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Quantitative evaluation of transcriptional activation of NF-κB p65 and p50 subunits and IκBα encoding genes in colon cancer cells by Desulfovibrio desulfuricans endotoxin

机译:脱硫脱硫弧菌内毒素对结肠癌细胞中NF-κBp65和p50亚基和IκBα编码基因转录激活的定量评估

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摘要

Quantification of p65, p50 and IκBα mRNAs was performed by real time QRT-PCR in Caco-2 cells treated with 10, 50, and 100 μg/mL of Desulfovibrio desulfuricans LPS for 1, 6, 12, and 24 h. A strong increase in expression of p65 and IλBα genes was induced by 10 and 100 μg/mL of LPS at 1 h; after 6 h higher transcript amounts of both genes were observed at 100 μg/mL LPS. The p65 expression level was significantly increased by 50 and 100 μg/mL at 12 h and lowered by all LPS doses at 24 h. No significant differences between IκBα mRNA quantity in cells exposed to LPS at 12 and 24 h were observed. No changes in expression of p50 mRNA were induced by LPS. The expression of p65 gene positively correlated with IκBα gene expression. D. desulfuricans LPS is capable of modulating transcriptional activity of p65 and IκBα genes in intestinal epithelial cells.
机译:通过实时QRT-PCR在分别用10、50和100μg/ mL脱硫弧菌LPS处理1,6、12和24 h的Caco-2细胞中对p65,p50和IκBαmRNA进行定量。在1 h时,10和100μg/ mL的LPS诱导p65和IλBα基因的表达大量增加; 6小时后,在100μg/ mL LPS下观察到两个基因的更高转录物量。 p65的表达水平在12 h时显着增加50和100μg/ mL,在24 h时所有LPS剂量均降低。在12和24 h暴露于LPS的细胞中,IκBαmRNA量之间没有显着差异。 LPS不会诱导p50 mRNA表达的变化。 p65基因的表达与IκBα基因的表达呈正相关。 D. desulfuricans LPS能够调节肠上皮细胞中p65和IκBα基因的转录活性。

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