Figure 4.
Figure 4. Adhesion of CHO cells stably expressing normal or mutant αIIbβ3 or αvβ3 complexes to solid-phase fibrinogen or vitronectin. Approximately 4 × 105 cells were added to the wells of microtiter plates coated with ligands and incubated at 37°C.Adhesion was examined by phase-contrast microscopy as described in “Materials and methods.” (A) CHO-αIIbβ3 or CHO-αIIbβ3(616-690del) cells were seeded onto plates coated with 10 μg/mL fibrinogen and incubated for 10 minutes. (B-C) CHO-αvβ3 and CHO-αvβ3(616-690del) cells were seeded onto microtiter plates coated with 10 μg/mL vitronectin (B) or 10 μg/mL fibrinogen (C) and incubated for 30 minutes. Original magnification, × 100.

Adhesion of CHO cells stably expressing normal or mutant αIIbβ3 or αvβ3 complexes to solid-phase fibrinogen or vitronectin. Approximately 4 × 105 cells were added to the wells of microtiter plates coated with ligands and incubated at 37°C.Adhesion was examined by phase-contrast microscopy as described in “Materials and methods.” (A) CHO-αIIbβ3 or CHO-αIIbβ3(616-690del) cells were seeded onto plates coated with 10 μg/mL fibrinogen and incubated for 10 minutes. (B-C) CHO-αvβ3 and CHO-αvβ3(616-690del) cells were seeded onto microtiter plates coated with 10 μg/mL vitronectin (B) or 10 μg/mL fibrinogen (C) and incubated for 30 minutes. Original magnification, × 100.

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