HA-tagged Cas FL and Cas ΔSH3 (Fig. 4A)28 were retrovirally introduced into NP31 cells, and the expression levels of their protein products were examined by western blotting with an anti-HA antibody that detects exogenous Cas and Selleckchem Sorafenib also with an anti-Cas antibody that detects endogenous and exogenous Cas. As shown in Fig. 4B, Cas FL and Cas ΔSH3 were expressed at almost comparable levels (left panel) that were approximately 5 to 6 times greater than those of endogenous Cas (right panel). To examine the effect of SH3 deletion on Cas-mediated signaling, cells were plated onto fibronectin (FN)-coated dishes, and the cell lysates were subjected to immunoprecipitation

followed by western blotting. As shown in Fig. 4C, anti-HA and anti-Cas2 immunoprecipitates blotted by an anti-phosphotyrosine antibody (4G10) Selleck Target Selective Inhibitor Library showed that Cas ΔSH3 was much less tyrosine-phosphorylated than Cas FL (left panel), and tyrosine phosphorylation of endogenous Cas was barely detectable in Cas ΔSH3–expressing cells (right

panel). In addition, as shown in Fig. 4D, anti-CrkII immunoprecipitates blotted by anti-HA or anti-Cas2 antibodies revealed that Cas ΔSH3 was far less efficiently coprecipitated with CrkII than Cas FL (left panel), and CrkII did not detectably coprecipitate endogenous Cas in lysates from Cas ΔSH3–expressing cells (right panel). These findings indicate that Cas ΔSH3 functions as a reduction-of-function molecule in NP31 cells as CasΔex2/Δex2 does in mouse embryonic fibroblasts (MEFs).32 To examine the suppressive function of Cas ΔSH3 on actin stress fiber formation, parental,

Cas FL–expressing, and Cas ΔSH3–expressing NP31 cells were subjected to cytoskeletal staining. As shown in Fig. 5A, prominent actin stress fiber formation was detected in parental cells and to a comparable extent in Cas FL–expressing cells (indicated by arrows in the lower left and middle panels). In contrast, no obvious actin stress fibers were formed and only dotlike actin filaments were observed in Cas ΔSH3–expressing NP31 cells (indicated by arrowheads in the lower right panel). We then investigated the formation Liothyronine Sodium of fenestrae in NP31 cells by electron microscopy because the architectural control of fenestrae is regulated by the actin cytoskeleton.1, 3, 7 Parental and Cas FL–expressing NP31 cells exhibited a number of fenestrae of various diameters (left and middle panels in Fig. 5B). Counting of the fenestrae per square micrometer showed that although the number of fenestrae in Cas FL–expressing cells was slightly higher than that in parental cells (5.80 ± 0.37 for parental cells and 6.13 ± 0.39 for Cas FL–expressing NP31 cells), the difference was not statistically significant (left and middle bars in Fig. 5C).