San Diego State University, San Diego, CA 92182-4614, USA.
Mech Ageing Dev. 2010 Nov-Dec;131(11-12):743-8. doi: 10.1016/j.mad.2010.09.008. Epub 2010 Oct 8.
During adult life, the thymus involutes and thymic output of mature T cells drastically declines. The molecular events underlying this process are not well understood. Here, we present evidence of the importance of miRNAs in regulating T cell differentiation in the aged. miRNAs are a wide-ranging regulatory element influencing gene expression throughout the lifetime of the organism. To establish whether they play a role in the age-specific thymic decline, the miRNA expression pattern was examined in TN subsets of young and aged mice. Fifty-two percent of the miRNAs exhibited elevated expression levels in the aged TN1 cells. This expression profile leads us to hypothesize that the large number of highly expressed miRNAs, indicative of rigidly controlled protein expression, limits the developmental potential of this population and results in the age-induced decline in thymopoiesis.
在成年期,胸腺萎缩,成熟 T 细胞的胸腺输出急剧下降。这一过程的分子事件尚不清楚。在这里,我们提供了 miRNA 在调节老年 T 细胞分化中的重要性的证据。miRNA 是一种广泛存在的调节因子,影响生物体一生中的基因表达。为了确定它们是否在特定于年龄的胸腺衰退中发挥作用,我们检查了年轻和老年小鼠的 TN 亚群中的 miRNA 表达模式。在老年 TN1 细胞中,有 52%的 miRNA 表达水平升高。这种表达谱使我们假设大量高表达的 miRNA,表明严格控制蛋白质表达,限制了该群体的发育潜力,并导致胸腺生成的年龄诱导下降。