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. Author manuscript; available in PMC: 2019 May 15.
Published in final edited form as: J Immunol. 2018 Apr 13;200(10):3626–3634. doi: 10.4049/jimmunol.1701386

Figure 2. IFN-γ promotes a novel form of cell death in Salmonella-infected non-phagocytic cells.

Figure 2

(A) Wild-type or caspase1−/−caspase11−/− double knockout MEFs were infected with Salmonella (MOI 10) and exposed to IFN-γ (10ng/ml) with or without the presence of caspase-1 inhibitor YVAD (10uM), and cell viability was determined 48 h.p.i. (B) Wild-type and caspase1/11 double knockout bone-marrow derived macrophages (BMDMs) were infected with Salmonella (MOI 25) and cell viability was determined after 90 minutes. (C) Wild-type MEFs were infected with Salmonella (MOI 10) and exposed to IFN-γ (10ng/ml) in the presence of RIPK1 inhibitor GSK’963 (5uM), RIPK3 inhibitor GSK’843 (5uM), pan-caspase inhibitor zVAD (50uM), PI3K inhibitor 3-MA (5mM), erstatin inhibitor Ferrostatin (2.5uM) and cell viability was determined 48 h.p.i. (D) ripk3−/−, ripk3−/−casp8−/− double knockout, fadd−/−mlkl−/− double knockout, sting goldenticket mutant, tnfr1−/−zbp1−/− double knockout trif−/−, mavs−/− or atg5−/− knockout MEFs, along with wild-type controls, were infected with Salmonella in the presence of IFN-γ (10ng/ml) and cell viability was determined 48 h.p.i. Viability data shown in this figure are representative of at least three independent experiments. Error bars represent mean +− SD. **p<0.005