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. 2021 Feb 10;7:31. doi: 10.1038/s41420-021-00404-4

Fig. 6. Activation of NLRP3 pathway reverses the protection of ERP 44 against H/R injury.

Fig. 6

A CCK-8 was used to detect cell viability; B ELISA was used to detect the levels of IL-1β and IL-18 in cells; C western blot was used to detect the levels of pyroptosis markers in cells. Nig represents an activator of NLRP3. *p < 0.05, **p < 0.01, ***p < 0.001. All experiments were performed three times independently. Data were analyzed using two-way ANOVA and Tukey’s multiple comparison test.