TABLE 2

Effects of the src-inhibitor PP1 on VCAM-1 and ICAM-1 expression upon gly-LDL and dm-LDL stimulation

VCAM-1 expressionICAM-1 expression
Control 35.79 ± 5.72 25.15 ± 1.30 
gly-LDL 61.07 ± 1.51* 26.33 ± 1.00 (NS) 
gly-LDL + PP1 55.10 ± 0.30 (NS) 25.80 ± 3.68 (NS) 
dm-LDL 59.21 ± 2.50* 27.65 ± 3.22 (NS) 
dm-LDL + PP1 56.11 ± 1.25 (NS) 26.80 ± 2.30 (NS) 
TNF-α 59.20 ± 2.55* 78.40 ± 5.33* 
VCAM-1 expressionICAM-1 expression
Control 35.79 ± 5.72 25.15 ± 1.30 
gly-LDL 61.07 ± 1.51* 26.33 ± 1.00 (NS) 
gly-LDL + PP1 55.10 ± 0.30 (NS) 25.80 ± 3.68 (NS) 
dm-LDL 59.21 ± 2.50* 27.65 ± 3.22 (NS) 
dm-LDL + PP1 56.11 ± 1.25 (NS) 26.80 ± 2.30 (NS) 
TNF-α 59.20 ± 2.55* 78.40 ± 5.33* 

Data are means ± SEM of % fluorescent cells of 6 individual experiments. ECs were incubated with vehicle alone, with gly-LDL or with dm-LDL (100μg/ml), with or without PP1 (5umol/l). Tumor necrosis factor-α (TNF-α) (10nmol/l) was used as positive control. The cells were stained with an anti-VCAM antibody or with an anti-ICAM antibody. The expression of the corresponding protein was evaluated by fluorescence-activated cell sorter. ANOVA with Newman-Keuls multicomparison test was performed for control vs. experimental groups.

*

P < 0.05; NS not significant, P > 0.05.

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