Apoptosis-related genes change their expression with age and hearing loss in the mouse cochlea

被引:89
作者
Tadros, Sherif F. [2 ]
D'Souza, Mary [1 ,3 ]
Zhu, Xiaoxia [1 ,3 ]
Frisina, Robert D. [1 ,3 ]
机构
[1] Univ Rochester, Dept Otolaryngol, Sch Med & Dent, Rochester, NY 14642 USA
[2] Univ New S Wales, Dept Physiol, Sch Med Sci, Fac Med, Sydney, NSW 2052, Australia
[3] Rochester Inst Technol, Int Ctr Hearing & Speech Res, Natl Tech Inst Deaf, Rochester, NY 14623 USA
关键词
Apoptosis; Cochlea; Hearing loss; Gene expression; PCR; Presbycusis;
D O I
10.1007/s10495-008-0266-x
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 understand possible causative roles of apoptosis gene regulation in age-related hearing loss (presbycusis), apoptotic gene expression patterns in the CBA mouse cochlea of four different age and hearing loss groups were compared, using GeneChip and real-time (qPCR) microarrays. GeneChip transcriptional expression patterns of 318 apoptosis-related genes were analyzed. Thirty eight probes (35 genes) showed significant differences in expression. The significant gene families include Caspases, B-cell leukemia/lymphoma2 family, P53, Calpains, Mitogen activated protein kinase family, Jun oncogene, Nuclear factor of kappa light chain gene enhancer in B-cells inhibitor-related and tumor necrosis factor-related genes. The GeneChip results of 31 genes were validated using the new TaqMan (R) Low Density Array (TLDA). Eight genes showed highly correlated results with the GeneChip data. These genes are: activating transcription factor3, B-cell leukemia/lymphoma2, Bcl2-like1, caspase4 apoptosis-related cysteine protease 4, Calpain2, dual specificity phosphatase9, tumor necrosis factor receptor superfamily member12a, and Tumor necrosis factor superfamily member13b, suggesting they may play critical roles in inner ear aging.
引用
收藏
页码:1303 / 1321
页数:19
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