Figure 6.
Figure 6. Constitutively active Fyn bypasses the block of TCR-dependent JNK activation by NSAIDs. (A) Immunoblot analysis of postnuclear supernatants from Jurkat cells stably transfected with empty vector or a construct encoding either F528Fyn or F505Lck. The filters were sequentially probed with anti-Fyn or anti-Lck and antitubulin mAb. Below is an antiphosphotyrosine immunoblot of the 3 lines, subsequently reprobed with antitubulin mAb. (B-C) Immunoblot analysis of postnuclear supernatants from Jurkat cells stably transfected with empty vector or a construct encoding either F528Fyn (B) or F505Lck (C), either nonactivated (0) or activated by CD3 (CD3) ligation for 5 minutes, in the presence or absence of 15 μM sc-560. Each filter was sequentially probed by immunoblot with antiphospho–JNK and then, after stripping, with control antitubulin mAb. The migration of molecular mass markers is shown.

Constitutively active Fyn bypasses the block of TCR-dependent JNK activation by NSAIDs. (A) Immunoblot analysis of postnuclear supernatants from Jurkat cells stably transfected with empty vector or a construct encoding either F528Fyn or F505Lck. The filters were sequentially probed with anti-Fyn or anti-Lck and antitubulin mAb. Below is an antiphosphotyrosine immunoblot of the 3 lines, subsequently reprobed with antitubulin mAb. (B-C) Immunoblot analysis of postnuclear supernatants from Jurkat cells stably transfected with empty vector or a construct encoding either F528Fyn (B) or F505Lck (C), either nonactivated (0) or activated by CD3 (CD3) ligation for 5 minutes, in the presence or absence of 15 μM sc-560. Each filter was sequentially probed by immunoblot with antiphospho–JNK and then, after stripping, with control antitubulin mAb. The migration of molecular mass markers is shown.

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