Department of Internal Medicine, Division of Endocrinology, Medical School, University of Patras, Patras, Greece.
PLoS One. 2012;7(4):e34872. doi: 10.1371/journal.pone.0034872. Epub 2012 Apr 4.
Obesity is a major health concern worldwide which is associated with increased risk of chronic diseases such as metabolic syndrome, cardiovascular disease and cancer. The elucidation of the molecular mechanisms involved in adipogenesis and obesogenesis is of essential importance as it could lead to the identification of novel biomarkers and therapeutic targets for the development of anti-obesity drugs. MicroRNAs (miRNAs) have been shown to play regulatory roles in several biological processes. They have become a growing research field and consist of promising pharmaceutical targets in various fields such as cancer, metabolism, etc. The present study investigated the possible implication of miRNAs in adipose tissue during the development of obesity using as a model the C57BLJ6 mice fed a high-fat diet.C57BLJ6 wild type male mice were fed either a standard (SD) or a high-fat diet (HFD) for 5 months. Total RNA was prepared from white adipose tissue and was used for microRNA profiling and qPCR.Twenty-two of the most differentially expressed miRNAs, as identified by the microRNA profiling were validated using qPCR. The results of the present study confirmed previous results. The up-regulation of mmu-miR-222 and the down-regulation of mmu-miR-200b, mmu-miR-200c, mmu-miR-204, mmu-miR-30a*, mmu-miR-193, mmu-miR-378 and mmu-miR-30e* after HFD feeding has also been previously reported. On the other hand, we show for the first time the up-regulation of mmu-miR-342-3p, mmu-miR-142-3p, mmu-miR-142-5p, mmu-miR-21, mmu-miR-146a, mmu-miR-146b, mmu-miR-379 and the down-regulation of mmu-miR-122, mmu-miR-133b, mmu-miR-1, mmu-miR-30a*, mmu-miR-192 and mmu-miR-203 during the development of obesity. However, future studies are warranted in order to understand the exact role that miRNAs play in adipogenesis and obesity.
肥胖是一个全球性的主要健康问题,它与代谢综合征、心血管疾病和癌症等慢性疾病的风险增加有关。阐明脂肪生成和肥胖发生中涉及的分子机制至关重要,因为这可能导致新的生物标志物和治疗靶点的发现,从而开发出抗肥胖药物。微小 RNA(miRNA)已被证明在几种生物过程中发挥调节作用。它们已成为一个不断发展的研究领域,并且在癌症、代谢等各个领域都包含有前途的药物靶点。本研究使用 C57BLJ6 小鼠高脂饮食模型,探讨了 miRNA 在肥胖发生过程中脂肪组织中的可能作用。C57BLJ6 野生型雄性小鼠分别用标准(SD)或高脂饮食(HFD)喂养 5 个月。从白色脂肪组织中提取总 RNA,用于 miRNA 谱分析和 qPCR。通过 miRNA 谱分析鉴定出的 22 个差异表达最多的 miRNA ,用 qPCR 进行验证。本研究的结果证实了之前的结果。HFD 喂养后,mmu-miR-222 的上调和 mmu-miR-200b、mmu-miR-200c、mmu-miR-204、mmu-miR-30a*、mmu-miR-193、mmu-miR-378 和 mmu-miR-30e的下调也有先前报道。另一方面,我们首次显示 mmu-miR-342-3p、mmu-miR-142-3p、mmu-miR-142-5p、mmu-miR-21、mmu-miR-146a、mmu-miR-146b、mmu-miR-379 的上调和 mmu-miR-122、mmu-miR-133b、mmu-miR-1、mmu-miR-30a、mmu-miR-192 和 mmu-miR-203 的下调在肥胖发生过程中。然而,为了了解 miRNA 在脂肪生成和肥胖中的确切作用,还需要进一步的研究。