Table 1.

SMCs regulate ICAM-1, VCAM-1, and E-selectin gene expression in cocultured ECs via close interaction between these cocultured cells

Adhesion
molecule
ControlShear
EC/SMCEC/slide/SMCEC/φ + medEC/φEC/SMCEC/slide/SMC
ICAM-1 561 ± 86* 98 ± 16 102 ± 16 339 ± 40* 88 ± 17 296 ± 32* 
VCAM-1 1153 ± 264* 103 ± 19 95 ± 8 92 ± 11 42 ± 11*, 95 ± 14 
E-selectin 967 ± 213* 108 ± 12 97 ± 13 124 ± 31 93 ± 16 109 ± 18 
Adhesion
molecule
ControlShear
EC/SMCEC/slide/SMCEC/φ + medEC/φEC/SMCEC/slide/SMC
ICAM-1 561 ± 86* 98 ± 16 102 ± 16 339 ± 40* 88 ± 17 296 ± 32* 
VCAM-1 1153 ± 264* 103 ± 19 95 ± 8 92 ± 11 42 ± 11*, 95 ± 14 
E-selectin 967 ± 213* 108 ± 12 97 ± 13 124 ± 31 93 ± 16 109 ± 18 

ECs cultured alone (EC/φ) or cocultured with SMCs grown on a cover slip (EC/slide/SMC) or without a cover slip (EC/SMC) were maintained in static condition or exposed to shear stress of 12 dyne/cm2 for 6 hours and their mRNA expression was determined by RT-PCR analysis, as described in “Materials and methods.” Amplification of the cDNA was performed in parallel samples using human GAPDH primers. ECs that were incubated in a static condition with culture medium collected from the EC/SMC coculture (EC/φ + med) did not significantly increase their expression of ICAM-1, VCAM-1, or E-selectin mRNA. Data on band density normalized to GAPDH RNA levels are presented as percentages of the results for the control EC/φ (taken as 100%). The results shown are mean ± SEM from 4 independent experiments in each group.

*

P < .05 vs control EC/φ.

P < .05 vs control EC/SMC.

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