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. 2022 Dec 14;11(12):2461. doi: 10.3390/antiox11122461

Figure 4.

Figure 4

Knockdown of IKKα decreases NF-κB/IL-1β signaling in THP-1 cells. (A) Viability of H2O2 (0–30 μM)-treated THP-1 cells based on the WST-1 assay. (B) Levels of ROS measured by DCFH-DA staining. (C) mRNA levels of IL-1β in H2O2 (0–20 μM)-treated THP-1 cells. (D) mRNA level of IL-1β. THP-1 cells were transfected with siRNA-targeting IKKα (siIKKα) or scrambled sequence (siCtrl) for 12 h. BMS-345541 was used to block IKKα/β. The cells were then stimulated (or not) with H2O2 (5 μM) for 24 h. The cells were harvested for qRT-PCR assay or (E) immunoblotting. (F) Quantification of immunoblotting. Data are expressed as the mean ± SEM (n = 4). * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control or 0 μM group. # p < 0.05, ## p < 0.01, ### p < 0.001 vs. H2O2 group.