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. 2005 Mar 21;102(13):4896–4901. doi: 10.1073/pnas.0500998102

Table 1. Effects of PJ in cultured human coronary artery EC exposed to shear stress generated in vitro (0, 1, 5, and 15 dynes per cm2) on e-NOS, ELK-1, and the p-JUN protein levels measured by Western blot.

Control, dyne
7 μl of PJ, dyne
14 μl of PJ, dyne
0 1 5 15 0 1 5 15 0 1 5 15
eNOS 2.1 ± 0.4 3.0 ± 0.5* 2.5 ± 0.5 2.3 ± 0.3 2.2 ± 0.5 3.3 ± 0.5 3.1 ± 0.5 2.8 ± 0.4 2.3 ± 0.5 4.1 ± 0.6 3.0 ± 0.6 3.0 ± 0.5
ELK-1 2.0 ± 0.4 3.2 ± 0.5 4.0 ± 0.6§ 5.3 ± 0.5§ 2.0 ± 0.3 2.6 ± 0.4 3.0 ± 0.6 3.7 ± 0.3 1.9 ± 0.4 2.4 ± 0.3 2.8 ± 0.4 3.3 ± 0.4
p-JUN 1.0 ± 0.3 1.3 ± 0.3 1.8 ± 0.3* 2.0 ± 0.4* 0.9 ± 0.2 1.1 ± 0.2 1.6 ± 0.4 2.0 ± 0.3 0.8 ± 0.3 1.0 ± 0.4 1.5 ± 0.4 1.6 ± 0.3

Control untreated EC or EC treated with PJ diluted in the cellular medium were exposed to laminar shear stress for 24 hours. Densitometric analysis of blots normalized with γ-tubulin are representative of the mean ± SD of five different experiments. p, significance by Bonferroni's corrected t test.

*

P <0.05 vs. 0 dyne.

P <0.05 vs. respective force in control untreated cells.

P <0.01 vs. respective force in control untreated cells.

§

P <0.001 vs. 0 dyne.

P <0.02 respective force in control untreated cells.

P <0.01 vs. respective force in control untreated cells.