Noren Hooten Nicole, Fitzpatrick Megan, Wood William H, De Supriyo, Ejiogu Ngozi, Zhang Yongqing, Mattison Julie A, Becker Kevin G, Zonderman Alan B, Evans Michele K
Laboratory of Epidemiology and Population Sciences, National Institutes of Health, Baltimore, MD 21224, USA.
Aging (Albany NY). 2013 Oct;5(10):725-40. doi: 10.18632/aging.100603.
MicroRNAs (miRNAs) are small noncoding RNAs that post-transcriptionally regulate gene expression by targeting specific mRNAs. Altered expression of circulating miRNAs have been associated with age-related diseases including cancer and cardiovascular disease. Although we and others have found an age-dependent decrease in miRNA expression in peripheral blood mononuclear cells (PBMCs), little is known about the role of circulating miRNAs in human aging. Here, we examined miRNA expression in human serum from young (mean age 30 years) and old (mean age 64 years) individuals using next generation sequencing technology and real-time quantitative PCR. Of the miRNAs that we found to be present in serum, three were significantly decreased in 20 older individuals compared to 20 younger individuals: miR-151a-5p, miR-181a-5p and miR-1248. Consistent with our data in humans, these miRNAs are also present at lower levels in the serum of elderly rhesus monkeys. In humans, miR-1248 was found to regulate the expression of mRNAs involved in inflammatory pathways and miR-181a was found to correlate negatively with the pro-inflammatory cytokines IL-6 and TNFα and to correlate positively with the anti-inflammatory cytokines TGFβ and IL-10. These results suggest that circulating miRNAs may be a biological marker of aging and could also be important for regulating longevity. Identification of stable miRNA biomarkers in serum could have great potential as a noninvasive diagnostic tool as well as enhance our understanding of physiological changes that occur with age.
微小RNA(miRNA)是一类小的非编码RNA,通过靶向特定的信使核糖核酸(mRNA)在转录后水平调控基因表达。循环miRNA表达的改变与包括癌症和心血管疾病在内的与年龄相关的疾病有关。尽管我们和其他人已经发现外周血单核细胞(PBMC)中miRNA表达存在年龄依赖性下降,但关于循环miRNA在人类衰老中的作用知之甚少。在这里,我们使用下一代测序技术和实时定量聚合酶链反应检测了年轻(平均年龄30岁)和年老(平均年龄64岁)个体血清中的miRNA表达。在我们发现存在于血清中的miRNA中,与20名年轻个体相比,20名年老个体中有三种显著下降:miR-151a-5p、miR-181a-5p和miR-1248。与我们在人类中的数据一致,这些miRNA在老年恒河猴血清中的水平也较低。在人类中,发现miR-1248调节参与炎症途径的mRNA表达,并且发现miR-181a与促炎细胞因子白细胞介素-6(IL-6)和肿瘤坏死因子α(TNFα)呈负相关,与抗炎细胞因子转化生长因子β(TGFβ)和白细胞介素-10(IL-10)呈正相关。这些结果表明,循环miRNA可能是衰老的生物学标志物,对调节寿命也可能很重要。血清中稳定的miRNA生物标志物的鉴定作为一种非侵入性诊断工具可能具有巨大潜力,同时也能增强我们对随年龄发生的生理变化的理解。