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首页> 外文期刊>Cellular & molecular biology letters. >MITF and PU.1 inhibit adipogenesis of ovine primary preadipocytes by restraining C/EBPβ
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MITF and PU.1 inhibit adipogenesis of ovine primary preadipocytes by restraining C/EBPβ

机译:MITF和PU.1通过抑制C /EBPβ抑制绵羊原代前脂肪细胞的脂肪生成

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PU box-binding protein (PU.1) is a master gene of hematopoietic lineage and an important specific transcription factor in osteoclast lineage. There is proof of its expression in adipose tissue, and it is known to significantly and negatively affect adipogenesis. However, it is unclear whether there are any other molecules involved in this process. We wished to explore the effect of PU.1’s co-activator microphthalmia-associated transcription factor (MITF) on the adipogenic differentiation of ovine primary preadipocytes. The expression vectors pcDNA-MITF and pcDNA-PU.1, and MITF siRNA and PU.1 siRNA were transfected or co-transfected into ovine tail primary preadipocytes. Real-time PCR and western blot analysis were applied to investigate the expression levels of PU.1 and MITF. The morphologic changes in the cells were observed under a microscope at a magnification of × 200 after staining with Oil Red O. The triglyceride (TG) content in cells was also determined after transfection. MITF and its co-activator PU.1 synergistically exhibited an opposite expression pattern to that of CCAAT-enhancer-binding protein-β (C/EBPβ) during adipogenic differentiation of ovine primary preadipocytes. Before induction of differentiation, overexpression of MITF or PU.1 inhibited the expression of C/EBPβ and adipogenesis in the cells; and knockdown of MITF or PU.1 promoted the expression of C/EBPβ and adipogenesis in the cells. The inhibitory or promotive effect was enhanced when MITF and PU.1 were co-overexpressed or co-silenced. However, when MITF and/or PU.1 were overexpressed after day 2 of differentiation, no changes in adipogenesis of the cells were observed. MITF and its co-activator PU.1 inhibited adipogenesis of ovine primary preadipocytes by restraining C/EBPβ.
机译:PU盒结合蛋白(PU.1)是造血谱系的主要基因,是破骨细胞谱系中重要的特异性转录因子。有证据表明它在脂肪组织中表达,并且已知对脂肪形成有显着负面影响。但是,尚不清楚该过程中是否涉及其他分子。我们希望探讨PU.1的辅助激活物小眼症相关转录因子(MITF)对绵羊原代前脂肪细胞成脂分化的影响。将表达载体pcDNA-MITF和pcDNA-PU.1以及MITF siRNA和PU.1 siRNA转染或共转染到羊尾原代前脂肪细胞中。应用实时荧光定量PCR和蛋白质印迹分析来研究PU.1和MITF的表达水平。用油红O染色后,在显微镜下以×××200的放大倍数观察细胞的形态变化。转染后也测定细胞中甘油三酸酯(TG)的含量。 MITF及其辅助激活剂PU.1在绵羊原代前脂肪细胞成脂分化过程中协同表现出与CCAAT-增强子结合蛋白-β(C /EBPβ)相反的表达模式。在诱导分化之前,MITF或PU.1的过表达抑制了细胞中C /EBPβ的表达和脂肪生成。 MITF或PU.1的敲低促进了C /EBPβ的表达和细胞的脂肪形成。当MITF和PU.1共表达或共沉默时,抑制或促进作用增强。但是,当分化的第二天后MITF和/或PU.1过表达时,未观察到细胞脂肪形成的变化。 MITF及其共激活因子PU.1通过抑制C /EBPβ抑制绵羊原代前脂肪细胞的脂肪生成。

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