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. 1998 Jul;18(7):4209–4220. doi: 10.1128/mcb.18.7.4209

FIG. 11.

FIG. 11

(A) Syk−/− macrophages display reduced phosphorylation of p42 Erk-2 after FcγR engagement. Activation of Erk-2 MAPK was visualized by the phosphorylation-induced mobility shift. Macrophages were allowed to bind to IgG-RBC, and after the indicated incubation times, cells were lysed and tested for the presence of doubly threonine-tyrosine-phosphorylated forms of Erk-2 by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. (B) Induction of NOS2 (iNOS) by LPS-gamma interferon is normal in Syk-deficient macrophages. Macrophage cultures were induced with 10-μg/ml LPS and 2-U/ml gamma interferon for 16 h. At the end of the incubation period, cells were lysed and probed for the presence of NOS2 by Western blotting. WT, wild type.