Table 2.

Checkerboard Analysis of Lp(a)-Induced Monocyte Migration Across Polycarbonate Membranes

Below MembraneAbove Membrane
HBSSLp(a) 33Lp(a) 100 (μg/mL)Lp(a) 300
HBSS 5.0 ± 0.6 8.3 ± 0.6 7.6 ± 0.2 7.6 ± 0.9 
Lp(a) (μg/mL) 
33 10.4 ± 1.1 8.3 ± 0.6 8.3 ± 0.5 7.7 ± 0.3 
100 15.0 ± 0.8* 12.8 ± 0.8 9.6 ± 0.5 7.2 ± 0.5 
300 23.9 ± 1.1* 20.8 ± 0.9* 16.0 ± 1.1* 9.6 ± 2.2 
Below MembraneAbove Membrane
HBSSLp(a) 33Lp(a) 100 (μg/mL)Lp(a) 300
HBSS 5.0 ± 0.6 8.3 ± 0.6 7.6 ± 0.2 7.6 ± 0.9 
Lp(a) (μg/mL) 
33 10.4 ± 1.1 8.3 ± 0.6 8.3 ± 0.5 7.7 ± 0.3 
100 15.0 ± 0.8* 12.8 ± 0.8 9.6 ± 0.5 7.2 ± 0.5 
300 23.9 ± 1.1* 20.8 ± 0.9* 16.0 ± 1.1* 9.6 ± 2.2 

Monocytes were permitted to migrate for 90 minutes across polycarbonate membranes with a pore size of 5 μm. Different concentrations of Lp(a) were placed in the upper and/or lower compartment of the Transwell chambers. Cell numbers represent the mean ± SEM of migrated monocytes in seven oil immersion fields counted in triplicates from four experiments.

*

P < .01 and † P < .05 by Newman-Keuls test versus corresponding values with HBSS in the lower compartment of the chemotaxis chamber.

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