Key result
In vitro treatment of cultured HUVECs with cigarette smoking extracts resulted in a significant reduction in NO levels (P<0.001), while genotype-dependent eNOS mRNA expression was maintained (P<0.05).
p-value: p=<0.001
Endothelial cells maintain genotype-dependent eNOS expression in vitro, but the interaction between genotype and cigarette smoking may require in vivo conditions to manifest.
DNA polymorphisms in endothelial nitric oxide synthase (eNOS) gene have been shown to be associated with constitutive eNOS expression and coronary artery disease (CAD). In the present study we explored the hypothesis whether genotype-dependent effects can be maintained in vitro during replication, or the effect is conditional on in vivo biological environments. Human umbilical vein endothelial cells (HUVEC) were collected and cultured from 89 normal deliveries of Mexican Americans. The cells were treated with or without cigarette smoking extracts (CSE) and genotypes of eNOS polymorphisms were determined by PCR. We measured the levels of eNOS by ELISA and its binding proteins including heat-shock protein 90 (Hsp-90) and caveolin-1 by Western blotting. The rare C allele for the promoter T786C polymorphism (0.2), and the rare 4 x 27-bp repeat allele in the intron 4 (0.30) were different from those reported in other populations. Yet, the rare T allele in the exon 7 (G894T polymorphism) was similar as others. After four passages in vitro, both the intron 4 and promoter polymorphisms maintained significant effects on eNOS mRNA levels in HUVECs (P < 0.05). However, the effects on eNOS protein and enzyme activity were less consistent. Although primary smokers had significantly lower eNOS protein levels (P < 0.05), the in vitro CSE treatment on cultured HUVECs only resulted in a significant reduction in NO levels as measured by the stable metabolites of nitrite/nitrate (P < 0.001). Neither Hsp-90 nor caveolin-1--important eNOS regulators--appears to mediate the genotypesmoking effects on eNOS expression although HUVECs did produce more Hsp-90 when exposed to CSE. Our study demonstrates that endothelial cells maintain genotype-dependent expression even after the deprivation of in vivo environment. However, the cigarette smoking-genotype interaction may require such in vivo conditions to be manifested.
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Duraisamy et al. (2005) studied Normal deliveries (n=89). Cigarette smoking extracts (CSE) vs. Without cigarette smoking extracts was evaluated on NO levels measured by stable metabolites of nitrite/nitrate (p=<0.001). In vitro treatment of cultured HUVECs with cigarette smoking extracts resulted in a significant reduction in NO levels (P<0.001), while genotype-dependent eNOS mRNA expression was maintained (P<0.05).
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