首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >RAPAMYCIN INHIBITS CLONAL EXPANSION AND ADIPOGENIC DIFFERENTIATION OF 3T3-L1 CELLS
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RAPAMYCIN INHIBITS CLONAL EXPANSION AND ADIPOGENIC DIFFERENTIATION OF 3T3-L1 CELLS

机译:雷帕霉素可抑制3T3-L1细胞的克隆扩增和成脂分化

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摘要

The temporal expression profile of this protein, designated FK506-binding protein (FKBP) 51, is concordant with the clonal-expansion period undertaken by 3T3-L1 cells after exposure to adipogenic hormones, Having observed FKBP51 synthesis early during adipogenesis, we tested the effects of three immunosuppressive drugs-cyclosporin A, FK506, and rapamycin-on the terminal-differentiation process. Adipocyte conversion was not affected by either cyclosporin A or FK506 and yet was significantly reduced by rapamycin at drug concentrations as low as 10 nM. Clonal expansion was impeded in drug-treated cultures, as was the accumulation of cytoplasmic lipid droplets normally seen late during differentiation. Rapamycin treatment likewise inhibited the expression of CCAAT/enhancer binding protein alpha a transcription factor required for 3T3-L1 cell differentiation. All three of these effects were reversed by high FK506 concentrations, indicating that the operative inhibitory event was mediated by an immunophilin-rapamycin complex. [References: 46]
机译:该蛋白的时间表达谱称为FK506结合蛋白(FKBP)51,与暴露于成脂激素后3T3-L1细胞所经历的克隆扩增期相符。在成脂早期观察到FKBP51的合成后,我们测试了其作用终末分化过程中使用三种免疫抑制药物-环孢菌素A,FK506和雷帕霉素。脂肪细胞转化率不受环孢菌素A或FK506的影响,但在低至10 nM的药物浓度下被雷帕霉素显着降低。在药物处理的培养物中,克隆的扩增受到阻碍,在分化后期通常看到的胞浆脂质小滴的积累也受到阻碍。雷帕霉素治疗同样抑制CCAAT /增强子结合蛋白α(3T3-L1细胞分化所需的转录因子)的表达。高FK506浓度可逆转所有这三种作用,表明该操作性抑制事件是由免疫亲和素-雷帕霉素复合物介导的。 [参考:46]

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