Article
In vivo suppression of vein graft disease by nonviral, electroporation-mediated, gene transfer of tissue inhibitor of metalloproteinase-1 linked to the amino terminal fragment of urokinase (TIMP-1.ATF), a cell-surface directed matrix metalloproteinase inhibitor.
Journal of vascular surgery - 1 Feb 2010
Eefting Daniel, de Vries Margreet R, Grimbergen Jos M, Karper Jacco C, van Bockel J Hajo, Quax Paul H A
Abstract excerpt
BACKGROUND: Smooth muscle cell (SMC) migration and proliferation are important in the development of intimal hyperplasia, the major cause of vein graft failure. Proteases of the plasminogen activator (PA) system and of the matrix metalloproteinase (MMP) system are pivotal in extracellular matrix degradation and, by that, SMC migration. Previously, we demonstrated that inhibition of both protease systems...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
