Department of Biochemistry, Centro de Investigación y de Estudios Avanzados del Instituto Politcénico Nacional, Mexico City, Federal District, 07360, Mexico.
Sci Rep. 2011;1:178. doi: 10.1038/srep00178. Epub 2011 Dec 1.
Adipogenesis is regulated by a complex cascade of transcriptional factors, but little is known about the early events that regulate the adipogenic program. Here, we report the role of the srebf1a gene in the differentiation of fibroblastic 3T3-F442A cells. We found that expression of srebf1a depended on GSK3β activity and that GSK3β activity was necessary for C/EBPβ phosphorylation at Thr188. Knockdown of srebf1a inhibited the adipogenic program because it blocked the expression of genes encoding PPARγ2, C/EBPα, SREBP1c and even FABP4, demonstrating that SREBP1a activation is upstream of these three essential adipogenic transcription factors. Kinetic analysis during differentiation illustrated that the order of expression of adipogenic genes was the following: cebpb, srebf1a, pparg2, cebpa, srebp1c and fabp4. Our data suggest that srebf1a acts as an essential link between the GSK3β-C/EBPβ signaling axis and the beginning of the adipogenic transcriptional cascade.
脂肪生成受转录因子的复杂级联调控,但对于调节脂肪生成程序的早期事件知之甚少。在这里,我们报告了 srebf1a 基因在成纤维细胞 3T3-F442A 细胞分化中的作用。我们发现 srebf1a 的表达依赖于 GSK3β 的活性,而 GSK3β 的活性对于 C/EBPβ 在 Thr188 处的磷酸化是必需的。srebf1a 的敲低抑制了脂肪生成程序,因为它阻断了编码 PPARγ2、C/EBPα、SREBP1c 甚至 FABP4 的基因的表达,表明 SREBP1a 的激活位于这三个必需的脂肪生成转录因子的上游。分化过程中的动力学分析表明,脂肪生成基因的表达顺序如下:cebpb、srebf1a、pparg2、cebpa、srebp1c 和 fabp4。我们的数据表明 srebf1a 作为 GSK3β-C/EBPβ 信号轴与脂肪生成转录级联开始之间的重要联系。