Where indicated, the cells were preincubated with LY294002 (20 μM) for 60 min prior to infection with H. Lazertinib solubility dmso pylori (ATCC 49503). They were infected subsequently with H. pylori for 24 h. Luciferase activity was assayed for each sample. Readings were normalized for each sample as expressed κB-LUC over constitutively expressed phRL-TK and plotted as -fold stimulation. (B) Dominant-negative Akt blocked H.
pylori signaling to an NF-κB-dependent promoter. MKN45 cells were cotransfected with κB-LUC and phRL-TK, together with either a vector or a construct expressing selleck screening library a dominant-negative Akt (Akt K179A/T308A/S473A). The cells were infected with H. pylori (ATCC 49503) 24 h later. Data are mean ± SD of three independent experiments. PI3K inhibition or transfection with small interference RNAs for p65 and Akt suppresses H. pylori-induced IL-8 expression Finally, we investigated the effect of inhibition of H. pylori-induced PI3K activity on IL-8
expression. Pretreatment of MKN45 cells with LY294002 reduced H. pylori-stimulated IL-8 mRNA expression as determined Selinexor concentration by reverse transcription-polymerase chain reaction (RT-PCR) (Figure 6A). Inhibition of PI3K also significantly decreased the amount of IL-8 secreted by MKN45 cells stimulated with H. pylori in a dose-dependent manner (Figure 6B). Figure 6 LY294002 inhibits H. pylori -induced IL-8 expression and production. (A) MKN45 cells were preincubated with LY294002 (20 μM) for 60 min prior to infection with H. pylori (ATCC 49503), harvested at the indicated time points and assayed for IL-8 mRNA expression by RT-PCR. Lane M contains markers. (B) LY294002 inhibits H. pylori-induced
IL-8 production. MKN45 cells were preincubated with the indicated concentrations of LY294002 for 60 min prior to infection with H. pylori (ATCC 49503). For IL-8 protein determination, supernatants were collected 24 h after infection and assessed for IL-8 production by ELISA. Data are mean ± SD of three experiments. LY294002 is a chemical inhibitor, and thus its target specifiCity may be Histone demethylase questionable. Thus, small interference RNAs (siRNAs) for p65 and Akt were used to examine the role of p65 and Akt activation in the signal transduction pathway leading to IL-8 expression by H. pylori infection. Each siRNA specifically inhibited the expression of p65 and Akt (Figure 7). Figure 7 also shows that H. pylori-induced IL-8 mRNA expression was inhibited by siRNAs for p65 and Akt, confirming that p65 and Akt are important in H. pylori-induced IL-8 expression. Figure 7 Transfection of siRNAs for p65 and Akt inhibits H. pylori -induced IL-8 expression. MKN45 cells were transfected with siRNAs for p65 and Akt, followed by stimulation with H. pylori (ATCC 49503) for 6 h. The RNA was subjected to RT-PCR for IL-8 and p65 mRNAs. Lane M contains markers.