Fig. 1.
Fig. 1. Defensin promotes the binding of Lp(a) to HUVEC matrix. (A) 125I-Lp(a) (20 nmol/L) or mixtures of defensin (10 μmol/L) plus 125I-Lp(a) (20 nmol/L) were incubated with HUVEC matrix in the presence of buffer (□, ▩) or 20-fold molar excess cold Lp(a) () for 1 hour at 37°C, and the bound radioactivity was measured. The mean ± SD of 3 experiments is shown. This corresponds to an increase in bound Lp(a) from a mean of 2.9 fmol in the absence of defensin to 96 fmol in the presence of defensin. The mean ± SD of 3 experiments is shown. (B)125I-Lp(a) (10 nmol/L) was incubated with HUVEC matrix in the presence of the indicated concentrations of defensin for 1 hour at 37°C, and the bound radioactivity was measured. The data are expressed relative to the binding of 125I-Lp(a) alone. The mean ± SD of 3 experiments is shown.

Defensin promotes the binding of Lp(a) to HUVEC matrix. (A) 125I-Lp(a) (20 nmol/L) or mixtures of defensin (10 μmol/L) plus 125I-Lp(a) (20 nmol/L) were incubated with HUVEC matrix in the presence of buffer (□, ▩) or 20-fold molar excess cold Lp(a) () for 1 hour at 37°C, and the bound radioactivity was measured. The mean ± SD of 3 experiments is shown. This corresponds to an increase in bound Lp(a) from a mean of 2.9 fmol in the absence of defensin to 96 fmol in the presence of defensin. The mean ± SD of 3 experiments is shown. (B)125I-Lp(a) (10 nmol/L) was incubated with HUVEC matrix in the presence of the indicated concentrations of defensin for 1 hour at 37°C, and the bound radioactivity was measured. The data are expressed relative to the binding of 125I-Lp(a) alone. The mean ± SD of 3 experiments is shown.

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