Laboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Cell Biol Int. 2013 Sep;37(9):905-16. doi: 10.1002/cbin.10115. Epub 2013 May 7.
FoxO1 and C/EBPβ are important transcription factors during adipogenic differentiation; however, the potential mechanisms of their inter-regulation in adipogenesis remain unknown. We found that FoxO1 and C/EBPβ are abundant in adipose tissues of 3- and 180-day pigs at the mRNA and protein levels. During porcine preadipocyte differentiation, C/EBPβ expression increases to the peak at Day 2 and then decreases. In contrast, FoxO1 is lowest on Day 2 and gradually increases. Knockdown of FoxO1 or C/EBPβ with lentivirus-mediated shRNA enhances or inhibits lipid accumulation and adipogenic maker (C/EBPα and aP2) expression, respectively. FoxO1 depletion causes a mild decrease of C/EBPβ protein level, and C/EBPβ interference also inhibits the expression of FoxO1 protein. Knockdown of both FoxO1 and C/EBPβ promotes lipid accumulation at Day 8, and increases the adipogenic markers during differentiation in comparison with the controls and the FoxO1 knockdown alone. Co-immunoprecipitation experiments indicate that FoxO1 binds to C/EBPβ in adipose tissues and in vitro. In conclusion, the results suggest that FoxO1 and C/EBPβ regulate preadipocyte adipogenesis possibly through C/EBPβ → FoxO1 → C/EBPβ feedback regulatory loop and FoxO1-C/EBPβ protein complex.
FoxO1 和 C/EBPβ 是脂肪生成分化过程中的重要转录因子;然而,它们在脂肪生成中的相互调控的潜在机制尚不清楚。我们发现 FoxO1 和 C/EBPβ 在 3 天和 180 天猪的脂肪组织中在 mRNA 和蛋白水平上都很丰富。在猪前体脂肪细胞分化过程中,C/EBPβ 的表达在第 2 天达到高峰,然后下降。相比之下,FoxO1 在第 2 天最低,然后逐渐增加。用慢病毒介导的 shRNA 敲低 FoxO1 或 C/EBPβ 分别增强或抑制脂质积累和脂肪生成标志物(C/EBPα 和 aP2)的表达。FoxO1 的耗竭导致 C/EBPβ 蛋白水平的轻微下降,而 C/EBPβ 的干扰也抑制了 FoxO1 蛋白的表达。与对照组和单独敲低 FoxO1 相比,同时敲低 FoxO1 和 C/EBPβ 可促进第 8 天的脂质积累,并在分化过程中增加脂肪生成标志物。共免疫沉淀实验表明 FoxO1 在脂肪组织中和体外与 C/EBPβ 结合。总之,这些结果表明 FoxO1 和 C/EBPβ 可能通过 C/EBPβ→FoxO1→C/EBPβ 反馈调节环和 FoxO1-C/EBPβ 蛋白复合物来调节前体脂肪细胞的脂肪生成。