Laboratory of Biodefense and Regulation, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka, Japan.
Gene. 2011 Mar 1;473(2):150-6. doi: 10.1016/j.gene.2010.12.002. Epub 2010 Dec 15.
Forkhead/winged helix transcription factors (Foxs) regulate differentiation, metabolism, and development. Although Foxa1 is expressed in adipocytes, the roles and regulation of Foxa1 in them remain unclear. Here, we found that under the control of C/EBPβ, Foxa1 suppressed lipid accumulation and concomitantly caused a decrease in adipogenic gene expression in adipocytes. Foxa1 was expressed in undifferentiated mouse 3T3-L1 cells and in the early phase of adipogenesis, with its highest expression at 3h after the initiation of adipogenesis, which was followed by a subsequent decrease. SiRNA-mediated suppression of Foxa1 expression activated the expression of adipogenic genes such as PPARγ. Moreover, siRNAs for C/EBPβ, but not those for C/EBPδ, reduced Foxa1 mRNA and protein levels. The results of a promoter-reporter assay and chromatin immunoprecipitation assay demonstrated that C/EBPβ bound to the C/EBP binding element at -529 of the mouse Foxa1 promoter. Furthermore, siRNA-mediated knockdown of C/EBPβ decreased the promoter activity of mouse Foxa1 gene. These results suggest that Foxa1 plays a suppressive role in the early phase of adipogenesis, acting under the control of C/EBPβ, and might be involved in the regulation of the rate of progression of the early phase of adipogenesis.
叉头/翼状螺旋转录因子(Foxs)调节分化、代谢和发育。虽然 Foxa1 在脂肪细胞中表达,但它在其中的作用和调节仍不清楚。在这里,我们发现 Foxa1 在 C/EBPβ的控制下抑制脂肪积累,同时导致脂肪细胞中成脂基因表达的降低。Foxa1 在未分化的小鼠 3T3-L1 细胞和脂肪生成的早期阶段表达,在脂肪生成开始后 3 小时表达最高,随后表达下降。Foxa1 表达的 siRNA 抑制激活了 PPARγ等成脂基因的表达。此外,C/EBPβ的 siRNA,但不是 C/EBPδ的 siRNA,降低了 Foxa1 mRNA 和蛋白水平。启动子报告基因检测和染色质免疫沉淀检测的结果表明,C/EBPβ结合到 Foxa1 启动子-529 处的 C/EBP 结合元件。此外,C/EBPβ 的 siRNA 介导的敲低降低了小鼠 Foxa1 基因的启动子活性。这些结果表明,Foxa1 在脂肪生成的早期阶段发挥抑制作用,受 C/EBPβ的控制,可能参与调节早期脂肪生成阶段的进展速度。