Padgett Kerstien A, Lan Ruth Y, Leung Patrick C, Lleo Ana, Dawson Kevin, Pfeiff Janice, Mao Tin K, Coppel Ross L, Ansari Aftab A, Gershwin M Eric
Department of Medical Microbiology and Immunology, University of California, Davis, CA 95616, USA.
J Autoimmun. 2009 May-Jun;32(3-4):246-53. doi: 10.1016/j.jaut.2009.02.022. Epub 2009 Apr 3.
MicroRNAs (miRNAs) are small RNA molecules that negatively regulate protein coding gene expression and are thought to play a critical role in many biological processes. Aberrant levels of miRNAs have been associated with numerous diseases and cancers, and as such, miRNAs have gain much interests as diagnostic biomarkers, and as therapeutic targets. However, their role in autoimmunity is largely unknown. The aims of this study are to: (1) identify differentially expressed miRNAs in human primary biliary cirrhosis (PBC); (2) validate these independently; and (3) identify potential targets of differentially expressed miRNAs. We compared the expression of 377 miRNAs in explanted livers form subjects with PBC versus controls with normal liver histology. A total of 35 independent miRNAs were found to be differentially expressed in PBC (p < 0.001). Quantitative PCR was employed to validate down-regulation of microRNA-122a (miR-122a) and miR-26a and the increased expression of miR-328 and miR-299-5p. The predicted targets of these miRNAs are known to affect cell proliferation, apoptosis, inflammation, oxidative stress, and metabolism. Our data are the first to demonstrate that PBC is characterized by altered expression of hepatic miRNA; however additional studies are required to demonstrate a causal link between those miRNA and the development of PBC.
微小RNA(miRNA)是一类小RNA分子,它们负向调节蛋白质编码基因的表达,并被认为在许多生物学过程中发挥关键作用。miRNA水平异常与多种疾病和癌症相关,因此,miRNA作为诊断生物标志物和治疗靶点备受关注。然而,它们在自身免疫中的作用在很大程度上尚不清楚。本研究的目的是:(1)鉴定人类原发性胆汁性肝硬化(PBC)中差异表达的miRNA;(2)独立验证这些miRNA;(3)鉴定差异表达miRNA的潜在靶标。我们比较了PBC患者与肝组织学正常的对照者的移植肝中377种miRNA的表达。共发现35种独立的miRNA在PBC中差异表达(p < 0.001)。采用定量PCR验证微小RNA-122a(miR-122a)和miR-26a的下调以及miR-328和miR-299-5p的表达增加。已知这些miRNA的预测靶标会影响细胞增殖、凋亡、炎症、氧化应激和代谢。我们的数据首次证明PBC的特征是肝脏miRNA表达改变;然而,需要进一步的研究来证明这些miRNA与PBC发生之间的因果关系。