Adachi H, Kurachi H, Homma H, Adachi K, Imai T, Morishige K, Matsuzawa Y, Miyake A
Department of Obstetrics and Gynecology, Osaka University Medical School, Japan.
Endocrinology. 1994 Nov;135(5):1824-30. doi: 10.1210/endo.135.5.7956906.
We have reported the importance of epidermal growth factor (EGF) for the induction of obesity in mice. In this study, we studied the effects of EGF on the induction of lipogenic enzymes and on the accumulation of triglyceride in a differentiated mouse adipocyte cell in vitro. Mouse 3T3-L1 preadipocytic cells differentiated into mature adipocytes after the differentiation procedure by insulin, dexamethasone, and methyl-isobutyl-xanthine. 125I-EGF binding studies in the differentiated 3T3-L1 cells showed specific 125I-EGF bindings, and they expressed gene transcripts for EGF receptors by reverse transcription and polymerase chain reaction at all differentiative stages examined. Although EGF showed inhibitory effects on the triglyceride accumulation when administered to the preadipocytic 3T3-L1 cells, EGF enhanced the adipogenesis in the differentiated cells in dose- and time-dependent manners. Administration of EGF at 0.1-1 nM from 4 days after the differentiation procedure for 10 days, significantly enhanced the acyl-Co A synthetase and lipoprotein lipase messenger RNA levels, both of which are rate-limiting enzymes to synthesize triglyceride in adipocytes. Moreover, 0.1-1 nM EGF increased the amounts of triglyceride accumulated in the cells, in proportion to the acyl-Co A synthetase and lipoprotein lipase messenger RNA levels. EGF rather failed the adipogenesis at 10 nM. Time course studies revealed that 1 nM EGF significantly increased the intracellular triglyceride levels from 4 through 16 days administration. These results suggest that EGF shows biphasic effects on adipocytes: although EGF inhibits preadipocytes differentiation into mature adipocytes, it promotes adipogenesis in the differentiated adipocytes.
我们已经报道了表皮生长因子(EGF)在诱导小鼠肥胖中的重要性。在本研究中,我们在体外研究了EGF对分化的小鼠脂肪细胞中脂肪生成酶的诱导作用以及甘油三酯积累的影响。小鼠3T3-L1前脂肪细胞在经过胰岛素、地塞米松和甲基异丁基黄嘌呤的分化程序后分化为成熟脂肪细胞。在分化的3T3-L1细胞中进行的125I-EGF结合研究显示有特异性的125I-EGF结合,并且在所有检测的分化阶段,它们通过逆转录和聚合酶链反应表达EGF受体的基因转录本。尽管将EGF施用于前脂肪细胞3T3-L1时对甘油三酯积累显示出抑制作用,但EGF以剂量和时间依赖性方式增强了分化细胞中的脂肪生成。在分化程序后4天开始给予0.1 - 1 nM的EGF并持续10天,显著提高了酰基辅酶A合成酶和脂蛋白脂肪酶信使RNA水平,这两种酶都是脂肪细胞中合成甘油三酯的限速酶。此外,0.1 - 1 nM的EGF增加了细胞内积累的甘油三酯量,与酰基辅酶A合成酶和脂蛋白脂肪酶信使RNA水平成比例。而10 nM的EGF则抑制了脂肪生成。时间进程研究表明,1 nM的EGF在给药4至16天期间显著增加了细胞内甘油三酯水平。这些结果表明,EGF对脂肪细胞具有双相作用:尽管EGF抑制前脂肪细胞分化为成熟脂肪细胞,但它促进分化脂肪细胞中的脂肪生成。