Suppr超能文献

肝 microRNAs miR-29c、miR-34a、miR-155 和 miR-200b 的表达差异与小鼠对饮食性非酒精性脂肪性肝炎的种属特异性易感性相关。

Difference in expression of hepatic microRNAs miR-29c, miR-34a, miR-155, and miR-200b is associated with strain-specific susceptibility to dietary nonalcoholic steatohepatitis in mice.

机构信息

Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.

出版信息

Lab Invest. 2010 Oct;90(10):1437-46. doi: 10.1038/labinvest.2010.113. Epub 2010 Jun 14.

Abstract

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.

摘要

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。

相似文献

引用本文的文献

3
The contribution of genetics and epigenetics to MAFLD susceptibility.遗传学和表观遗传学对 MAFLD 易感性的贡献。
Hepatol Int. 2024 Oct;18(Suppl 2):848-860. doi: 10.1007/s12072-024-10667-5. Epub 2024 Apr 25.
10
Therapeutic molecular targets of SSc-ILD.系统性硬化症相关间质性肺疾病的治疗分子靶点。
J Scleroderma Relat Disord. 2020 Mar;5(2 Suppl):17-30. doi: 10.1177/2397198319899013. Epub 2020 Jan 22.

本文引用的文献

4
Meta-regulation: microRNA regulation of glucose and lipid metabolism.元调控:miRNA 对葡萄糖和脂代谢的调控。
Trends Endocrinol Metab. 2009 Nov;20(9):452-9. doi: 10.1016/j.tem.2009.05.007. Epub 2009 Sep 30.
10
Diet-induced hepatocellular carcinoma in genetically predisposed mice.基因易感性小鼠中饮食诱导的肝细胞癌
Hum Mol Genet. 2009 Aug 15;18(16):2975-88. doi: 10.1093/hmg/ddp236. Epub 2009 May 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验