首页> 美国卫生研究院文献>Cancer Cell International >Sirtuin 1 inhibits lipopolysaccharide-induced inflammation in chronic myelogenous leukemia k562 cells through interacting with the Toll-like receptor 4-nuclear factor κ B-reactive oxygen species signaling axis
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Sirtuin 1 inhibits lipopolysaccharide-induced inflammation in chronic myelogenous leukemia k562 cells through interacting with the Toll-like receptor 4-nuclear factor κ B-reactive oxygen species signaling axis

机译:Sirtuin 1通过与Toll样受体4核因子κB反应性氧信号转导轴相互作用抑制脂多糖诱导的慢性粒细胞白血病k562细胞的炎症

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摘要

LPS-triggered production of proinflammatory cytokines in k562 cells. Cytokines and chemokines in LPS-treated k562 cells were detected using qPCR, ELISA, and WB. Influence of LPS treatment on mRNA expressions of inflammatory cytokines in k562 cells determined via qPCR. qPCR was performed to examine the mRNA expression of inflammatory cytokines after LPS treatment in k562 cells. In qPCR, gene expressionin each group was first normalized to the GAPDH gene, and then normalized to the data of the control group. Influence of LPS treatment on the protein expressions of inflammatory cytokines in k562 cells determined via ELISA. , Influence of LPS treatment on protein levels of IL-1β, IL-6, and TNF-α in both k562 and KU812 cells determined via WB analyses. Data are expressed as mean ± standard deviation. *P
机译:LPS触发了k562细胞中促炎细胞因子的产生。使用qPCR,ELISA和WB检测LPS处理的k562细胞中的细胞因子和趋化因子。 LPS处理对通过qPCR测定的k562细胞中炎性细胞因子mRNA表达的影响。进行qPCR以检查LPS处理后在k562细胞中炎性细胞因子的mRNA表达。在qPCR中,首先将各组的基因表达标准化为GAPDH基因,然后再将其标准化为对照组的数据。 LPS处理对通过ELISA测定的k562细胞中炎性细胞因子蛋白表达的影响。 ,通过WB分析确定LPS处理对k562和KU812细胞中IL-1β,IL-6和TNF-α蛋白质水平的影响。数据表示为平均值±标准偏差。 * P

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