Transcriptome analysis of murine thymic epithelial cells reveals age-associated changes in microRNA expression

被引:22
|
作者
Guo, Zhibin [1 ]
Chi, Feng [1 ]
Song, Yan [1 ]
Wang, Changshan [1 ]
Yu, Ruoxing [1 ]
Wei, Tianli [1 ]
Gui, Jingang [2 ]
Zhu, Xike [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Res Ctr, Shenyang 110004, Liaoning, Peoples R China
[2] Geisel Sch Med Dartmouth, Dept Pharmacol & Toxicol, Hanover, NH 03755 USA
关键词
aging; thymic stroma; involution; microRNA; LYMPHOHEMATOPOIETIC PROGENITORS; MIRNA EXPRESSION; WNK1; SCHNURRI-2; KINASE; GENE; MICE; IDENTIFICATION; GENERATION; THYMOCYTE;
D O I
10.3892/ijmm.2013.1471
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Age-related thymic involution is accompanied by a decrease in thymopoiesis and, thus, a deficiency in T cell-mediated immunity in the elderly. A number of events involved in thymic involution have been discovered; however, it remains unclear as to whether they are causes or consequences of thymic involution. These events include the degeneration of T cell progenitors, as well as the deterioration of the thymic stroma, which is a characteristic of thymic epithelial cell loss due to increased apoptosis and decreased cell proliferation. MicroRNAs (miRNAs) are believed to play important roles in the regulation of cell death and proliferation during the aging process. In the present study, we compared the transcriptional levels of various miRNAs in TECs from young and aged mice using microarray analysis. Quantitative PCR was performed to confirm the changes in the expression of miRNAs in the different age groups. Possible downstream targets and pathways of these miRNAs were predicted by performing bioinformatics analysis. To the best of our knowledge, this is the first study to systematically analyze the expression of miRNAs in mouse TECs and to demonstrate that miRNA expression is altered with thymic aging.
引用
收藏
页码:835 / 842
页数:8
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