Age-related impairment of the transcriptional responses to oxidative stress in the mouse heart

被引:63
作者
Edwards, MG
Sarkar, D
Klopp, R
Morrow, JD
Weindruch, R
Prolla, TA [1 ]
机构
[1] Univ Wisconsin, Dept Genet & Med Genet, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Stat, Madison, WI 53706 USA
[3] Univ Wisconsin, Vet Adm Hosp, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Med, Madison, WI 53706 USA
[5] Univ Wisconsin, Wisconsin Primate Res Ctr, Madison, WI 53706 USA
[6] Vanderbilt Univ, Dept Med & Pharmacol, Nashville, TN 37232 USA
关键词
aging; paraquat; gene expression;
D O I
10.1152/physiolgenomics.00172.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To investigate the transcriptional response to oxidative stress in the heart and how it changes with age, we examined the cardiac gene expression profiles of young (5-mo-old), middle-aged (15-mo-old), and old (25-mo-old) C57BL/6 mice treated with a single intraperitoneal injection of paraquat ( 50 mg/ kg). Mice were killed at 0, 1, 3, 5, and 7 h after paraquat treatment, and the gene expression profile was obtained with high-density oligonucleotide microarrays. Of 9,977 genes represented on the microarray, 249 transcripts in the young mice, 298 transcripts in the middle-aged mice, and 256 transcripts in the old mice displayed a significant change in mRNA levels (ANOVA, P < 0.01). Among these, a total of 55 transcripts were determined to be paraquat responsive for all age groups. Genes commonly induced in all age groups include those associated with stress, inflammatory, immune, and growth factor responses. Interestingly, only young mice displayed a significant increase in expression of all three isoforms of GADD45, a DNA damage-responsive gene. Additionally, the number of immediate early response genes (IEGs) found to be induced by paraquat was considerably higher in the younger animals. These results demonstrate that, at the transcriptional level, there is an age-related impairment of specific inducible pathways in the response to oxidative stress in the mouse heart.
引用
收藏
页码:119 / 127
页数:9
相关论文
共 54 条
[1]   Induction of metallothionein by zinc protects from daunorubicin toxicity in rats [J].
Ali, MM ;
Frei, E ;
Straub, J ;
Breuer, A ;
Wiessler, M .
TOXICOLOGY, 2002, 179 (1-2) :85-93
[2]   Paraquat induces different pulmonary biochemical responses in Wistar rats and Swiss mice [J].
Ali, S ;
Diwakar, G ;
Pawa, S .
CHEMICO-BIOLOGICAL INTERACTIONS, 2000, 125 (02) :79-91
[3]   Direct activation of mitochondrial apoptosis machinery by c-Jun N-terminal kinase in adult cardiac myocytes [J].
Aoki, H ;
Kang, PM ;
Hampe, J ;
Yoshimura, K ;
Noma, T ;
Matsuzaki, M ;
Izumo, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (12) :10244-10250
[4]   Calcineurin regulates ryanodine receptor/Ca2+-release channels in rat heart [J].
Bandyopadhyay, A ;
Shin, DW ;
Ahn, JO ;
Kim, DH .
BIOCHEMICAL JOURNAL, 2000, 352 :61-70
[5]   Coordinate expression of the PDK4 gene: a means of regulating fuel selection in a hibernating mammal [J].
Buck, MJ ;
Squire, TL ;
Andrews, MT .
PHYSIOLOGICAL GENOMICS, 2002, 8 (01) :5-13
[6]   Metallothionein in radiation exposure: its induction and protective role [J].
Cai, L ;
Satoh, M ;
Tohyama, C ;
Cherian, MG .
TOXICOLOGY, 1999, 132 (2-3) :85-98
[7]   Homocysteine-responsive ATF3 gene expression in human vascular endothelial cells:: activation of c-Jun NH2-terminal kinase and promoter response element [J].
Cai, Y ;
Zhang, C ;
Nawa, T ;
Aso, T ;
Tanaka, M ;
Oshiro, S ;
Ichijo, H ;
Kitajima, S .
BLOOD, 2000, 96 (06) :2140-2148
[8]   Increased binding activity at an antioxidant-responsive element in the metallothionein-1 promoter and rapid induction of metallothionein-1 and-2 in response to cerebral ischemia and reperfusion [J].
Campagne, MV ;
Thibodeaux, H ;
van Bruggen, N ;
Cairns, B ;
Lowe, DG .
JOURNAL OF NEUROSCIENCE, 2000, 20 (14) :5200-5207
[9]   Mitogen-activated protein kinase cascades and the signaling of hyperosmotic stress to immediate early genes [J].
Cohen, DM .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1997, 117 (03) :291-299
[10]   Paraquat: A useful tool for the in vivo study of mechanisms of neuronal cell death [J].
Corasaniti, MT ;
Strongoli, MC ;
Rotiroti, D ;
Bagetta, G ;
Nistico, G .
PHARMACOLOGY & TOXICOLOGY, 1998, 83 (01) :1-7