Table 2

Inhibition of Plg binding to murine and human macrophage-related cells by Plg-R Fab

Plg-RInhibition of Plg binding, %
RAW 264.7J774A.1Mouse mФsTHP-1PMA+THP-1
H2B 50.7 ± 4 42 ± 3 48 ± 5 ND 58 ± 9 
α-Enolase 23 ± 3.5 ND 18 ± 2 12 ± 3 17 ± 7 
Annexin 2 23 ± 3 ND 20 ± 3 ND 25 ± 3 
p11 16 ± 2 ND 24 ± 4 ND 29 ± 5 
Plg-RInhibition of Plg binding, %
RAW 264.7J774A.1Mouse mФsTHP-1PMA+THP-1
H2B 50.7 ± 4 42 ± 3 48 ± 5 ND 58 ± 9 
α-Enolase 23 ± 3.5 ND 18 ± 2 12 ± 3 17 ± 7 
Annexin 2 23 ± 3 ND 20 ± 3 ND 25 ± 3 
p11 16 ± 2 ND 24 ± 4 ND 29 ± 5 

RAW 264.7 cells, J774A.1 cells, TG-induced peritoneal mouse macrophages (mФs), THP-1 (human monocytoid), or PMA-stimulated THP-1 (macrophage-like) cells were preincubated with Fab to H2B (C-terminal), α-enolase, annexin 2, or anti-p11 for 30 minutes at 4°C, followed by incubation with Alexa 488–labeled Plg (200 nM) for 60 minutes. The cells were washed and bound Plg was measured by FACS. Calculations are based on inhibition of specific Plg binding, inhibitable by EACA. The data are means plus or minus SD from 3 independent experiments.

ND indicates no detectable inhibition.

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