Fig. 4. TFPI blocks movement of LPS to sCD14 in the absence of LBP. (A) Time course. BODIPY-LPS (0.2 μg/mL) was incubated with sCD14 (5 μg/mL) alone (•), sCD14 plus rTFPI (20 μg/mL; ▪), or PBS alone (▴) at 37°C, and fluorescence was measured at different time points before and after adding SDS. RF(%) was calculated as described above. (B) Dose dependence. BODIPY-LPS transfer to sCD14 in the absence of LBP was performed in the presence of different doses of rTFPI. The concentration of BODIPY-LPS was 0.2 μg/mL and the concentration of sCD14 was 2.5 μg/mL. The samples were incubated at 37°C for 2 hours. (▵) A control sample with BODIPY-LPS alone without sCD14. (C) sCD14-LPS complexes formed in the presence of TFPI fail to activate PMN. The PMN adhesion assay was performed with sCD14-LPS complex prepared as follows. sCD14 and LPS (100 μg/mL and 5 μg/mL in PBS, respectively) were incubated at 37°C for 2 hours. Different amounts of rTFPI were added to the samples during (▪) or after (•) the 2 hours of incubation and the resulting mixture was added to the PMN adhesion assay. For stimulation of PMN, samples were diluted to yield a final concentration of 2 μg/mL sCD14, 0.1 μg/mL LPS, and the indicated amount of rTFPI. (▴) Control samples in which LPS alone was incubated with rTFPI without sCD14. (○) Buffer alone was added to PMN for the control of PMN adhesion assay.
Fig. 4.

TFPI blocks movement of LPS to sCD14 in the absence of LBP. (A) Time course. BODIPY-LPS (0.2 μg/mL) was incubated with sCD14 (5 μg/mL) alone (•), sCD14 plus rTFPI (20 μg/mL; ▪), or PBS alone (▴) at 37°C, and fluorescence was measured at different time points before and after adding SDS. RF(%) was calculated as described above. (B) Dose dependence. BODIPY-LPS transfer to sCD14 in the absence of LBP was performed in the presence of different doses of rTFPI. The concentration of BODIPY-LPS was 0.2 μg/mL and the concentration of sCD14 was 2.5 μg/mL. The samples were incubated at 37°C for 2 hours. (▵) A control sample with BODIPY-LPS alone without sCD14. (C) sCD14-LPS complexes formed in the presence of TFPI fail to activate PMN. The PMN adhesion assay was performed with sCD14-LPS complex prepared as follows. sCD14 and LPS (100 μg/mL and 5 μg/mL in PBS, respectively) were incubated at 37°C for 2 hours. Different amounts of rTFPI were added to the samples during (▪) or after (•) the 2 hours of incubation and the resulting mixture was added to the PMN adhesion assay. For stimulation of PMN, samples were diluted to yield a final concentration of 2 μg/mL sCD14, 0.1 μg/mL LPS, and the indicated amount of rTFPI. (▴) Control samples in which LPS alone was incubated with rTFPI without sCD14. (○) Buffer alone was added to PMN for the control of PMN adhesion assay.

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