Figure 4
Figure 4. Overexpression of DAPK and [K42A]DAPK increases caspase-1 activation and mature IL-1β generation. THP-1 cells were infected with pGC-YFP, pGC-YFP-DAPK, or pGC-YFP-[K42A]DAPK, and YFP-expressing cells isolated by sorting. Control (YFP) and DAPK-expressing THP-1 cells were treated with PMA for 16 hours and then stimulated with MSU (A), or R848 (B) for 6 hours. The IL-1β contents in supernatant were determined by ELISA (C). The amounts of the cleaved IL-1β, procaspase-1, caspase-1 (p10), DAPK, pro-IL-1β, and GAPDH in total cell lysates were determined by immunoblots (A-B). All experiments have been repeated 3 times with similar results. **P < .01, ***P < .001 for paired t test.

Overexpression of DAPK and [K42A]DAPK increases caspase-1 activation and mature IL-1β generation. THP-1 cells were infected with pGC-YFP, pGC-YFP-DAPK, or pGC-YFP-[K42A]DAPK, and YFP-expressing cells isolated by sorting. Control (YFP) and DAPK-expressing THP-1 cells were treated with PMA for 16 hours and then stimulated with MSU (A), or R848 (B) for 6 hours. The IL-1β contents in supernatant were determined by ELISA (C). The amounts of the cleaved IL-1β, procaspase-1, caspase-1 (p10), DAPK, pro-IL-1β, and GAPDH in total cell lysates were determined by immunoblots (A-B). All experiments have been repeated 3 times with similar results. **P < .01, ***P < .001 for paired t test.

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