Fig. 4.
Fig. 4. Kinetics of EMP binding to THP-1 cells. / THP-1 cells were incubated with EMP (50:1 EMP–THP-1 ratio) and were analyzed for the presence of endothelial antigens (VCAM-1, E-selectin, endoglin) by flow cytometry. (A) Representative fluorescence histograms showing 3End mAb-positive staining of THP-1 cells incubated with EMPs for 15 minutes (EMP 3End mAbs) compared with controls. THP-1 cells incubated with control medium stained with isotype control (CM IgG1) or 3End mAbs (CM 3End mAbs), and THP-1 cells incubated with EMP stained with isotype control (EMP IgG1). (B) Representative fluorescence histogram showing staining of THP-1 cells with 3End mAbs after incubation with EMP for 5 minutes, 15 minutes, 30 minutes, and 1 hour (EMP 3End mAbs 5 minutes, 15 minutes, 30 minutes, 1hour) compared with isotype control (EMP IgG1).

Kinetics of EMP binding to THP-1 cells.

THP-1 cells were incubated with EMP (50:1 EMP–THP-1 ratio) and were analyzed for the presence of endothelial antigens (VCAM-1, E-selectin, endoglin) by flow cytometry. (A) Representative fluorescence histograms showing 3End mAb-positive staining of THP-1 cells incubated with EMPs for 15 minutes (EMP 3End mAbs) compared with controls. THP-1 cells incubated with control medium stained with isotype control (CM IgG1) or 3End mAbs (CM 3End mAbs), and THP-1 cells incubated with EMP stained with isotype control (EMP IgG1). (B) Representative fluorescence histogram showing staining of THP-1 cells with 3End mAbs after incubation with EMP for 5 minutes, 15 minutes, 30 minutes, and 1 hour (EMP 3End mAbs 5 minutes, 15 minutes, 30 minutes, 1hour) compared with isotype control (EMP IgG1).

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