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A potential role of IL-6 in the chito-oligosaccharide-mediated inhibition of adipogenesis.

机译:IL-6在壳寡糖介导的脂肪形成抑制中的潜在作用。

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Recent studies have suggested that chito-oligosaccharides can have anti-adipogenic properties. The objectives of the present study were to evaluate the anti-adipogenic potential of four different chito-oligosaccharides (molecular weight (MW) <1000, 1000-3000, 3000-5000 and 5000-10 000 Da) and to identify molecular mechanisms underlying the chito-oligosaccharide-mediated inhibition of adipogenesis. Mouse 3T3-L1 cells were allowed to differentiate in the presence of chito-oligosaccharide. At day 8 post-induction of differentiation, lipid accumulation, free glycerol release and the quantitative expression of adipogenic marker genes were evaluated. Chito-oligosaccharides had concentration- and MW-dependent inhibitory effects on lipid accumulation (P < 0.001 and < 0.05, respectively), as well as a concentration-dependent effect (P < 0.001) on free glycerol release and the expression of adipogenic marker genes. The 5000-10 000 Da chito-oligosaccharide was selected for subsequent molecular studies. A panel of forty-four lipid metabolic pathway-specific genes was analysed by quantitative real-time PCR. Chito-oligosaccharide-mediated inhibition of adipogenesis was associated with the up-regulation of the IL-6 gene at all concentrations of chito-oligosaccharide examined and the PG-endoperoxide synthase 2 (PTGS2) gene at higher concentrations of chito-oligosaccharide. The effect of chito-oligosaccharide on gene expression was validated by measuring IL-6 protein concentrations in the media. Finally, an IL-6 promoter assay was developed to characterise the effect of chito-oligosaccharide on the transcriptional activity of the IL-6 promoter, which was increased in a concentration-dependent manner (P < 0.001). We conclude that IL-6 is a candidate signalling molecule in the chito-oligosaccharide-mediated inhibition of adipogenesis in 3T3-L1 cells
机译:最近的研究表明,壳寡糖可以具有抗脂肪形成特性。本研究的目的是评估四种不同的壳寡糖(分子量(MW)<1000、1000-3000、3000-5000和5000-10 000 Da)的抗脂肪形成潜力,并确定其潜在的分子机制。壳寡糖介导的脂肪形成抑制。允许小鼠3T3-L1细胞在壳寡糖存在下分化。在诱导分化后的第8天,评估脂质蓄积,游离甘油释放和成脂标记基因的定量表达。壳寡糖对脂类积累具有浓度依赖性和MW依赖性抑制作用( P 分别为<0.001和<0.05),以及浓度依赖性作用( P <0.001)释放甘油和脂肪生成标记基因的表达。选择了5000-10 000 Da的壳寡糖用于后续的分子研究。通过定量实时PCR分析一组44种脂质代谢途径特异性基因。壳聚糖寡糖介导的脂肪形成抑制与在所有浓度的壳寡糖和PG-过氧化物合成酶2( PTGS2 )上 IL-6 基因的上调相关。 i>)基因在较高浓度的壳寡糖中。壳寡糖对基因表达的影响通过测量培养基中的IL-6蛋白浓度来验证。最后,开发了 IL-6 启动子测定法,以表征壳寡糖对 IL-6 启动子转录活性的影响,该活性随浓度的增加而增加。依赖方式( P <0.001)。我们得出结论,IL-6是壳寡糖介导的3T3-L1细胞脂肪形成抑制中的候选信号分子

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