Matsubara Yoshiyuki, Endo Tsuyoshi, Kano Koichiro
Laboratory of Cell and Tissue Biology, Graduate School of Bioresource Sciences, Nihon University, Kanagawa, Japan.
Comp Biochem Physiol A Mol Integr Physiol. 2008 Dec;151(4):511-8. doi: 10.1016/j.cbpa.2008.07.002. Epub 2008 Jul 6.
The present study was carried out to clarify the direct effect of fatty acids (FAs) on chick (Gallus gallus) adipocyte differentiation in the absence of dexmethasone (DEX), a commonly used as strong inducer for adipocyte differentiation. Adipocyte differentiation was initiated by maintaining confluent cell in serum-free medium supplemented with FAs. Upon exposure to FAs, glycerol-3-phosphate dehydrogenase activity (GPDH) as adipocyte differentiation marker rapidly increased, and was significantly higher in chick adipocyte than in control cell. The morphology of the FAs-treated cell changed from fibroblast-like to polygon, and the cells accumulated many cytoplasmic lipid droplets as estimated by Oil red O staining. Neither insulin nor bovine serum albumin, as substitutes for serum, had an effect on chick adipocyte differentiation. The FAs-treated cell had a higher protein and mRNA expression levels for peroxisome proliferator-activated receptor-gamma (PPARgamma), a master regulator of differentiation, compared with untreated cell. In FAs-treated cell, the mRNA expression levels of adipocyte-specific genes, such as CCAAT/enhancer binding protein-alpha (C/EBP alpha) and adipocyte fatty acid-binding protein (aP2) were higher than in control cell. These results indicated that FAs, but not DEX, are essential inducers for chick adipocyte differentiation by elevating PPARgamma expression.
本研究旨在阐明在没有地塞米松(DEX)的情况下脂肪酸(FAs)对雏鸡(原鸡)脂肪细胞分化的直接影响,地塞米松是一种常用的强效脂肪细胞分化诱导剂。通过在补充了FAs的无血清培养基中维持汇合细胞来启动脂肪细胞分化。暴露于FAs后,作为脂肪细胞分化标志物的甘油-3-磷酸脱氢酶活性(GPDH)迅速增加,并且在雏鸡脂肪细胞中显著高于对照细胞。经FAs处理的细胞形态从成纤维细胞样变为多边形,并且通过油红O染色估计细胞积累了许多细胞质脂滴。胰岛素和牛血清白蛋白作为血清替代品,对雏鸡脂肪细胞分化均无影响。与未处理的细胞相比,经FAs处理的细胞中过氧化物酶体增殖物激活受体γ(PPARγ)(一种分化的主要调节因子)的蛋白质和mRNA表达水平更高。在经FAs处理的细胞中,脂肪细胞特异性基因如CCAAT/增强子结合蛋白α(C/EBPα)和脂肪细胞脂肪酸结合蛋白(aP2)的mRNA表达水平高于对照细胞。这些结果表明,FAs而非DEX是通过提高PPARγ表达来诱导雏鸡脂肪细胞分化的必需诱导剂。