Figure 6
Figure 6. Flow cytometry with β2GPI. Binding of open or closed β2GPI to monocytes was investigated. Cells (1 × 106 cells/mL) were incubated for 30 minutes with fluorescently labeled β2GPI ± LPS or β2GPI ± fluorescently labeled LPS. Open β2GPI (●), but not plasma-purified closed β2GPI (▴), showed a concentration- (A) and time-dependent (B) binding to monocytes (both n = 5). Incubation of plasma-purified closed β2GPI (0.2μM) with fluorescently labeled LPS showed binding of β2GPI to monocytes (; n = 3; C). Similar binding could be observed with preincubated fluorescently labeled plasma-purified β2GPI (0.2μM) and LPS (; n = 3) (D). (E) Binding of open β2GPI (0.3μM) to monocytes could be partially inhibited (approximately 70%) by addition of RAP. (F) Addition of increasing concentrations of RAP (0-10μM) also reduced the inhibitory effect of β2GPI (1μM) on LPS-induced TF expression on monocytes (n = 3). Results are expressed as mean ± SEM.

Flow cytometry with β2GPI. Binding of open or closed β2GPI to monocytes was investigated. Cells (1 × 106 cells/mL) were incubated for 30 minutes with fluorescently labeled β2GPI ± LPS or β2GPI ± fluorescently labeled LPS. Open β2GPI (●), but not plasma-purified closed β2GPI (▴), showed a concentration- (A) and time-dependent (B) binding to monocytes (both n = 5). Incubation of plasma-purified closed β2GPI (0.2μM) with fluorescently labeled LPS showed binding of β2GPI to monocytes (; n = 3; C). Similar binding could be observed with preincubated fluorescently labeled plasma-purified β2GPI (0.2μM) and LPS (; n = 3) (D). (E) Binding of open β2GPI (0.3μM) to monocytes could be partially inhibited (approximately 70%) by addition of RAP. (F) Addition of increasing concentrations of RAP (0-10μM) also reduced the inhibitory effect of β2GPI (1μM) on LPS-induced TF expression on monocytes (n = 3). Results are expressed as mean ± SEM.

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