Accelerated aging-related transcriptome changes in the female prefrontal cortex

被引:28
作者
Yuan, Yuan [1 ,2 ]
Chen, Yi-Ping Phoebe [2 ]
Boyd-Kirkup, Jerome [1 ]
Khaitovich, Philipp [1 ,3 ]
Somel, Mehmet [1 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Key Lab Computat Biol, CAS MPG Partner Inst Computat Biol, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
[2] La Trobe Univ, Dept Comp Sci & Comp Engn, Melbourne, Vic 3086, Australia
[3] Max Planck Inst Evolutionary Anthropol, D-04103 Leipzig, Germany
[4] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; central nervous system; gene expression; prefrontal cortex; sex difference; EXPRESSION TIME-SERIES; ALZHEIMERS-DISEASE; GENE-EXPRESSION; SEX-DIFFERENCES; HUMAN BRAIN; GENDER-DIFFERENCES; MAJOR DEPRESSION; TAU PATHOLOGY; STRESS; DEMENTIA;
D O I
10.1111/j.1474-9726.2012.00859.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human female life expectancy is higher than that of males. Intriguingly, it has been reported that women display faster rates of age-related cognitive decline and a higher prevalence of Alzheimers disease (AD). To assess the molecular bases of these contradictory trends, we analyzed differences in expression changes with age between adult males and females, in four brain regions. In the superior frontal gyrus (SFG), a part of the prefrontal cortex, we observed manifest differences between the two sexes in the timing of age-related changes, that is, sexual heterochrony. Intriguingly, age-related expression changes predominantly occurred earlier, or at a faster pace, in females compared to men. These changes included decreased energy production and neural function and up-regulation of the immune response, all major features of brain aging. Furthermore, we found that accelerated expression changes in the female SFG correlated with expression changes observed in AD, as well as stress effects in the frontal cortex. Accelerated aging-related changes in the female SFG transcriptome may provide a link between a higher stress exposure or sensitivity in women and the higher prevalence of AD.
引用
收藏
页码:894 / 901
页数:8
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