Enhanced recovery of injury-caused downregulation of paxillin protein by eNOS gene expression in rat carotid artery - Mechanism of NO inhibition of intimal hyperplasia?
Sy. Fang et al., Enhanced recovery of injury-caused downregulation of paxillin protein by eNOS gene expression in rat carotid artery - Mechanism of NO inhibition of intimal hyperplasia?, ART THROM V, 19(1), 1999, pp. 147-152
Injury-caused dedifferentiation accompanied by proliferation and migration
of smooth muscle cells (SMCs) is an important process in the development of
the neointima. Nitric oxide (NO) stimulates differentiation and inhibits p
roliferation and migration of SMCs. Paxillin has been found to play an impo
rtant role in cell differentiation, and its phosphorylation is regulated by
NO in cultured SMCs. However, the regulation of paxillin by NO in the inju
red artery has not been investigated. Therefore, the aim of this study was
to study the effects of in vivo endothelial NO synthase (eNOS) gene transfe
ction on paxillin expression and intimal hyperplasia. A catheter balloon-de
nuded rat carotid artery was transfected in vivo with the replication-defic
ient adenovirus Ad5/RSVeNOS or with Ad5/RSVLacZ as the control. Transfected
eNOS gene expression was determined by immunostaining, Western blot analys
is, and citrulline assay. The expression of paxillin and its associated pro
teins was determined in injured arteries by Western blot analysis. The area
of the intima and the ratio of intima to media were examined on cross sect
ions by morphometry. The data showed that the expression of paxillin was si
gnificantly downregulated after injury. eNOS gene transfer showed no effect
on paxillin downregulation 2 days after injury but significantly enhanced
the recovery of paxillin protein 5 days and 2 weeks after injury. Vinculin,
a paxillin-binding protein, was not altered by vascular injury or by eNOS
gene transfer, eNOS gene transfer significantly inhibited intimal hyperplas
ia for up to 4 weeks. These results suggest that NO inhibition of intimal h
yperplasia may be mediated by enhancing the recovery of injury-caused downr
egulation of paxillin.