Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Lab Invest. 2010 Oct;90(10):1437-46. doi: 10.1038/labinvest.2010.113. Epub 2010 Jun 14.
The importance of dysregulation of microRNA (miRNA) expression in nonalcoholic steatohepatitis (NASH) has been increasingly recognized; however, the association between altered expression of miRNAs and pathophysiological features of NASH and whether there is a connection between susceptibility to NASH and altered expression of miRNAs are largely unknown. In this study, male inbred C57BL/6J and DBA/2J mice were fed a lipogenic methyl-deficient diet that causes liver injury similar to human NASH, and the expression of miRNAs and the level of proteins targeted by these miRNAs in the livers were determined. Administration of the methyl-deficient diet triggered NASH-specific changes in the livers of C57BL/6J and DBA/2J mice, with the magnitude being more severe in DBA/2J mice. This was evidenced by a greater extent of expression of fibrosis-related genes in the livers of methyl-deficient DBA/2J mice. The development of NASH was accompanied by prominent changes in the expression of miRNAs, including miR-29c, miR-34a, miR-155, and miR-200b. Interestingly, changes in the expression of these miRNAs and protein levels of their targets, including Cebp-β, Socs 1, Zeb-1, and E-cadherin, in the livers of DBA/2J mice fed a methyl-deficient diet were more pronounced as compared with those in C57BL/6J mice. These results show that alterations in the expression of miRNAs are a prominent event during development of NASH induced by methyl deficiency and strongly suggest that severity of NASH and susceptibility to NASH may be determined by variations in miRNA expression response. More important, our data provide a mechanistic link between alterations in miRNA expression and pathophysiological and pathomorphological features of NASH.
非酒精性脂肪性肝炎 (NASH) 中 microRNA (miRNA) 表达失调的重要性已日益受到重视;然而,miRNA 表达的改变与 NASH 的病理生理特征之间的关系以及 NASH 的易感性与 miRNA 表达的改变之间是否存在联系,在很大程度上仍然未知。在这项研究中,雄性近交 C57BL/6J 和 DBA/2J 小鼠喂食一种致肝损伤类似于人类 NASH 的生脂甲基缺陷饮食,测定肝脏中 miRNA 的表达和这些 miRNA 靶向的蛋白质水平。甲基缺陷饮食的给予引发了 C57BL/6J 和 DBA/2J 小鼠肝脏的 NASH 特异性变化,DBA/2J 小鼠的程度更为严重。这从甲基缺陷的 DBA/2J 小鼠肝脏中纤维化相关基因的表达程度更大得到了证明。NASH 的发展伴随着 miRNA 表达的显著变化,包括 miR-29c、miR-34a、miR-155 和 miR-200b。有趣的是,与 C57BL/6J 小鼠相比,喂食甲基缺陷饮食的 DBA/2J 小鼠肝脏中这些 miRNA 的表达变化及其靶蛋白(包括 Cebp-β、SocS1、Zeb-1 和 E-cadherin)的蛋白水平变化更为明显。这些结果表明,miRNA 表达的改变是由甲基缺乏引起的 NASH 发展过程中的一个突出事件,并强烈表明 NASH 的严重程度和对 NASH 的易感性可能由 miRNA 表达反应的变化决定。更重要的是,我们的数据提供了 miRNA 表达改变与 NASH 的病理生理和形态学特征之间的机制联系。