Research Paper Volume 14, Issue 17 pp 6905—6916

NOX4 promotes Kupffer cell inflammatory response via ROS-NLRP3 to aggravate liver inflammatory injury in acute liver injury

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Figure 4. Suppressing NOX4 inhibits inflammatory factor expression and NLRP3 activation. (A) Results of cell viability assay (n = 3). GKT improved the cell viability, which was higher than that in L/N group. *P < 0.05, compared with Con group; #P < 0.05, compared with L/N group. (BD) Expression of inflammatory factors (n = 3). GKT reduced the expression of inflammatory factors. The levels of IL-6, TNF-α and IL-1β in L/N + GKT group markedly decreased, lower than those in L/N group. *P < 0.05, compared with Con group; #P < 0.05, compared with L/N group. (E, F) Detection of protein expression (n = 3). After GKT suppressed NOX4, the activation of NLRP3 inflammasome was suppressed, and the expression of NLRP3, ASC and Caspase-1 decreased, significantly lower than that in L/N group. *P < 0.05, compared with Con group; #P < 0.05, compared with L/N group.