAP-2 [J].
Dong, Z ;
Wang, JZ ;
Yu, FS ;
Venkatachalam, MA .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (02) :663-671