Figure 5.
Figure 5. Effect of exposing HUVECs to flow on their expression of genes for chemokines and adhesion receptors in response to TNF. (A) Stained gels showing DNA amplified by RT-PCR from mRNA extracted from HUVECs that were cultured for 26 hours under static conditions (S) or exposed to shear stress of 0.3 Pa or 2 Pa (F). TNF (100 U/mL) was added for the last 2 hours. Actin is shown as a loading control unmodified by treatment. Gels are from individual experiments, which were carried out on 3 occasions. (B) Densitometry of DNA bands obtained by RT-PCR for HUVECs treated with 100 U/mL TNF and cultured under static conditions or exposed to shear stress of 0.3 Pa or 2.0 Pa. Data are mean ± SEM from 3 experiments under each condition. ANOVA showed significant effect of culture conditions on expression of IL-8, GRO-α, and E-selectin (*P < .05, **P < .01).

Effect of exposing HUVECs to flow on their expression of genes for chemokines and adhesion receptors in response to TNF. (A) Stained gels showing DNA amplified by RT-PCR from mRNA extracted from HUVECs that were cultured for 26 hours under static conditions (S) or exposed to shear stress of 0.3 Pa or 2 Pa (F). TNF (100 U/mL) was added for the last 2 hours. Actin is shown as a loading control unmodified by treatment. Gels are from individual experiments, which were carried out on 3 occasions. (B) Densitometry of DNA bands obtained by RT-PCR for HUVECs treated with 100 U/mL TNF and cultured under static conditions or exposed to shear stress of 0.3 Pa or 2.0 Pa. Data are mean ± SEM from 3 experiments under each condition. ANOVA showed significant effect of culture conditions on expression of IL-8, GRO-α, and E-selectin (*P < .05, **P < .01).

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