Qin Yu, Zhao Jiangyue, Min Xiaojie, Wang Mingwu, Luo Wenting, Wu Di, Yan Qichang, Li Jing, Wu Xinwei, Zhang Jinsong
Biochim Biophys Acta. 2014 Dec;1842(12 Pt A):2439-47. doi: 10.1016/j.bbadis.2014.10.002.
MicroRNA-125b (miR-125b) has been implicated in a variety of diseases as either repressors or promoters, and plays crucial roles in many cellular processes such as cell differentiation, proliferation and apoptosis. Age-related cataract has become one of the most serious problems facing the aging population in the world. The purpose of this study was to investigate the role of miR-125b in the development of age-related cataract. We demonstrated that miR-125b was downregulated in both age-related cataract tissue and lens epithelial cell apoptosis induced by UV irradiation. We also identified the impact of miR-125b on apoptosis in a lens epithelial cell line. In vitro, miR-125b regulates human lens epithelial cell apoptosis at least in part by directly targeting p53. In addition,an inverse relationship between miR-125b and p53 expression was seen in age-related cataract tissue. In conclusion,this study suggests that miR-125b might be closely involved in the pathogenesis of cataract, and has the potential to be a diagnostic biomarker or even a therapeutic modality for cataract.
微小RNA-125b(miR-125b)在多种疾病中既作为抑制因子又作为促进因子发挥作用,并且在许多细胞过程如细胞分化、增殖和凋亡中起关键作用。年龄相关性白内障已成为世界老龄人口面临的最严重问题之一。本研究的目的是探讨miR-125b在年龄相关性白内障发生发展中的作用。我们证明,miR-125b在年龄相关性白内障组织和紫外线照射诱导的晶状体上皮细胞凋亡中均下调。我们还确定了miR-125b对晶状体上皮细胞系凋亡的影响。在体外,miR-125b至少部分通过直接靶向p53来调节人晶状体上皮细胞凋亡。此外,在年龄相关性白内障组织中观察到miR-125b与p53表达之间呈负相关。总之,本研究表明miR-125b可能密切参与白内障的发病机制,并且有可能成为白内障的诊断生物标志物甚至治疗手段。