Department of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
J Cell Physiol. 2013 Jan;228(1):87-98. doi: 10.1002/jcp.24106.
Distal-less homeobox 5 (Dlx5) is a positive regulator of osteoblast differentiation that contains a homeobox domain. Because there are possible reciprocal relationships between osteogenic and adipogenic differentiation of bone marrow mesenchymal stem cells (MSCs), we examined the regulatory role of Dlx5 in adipogenic differentiation in this study. Adipogenic stimuli suppressed the expression levels of Dlx5 mRNA in mouse bone marrow stromal cells. Over-expression of Dlx5 inhibited adipogenic differentiation in human bone marrow MSCs and 3T3-L1 preadipocytic cells whereas knockdown of Dlx5 enhanced adipogenic differentiation in 3T3-L1 cells. Over-expression of Dlx5 suppressed the expression of adipogenic marker genes, including CCAAT/enhancer-binding protein α (C/EBPα) and peroxisome proliferator-activated receptor γ (PPARγ). Dlx5-mediated suppression of adipogenic differentiation was overcome by over-expression of PPARγ but not by that of cAMP response element binding protein (CREB) or C/EBPα. Dlx5 decreased the transcriptional activity of CREB and C/EBPα in a dose-dependent manner. Dlx5 directly bound to CREB and C/EBPα and prevented them from binding to and subsequently transactivating the PPARγ promoter. These results suggest that Dlx5 plays an important regulatory role in fate determination of bone marrow MSCs toward the osteoblast lineage through the inhibition of adipocyte differentiation as well as the direct stimulation of osteoblast differentiation.
远端同源盒 5(Dlx5)是成骨细胞分化的正调控因子,它含有一个同源盒结构域。由于骨髓间充质干细胞(MSCs)的成骨和脂肪分化之间可能存在相互关系,我们在这项研究中检查了 Dlx5 在脂肪分化中的调节作用。脂肪分化刺激物抑制了小鼠骨髓基质细胞中 Dlx5 mRNA 的表达水平。Dlx5 的过表达抑制了人骨髓 MSCs 和 3T3-L1 前脂肪细胞的脂肪分化,而 Dlx5 的敲低则增强了 3T3-L1 细胞的脂肪分化。Dlx5 的过表达抑制了脂肪生成标记基因的表达,包括 CCAAT/增强子结合蛋白α(C/EBPα)和过氧化物酶体增殖物激活受体γ(PPARγ)。过表达 PPARγ可以克服 Dlx5 介导的脂肪生成分化抑制,但不能克服 cAMP 反应元件结合蛋白(CREB)或 C/EBPα的过表达。Dlx5 以剂量依赖的方式降低了 CREB 和 C/EBPα 的转录活性。Dlx5 直接与 CREB 和 C/EBPα结合,并阻止它们结合并随后激活 PPARγ 启动子。这些结果表明,Dlx5 通过抑制脂肪细胞分化以及直接刺激成骨细胞分化,在骨髓 MSCs 向成骨细胞谱系的命运决定中发挥重要的调节作用。