Fig. 7.
Fig. 7. Contribution of 4 and α5integrin subunits to FN adhesion. Drug-sensitive (8226/S), melphalan-resistant (8226/LR5), and doxorubicin-resistant (8226/DOX6) were adhered to FN-coated wells (horizontal striped bars) for 1 hour. In order to determine percentage binding due to 4 and 5, some cells were pre-incubated with 4function blocking Ab P4G9 (hatched bars) or 5 function blocking Ab P1D6 (vertical striped bars) for 15 minutes before application to wells. FN adhesion by 8226/S was found to be mediated equally by 4 and 5, while FN adhesion for both drug-resistant cell lines was mediated only by 4(P < .05), as determined by complete inhibition of adherence using the 4 blocking Ab. Total FN adhesion mediated by 4 was also higher in drug-resistant lines compared with drug-sensitive 8226/S (P < .05). Values shown are the percentage of total cells applied to each well corrected for nonspecific adhesion to BSA-coated wells. Bars are the SD of n = 6 from three different experiments.

Contribution of 4 and α5integrin subunits to FN adhesion. Drug-sensitive (8226/S), melphalan-resistant (8226/LR5), and doxorubicin-resistant (8226/DOX6) were adhered to FN-coated wells (horizontal striped bars) for 1 hour. In order to determine percentage binding due to 4 and 5, some cells were pre-incubated with 4function blocking Ab P4G9 (hatched bars) or 5 function blocking Ab P1D6 (vertical striped bars) for 15 minutes before application to wells. FN adhesion by 8226/S was found to be mediated equally by 4 and 5, while FN adhesion for both drug-resistant cell lines was mediated only by 4(P < .05), as determined by complete inhibition of adherence using the 4 blocking Ab. Total FN adhesion mediated by 4 was also higher in drug-resistant lines compared with drug-sensitive 8226/S (P < .05). Values shown are the percentage of total cells applied to each well corrected for nonspecific adhesion to BSA-coated wells. Bars are the SD of n = 6 from three different experiments.

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