Bae Eun Ju, Kim Sang Geon
College of Pharmacy, Seoul National University, Sillim-dong, Kwanak-gu, Seoul 151-742, South Korea.
Mol Pharmacol. 2005 Sep;68(3):660-9. doi: 10.1124/mol.105.012997. Epub 2005 Jun 16.
The CCAAT/enhancer-binding protein (C/EBP) beta-isoforms liver-enriched activator protein (LAP) and truncated dominant-negative liver-enriched inhibitory protein (LIP) differentially regulate adipogenesis. We previously demonstrated that oltipraz (5-[2-pyrazinyl]-4-methyl-1,2-dithiol-3-thione), a cancer-chemopreventive agent, promotes C/EBPbeta-LAP activation in hepatocytes. This study investigated whether oltipraz affects adipocyte differentiation and, if so, the molecular basis for the alterations in adipogenesis. The expression of LIP notably increased 6 to 48 h after oltipraz treatment of 3T3-L1 preadipocytes, whereas that of LAP was minimally changed. Oltipraz treatment approximately 3-fold elevated the ratio of LIP to LAP. Immunoblot, gel-shift, and Southwestern analyses revealed that oltipraz enhanced the levels of nuclear LIP and LAP and their binding to the C/EBP-binding site. Cotransfection of predipocytes with the plasmid encoding LIP interfered with LAP-mediated luciferase expression, confirming the inhibitory role of LIP in gene expression. Likewise, LAP-mediated luciferase gene transactivation was inhibited by oltipraz, as was observed by cotransfection of a dominant-negative mutant form of C/EBP. Oltipraz enhanced cytoplasmic translocation and RNA binding of CUG repeat-binding protein-1 (CUGBP1) but not calreticulin, another RNA-binding protein that interacts with C/EBPbeta mRNA. When 3T3-L1 preadipocytes were induced to differentiate by exposure to 3-isobutyl-1-methylxanthine, dexamethasone, and insulin, oltipraz markedly inhibited hormone-induced adipocyte differentiation. In primary cultured rat preadipocytes, oltipraz enhanced LIP production and inhibited adipocyte differentiation. In conclusion, oltipraz inhibits adipogenesis by promoting LIP production and activation, and the enhanced LIP production accompanies cytoplasmic translocation of CUGBP1 and its binding to the GC-rich region of C/EBPbeta mRNA. Our finding holds significance in that adipogenesis can be pharmacologically controlled by LIP production.
CCAAT/增强子结合蛋白(C/EBP)β异构体肝脏富集激活蛋白(LAP)和截短的显性负性肝脏富集抑制蛋白(LIP)对脂肪生成具有不同的调节作用。我们之前证明,癌症化学预防剂奥替普拉(5-[2-吡嗪基]-4-甲基-1,2-二硫醇-3-硫酮)可促进肝细胞中C/EBPβ-LAP的激活。本研究调查了奥替普拉是否影响脂肪细胞分化,若有影响,其影响脂肪生成改变的分子基础是什么。在对3T3-L1前脂肪细胞进行奥替普拉处理后6至48小时,LIP的表达显著增加,而LAP的表达变化极小。奥替普拉处理使LIP与LAP的比例升高了约3倍。免疫印迹、凝胶迁移和蛋白质印迹分析表明,奥替普拉提高了核LIP和LAP的水平及其与C/EBP结合位点的结合。用编码LIP的质粒对前脂肪细胞进行共转染会干扰LAP介导的荧光素酶表达,证实了LIP在基因表达中的抑制作用。同样,奥替普拉抑制了LAP介导的荧光素酶基因反式激活,这与共转染C/EBP的显性负性突变体形式时观察到的情况相同。奥替普拉增强了CUG重复结合蛋白1(CUGBP1)的细胞质易位和RNA结合,但未增强钙网蛋白(另一种与C/EBPβmRNA相互作用的RNA结合蛋白)的细胞质易位和RNA结合。当3T3-L1前脂肪细胞通过暴露于3-异丁基-1-甲基黄嘌呤、地塞米松和胰岛素而被诱导分化时,奥替普拉显著抑制激素诱导的脂肪细胞分化。在原代培养的大鼠前脂肪细胞中,奥替普拉增强了LIP的产生并抑制了脂肪细胞分化。总之,奥替普拉通过促进LIP的产生和激活来抑制脂肪生成,而LIP产生的增加伴随着CUGBP1的细胞质易位及其与C/EBPβmRNA富含GC区域的结合。我们的发现具有重要意义,即脂肪生成可以通过控制LIP的产生进行药理学调控。