Research Center, Shengjing Hospital, China Medical University, Shenyang, Liaoning 110004, PR China.
Int J Mol Med. 2013 Oct;32(4):835-42. doi: 10.3892/ijmm.2013.1471. Epub 2013 Aug 21.
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.
衰老是与年龄相关的,与胸腺细胞生成减少相关的,因而与老年人的 T 细胞介导的免疫功能下降相关。有许多与胸腺萎缩相关的事件已经被发现,然而,它们究竟是胸腺萎缩的原因还是结果还不清楚。这些事件包括 T 细胞祖细胞的退化,以及胸腺基质的恶化,这是由于胸腺上皮细胞凋亡增加和细胞增殖减少导致的特征性变化。microRNAs(miRNAs)被认为在衰老过程中细胞死亡和增殖的调控中发挥重要作用。在本研究中,我们使用微阵列分析比较了来自年轻和老年小鼠的 TECs 中的各种 miRNAs 的转录水平。通过定量 PCR 验证了不同年龄组中 miRNA 表达的变化。通过进行生物信息学分析预测了这些 miRNAs 的可能下游靶标和途径。据我们所知,这是第一项系统性地分析小鼠 TECs 中 miRNAs 表达的研究,并证明了 miRNA 表达随着胸腺衰老而改变。