Department of Orthopaedic Surgery, Yonsei University College of Medicine, Seoul, South Korea.
Stem Cells Dev. 2012 Dec 10;21(18):3298-308. doi: 10.1089/scd.2011.0732. Epub 2012 Aug 10.
microRNAs are small molecules, about 17-23 nucleotides in length, that act as translational regulators of their target gene. By binding to a target, microRNAs are known to either inhibit translation or induce degradation of the target. Despite the great interest in microRNAs, however, the exact targets of each individual microRNA in different processes remain largely unknown. In this study, we determined that the lymphoid enhancer-binding factor-1 (LEF-1) was expressed during the chondrogenesis of human bone marrow-derived mesenchymal stem cells (hBM-MSCs) and sought to identify a novel microRNA targeting this gene. Through subsequent studies, we have identified, for the first time, one particular microRNA, miR-449a, that recognizes and regulates the expression of LEF-1 in a dose-dependent and sequence-specific manner. In addition, we observed that the inhibition of LEF-1 via miR-449a led to the subsequent repression of Sox 9, which is a well-established regulator of chondrogenesis. Collectively, this study demonstrated that miR-449a directly targets LEF-1, which in turn affects the expression of Sox 9, ultimately leading to the proper regulation of the differentiation and chondrogenesis of human MSCs (hBM-MSCs).
微小 RNA 是一种小分子,长度约为 17-23 个核苷酸,作为其靶基因的翻译调节剂。通过与靶标结合,微小 RNA 已知可以抑制翻译或诱导靶标的降解。然而,尽管人们对微小 RNA 非常感兴趣,但不同过程中每个微小 RNA 的确切靶标在很大程度上仍然未知。在这项研究中,我们确定淋巴增强结合因子 1(LEF-1)在人骨髓间充质干细胞(hBM-MSCs)的软骨生成过程中表达,并试图鉴定靶向该基因的新型微小 RNA。通过随后的研究,我们首次鉴定出一种特定的微小 RNA,miR-449a,它以剂量依赖和序列特异性的方式识别并调节 LEF-1 的表达。此外,我们观察到通过 miR-449a 抑制 LEF-1 会导致 Sox9 的随后抑制,Sox9 是软骨生成的公认调节剂。总的来说,这项研究表明 miR-449a 直接靶向 LEF-1,进而影响 Sox9 的表达,最终导致人 MSCs(hBM-MSCs)的分化和软骨生成的适当调节。