Fig. 5.
Fig. 5. Adhesion of αXβ2-expressing CHO cells to αEC and D100. / (A) Calcein-labeled cells (0.1 mL; 5 × 105cells/mL) were added to the wells of 96-well microtiter plates coated with various concentrations of αEC (●) and D100 (▿) and postcoated with 1% PVP. After the cells were allowed to adhere for 25 minutes at 37°C, nonadherent cells were removed by 3 washes with phosphate-buffered saline and the number of adherent cells was determined by measuring the fluorescence. (B) Effect of mAbs and NIF on adhesion of cells to wells coated with 10 μg/mL αEC. The cells were preincubated with 10 μg/mL mAb IB4, 10 μg/mL mAb 3.9, or 2 μg/mL NIF for 15 minutes at 22°C. Aliquots of cells were then added to wells coated with αEC. Results are the total numbers of adherent cells and the mean ± SE values from 2 individual experiments.

Adhesion of αXβ2-expressing CHO cells to αEC and D100.

(A) Calcein-labeled cells (0.1 mL; 5 × 105cells/mL) were added to the wells of 96-well microtiter plates coated with various concentrations of αEC (●) and D100 (▿) and postcoated with 1% PVP. After the cells were allowed to adhere for 25 minutes at 37°C, nonadherent cells were removed by 3 washes with phosphate-buffered saline and the number of adherent cells was determined by measuring the fluorescence. (B) Effect of mAbs and NIF on adhesion of cells to wells coated with 10 μg/mL αEC. The cells were preincubated with 10 μg/mL mAb IB4, 10 μg/mL mAb 3.9, or 2 μg/mL NIF for 15 minutes at 22°C. Aliquots of cells were then added to wells coated with αEC. Results are the total numbers of adherent cells and the mean ± SE values from 2 individual experiments.

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