Genes involved in immunity and apoptosis are associated with human presbycusis based on microarray analysis
Genes involved in immunity and apoptosis are associated with human presbycusis based on microarray analysis
复制标题
基于微阵列分析,涉及免疫和细胞凋亡的基因与人类老年性耳聋相关
DOI:
10.3109/00016489.2014.880795
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发表时间:
2014-06-01
影响因子:
1.4
通讯作者:
Shi, Jianrong
中科院分区:
文献类型:
--
作者:
Dong, Yang;Li, Ming;Shi, Jianrong
Abstract Conclusions: Genes involved in immunity and apoptosis were associated with human presbycusis. CCR3 and GILZ played an important role in the pathogenesis of presbycusis, probably through regulating chemokine receptor, T-cell apoptosis, or T-cell activation pathways. Objectives: To identify genes associated with human presbycusis and explore the molecular mechanism of presbycusis. Methods: Hearing function was tested by pure-tone audiometry. Microarray analysis was performed to identify presbycusis-correlated genes by Illumina Human-6 BeadChip using the peripheral blood samples of subjects. To identify biological process categories and pathways associated with presbycusis-correlated genes, bioinformatics analysis was carried out by Gene Ontology Tree Machine (GOTM) and database for annotation, visualization, and integrated discovery (DAVID). Quantitative RT-PCR (qRT-PCR) was used to validate the microarray data. Results: Microarray analysis identified 469 up-regulated genes and 323 down-regulated genes. Both the dominant biological processes by Gene Ontology (GO) analysis and the enriched pathways by Kyoto encyclopedia of genes and genomes (KEGG) and BIOCARTA showed that genes involved in immunity and apoptosis were associated with presbycusis. In addition, CCR3, GILZ, CXCL10, and CX3CR1 genes showed consistent difference between groups for both the gene chip and qRT-PCR data. The differences of CCR3 and GILZ between presbycusis patients and controls were statistically significant (p < 0.05).