Figure 5.
Figure 5. Evaluation for p110δ protein and activity in thymocytes. (A) Representative immunoblots of class 1a and 1b p110 subunits expressed in thymocytes harvested from WT control and p110γδ-/- mice. Western blot of β-actin illustrates equal loading of proteins. (B) Detection of Akt/PKB in Western blots of total lysates from p110γ-/- thymocytes treated with vehicle control or the p110δ-specific inhibitor IC87114 (10 μM) before TCR cross-linking. (C) Ca2+ flux in CD4+-gated thymocytes in WT control, p110γ-/-, p110δ-/-, and p110γδ-/- mice in response to TCR cross-linking. Ca2+ flux in CD4+CD8+-sorted thymocytes from WT control and p110γδ-/- animals is shown for comparison (inset). Data are representative of 3 to 4 separate experiments.

Evaluation for p110δ protein and activity in thymocytes. (A) Representative immunoblots of class 1a and 1b p110 subunits expressed in thymocytes harvested from WT control and p110γδ-/- mice. Western blot of β-actin illustrates equal loading of proteins. (B) Detection of Akt/PKB in Western blots of total lysates from p110γ-/- thymocytes treated with vehicle control or the p110δ-specific inhibitor IC87114 (10 μM) before TCR cross-linking. (C) Ca2+ flux in CD4+-gated thymocytes in WT control, p110γ-/-, p110δ-/-, and p110γδ-/- mice in response to TCR cross-linking. Ca2+ flux in CD4+CD8+-sorted thymocytes from WT control and p110γδ-/- animals is shown for comparison (inset). Data are representative of 3 to 4 separate experiments.

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