Fig. 9.
Fig. 9. Adhesion ability of transfectants to immobilized fibrinogen. / (A) Binding of transfected CHO cells to immobilized fibrinogen. Transfected cells expressing Pro33 (solid line) and Pro33ΔLys611 (broken line) of GPIIIa were labeled with calcein-am. Labeled cells were allowed to adhere to microtiter wells coated with fibrinogen, BSA, or mAb Gi5 specific for GPIIb-IIIa complex. After washing, adherent cells were measured in fluorescence microtiter plate reader. Nonspecific cell adhesion on BSA was subtracted. Cell adhesion was normalized to cell binding on Gi5 (Fg/Gi5 ratio). (B) Tyrosine phosphorylation of pp125FAK following cell adhesion to immobilized fibrinogen. Stable transfectants expressing GPIIb-IIIa Pro33 (lanes 1) and GPIIb-IIIa Pro33Δ Lys611 (lanes 2) were allowed to bind fibrinogen-coated wells. Adherent cells were lysed and precipitated with rabbit polyclonal anti-pp125FAK. Immunoprecipitates were separated on 7.5% SDS-PAGE, blotted, and probed subsequently with mAbs against phosphotyrosine (pTyr) and pp125FAK and visualized using peroxidase-labeled secondary antibody and chemiluminescence substrate.

Adhesion ability of transfectants to immobilized fibrinogen.

(A) Binding of transfected CHO cells to immobilized fibrinogen. Transfected cells expressing Pro33 (solid line) and Pro33ΔLys611 (broken line) of GPIIIa were labeled with calcein-am. Labeled cells were allowed to adhere to microtiter wells coated with fibrinogen, BSA, or mAb Gi5 specific for GPIIb-IIIa complex. After washing, adherent cells were measured in fluorescence microtiter plate reader. Nonspecific cell adhesion on BSA was subtracted. Cell adhesion was normalized to cell binding on Gi5 (Fg/Gi5 ratio). (B) Tyrosine phosphorylation of pp125FAK following cell adhesion to immobilized fibrinogen. Stable transfectants expressing GPIIb-IIIa Pro33 (lanes 1) and GPIIb-IIIa Pro33Δ Lys611 (lanes 2) were allowed to bind fibrinogen-coated wells. Adherent cells were lysed and precipitated with rabbit polyclonal anti-pp125FAK. Immunoprecipitates were separated on 7.5% SDS-PAGE, blotted, and probed subsequently with mAbs against phosphotyrosine (pTyr) and pp125FAK and visualized using peroxidase-labeled secondary antibody and chemiluminescence substrate.

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