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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: J Cell Biochem. 2015 Jan;116(1):22–36. doi: 10.1002/jcb.24895

Fig. 3. Effect of PP2 and PP3 on the ability of TPA or a physiological concentration of CCK (0.3 nM) to stimulate various kinases (Src, PYK2, p125FAK, paxillin and PKD).

Fig. 3

Rat pancreatic acinar cells were pretreated with no additions or with PP2 (10 µM) or PP3 (10 µM) for 1 h and then incubated with 0.3 nM CCK or TPA (1 µM). The whole cell lysates were processed as described in the Figure 1 legend. Membranes were analyzed using anti-pY416 Src, pY402 PYK2, pY397 p125FAK, pY118 paxillin and pY744/748 PKD. Both a representative experiment of 3 others and the means of all the experiments are shown. * P< 0.05 vs control, # P< 0.05 vs PP2 alone, ∞ P< 0.05 vs PP3 alone and $ P< 0.05 comparing stimulants (CCK or TPA) vs stimulants pre-incubated with PP2 or PP3, respectively.