Figure 5
Figure 5. Analysis of MPs from HPAF-II and HPAC cells. (A) Nude mice were injected intravenously with 100 μL of HPAF-II MPs (1 ng of TF activity) or HPAC MPs (1 ng of TF activity), blood was collected immediately (n = 2) or after 2 minutes (n = 3), and human TF activity in isolated MPs was determined. (B) Nude mice were injected intravenously with 100 μL of PBS (n = 6), HPAF-II MPs (1 ng of TF activity, n = 6), or HPAC MPs (1 ng of TF activity, n = 6), and blood was collected 15 minutes later. Plasma TAT levels were measured and results are shown as dot plots with means ± SEM. *P < .05. (C) MUC-1 expression on MPs from HPAF-II and HPAC cells. MPs in serum-free culture medium from HPAF-II and HPAC cells were incubated with FITC labeled anti–human MUC-1 Ab or FITC-labeled isotype control. Stained MPs were analyzed with an LSRII flow cytometer. Results are shown as histograms of the log fluorescence intensity.

Analysis of MPs from HPAF-II and HPAC cells. (A) Nude mice were injected intravenously with 100 μL of HPAF-II MPs (1 ng of TF activity) or HPAC MPs (1 ng of TF activity), blood was collected immediately (n = 2) or after 2 minutes (n = 3), and human TF activity in isolated MPs was determined. (B) Nude mice were injected intravenously with 100 μL of PBS (n = 6), HPAF-II MPs (1 ng of TF activity, n = 6), or HPAC MPs (1 ng of TF activity, n = 6), and blood was collected 15 minutes later. Plasma TAT levels were measured and results are shown as dot plots with means ± SEM. *P < .05. (C) MUC-1 expression on MPs from HPAF-II and HPAC cells. MPs in serum-free culture medium from HPAF-II and HPAC cells were incubated with FITC labeled anti–human MUC-1 Ab or FITC-labeled isotype control. Stained MPs were analyzed with an LSRII flow cytometer. Results are shown as histograms of the log fluorescence intensity.

Close Modal

or Create an Account

Close Modal
Close Modal