Figure 5. Inhibition of JNK Prevents Inflammasome Activation in PTPN2-LysMCre Mice.
(A) BMDMs from WT, PTPN2-LysMCre, and ASC–/– mice were left untreated or activated with MSU for 2 hr and lysates analyzed for JNK and Syk phosphorylation and expression of PTPN2, ASC, and NLRP3. Each lane represents an individual mouse.
(B and C) BMDMs from WT and PTPN2-LysMCre (KO) mice were treated with Syk, JNK, or p38 inhibitors 1 hr prior to activation with MSU. Analysis of the cell culture supernatant for IL-1β secretion (B) and maturation (C) by ELISA and western blot, respectively.
(D) Precipitation of ASC from the cell lysate and analysis for tyrosine phosphorylation and co-precipitated NLRP3 and PTPN2.
Asterisks denote significant differences (*p < 0.05 and **p < 0.01; Student’s t test with Bonferroni correction). Error bars represent means ± SD. See also Figure S7.