Impairment of the transcriptional responses to oxidative stress in the heart of aged C57BL/6 mice

被引:19
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] Vanderbilt Univ, Dept Pharmacol & Med, Nashville, TN 37232 USA
[5] Univ Wisconsin, Dept Med, Madison, WI 53706 USA
[6] Univ Wisconsin, Wisconsin Primate Res Ctr, Madison, WI 53706 USA
来源
STRATEGIES FOR ENGINEERED NEGLIGIBLE SENESCENCE: WHY GENUINE CONTROL OF AGING MAY BE FORESEEABLE | 2004年 / 1019卷
关键词
aging; paraquat; gene expression;
D O I
10.1196/annals.1297.017
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
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 months old), middle-aged (15 months old), and old (25 months 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 hours 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 < .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 genes 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:85 / 95
页数:11
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