Title | Adenovirus-mediated expression of a truncated PDGFbeta receptor inhibits thrombosis and neointima formation in an avian arterial injury model. |
Publication Type | Journal Article |
Year of Publication | 2001 |
Authors | Ding H, Wang R, Marcel R, Fisher DZ |
Journal | Thromb Haemost |
Volume | 86 |
Issue | 3 |
Pagination | 914-22 |
Date Published | 2001 Sep |
ISSN | 0340-6245 |
Keywords | Animals, Aviadenovirus, Catheterization, Cell Division, Cell Movement, Chickens, Femoral Artery, Genetic Therapy, Genetic Vectors, Hyperplasia, Male, Muscle, Smooth, Vascular, Phosphorylation, Platelet-Derived Growth Factor, Protein Processing, Post-Translational, Proto-Oncogene Proteins c-sis, Receptor, Platelet-Derived Growth Factor beta, Recombinant Fusion Proteins, Thrombosis, Tunica Intima |
Abstract | Platelet-derived growth factor (PDGF) is a major mediator of neointima formation after arterial injury. We constructed a recombinant adenovirus, Ad/PDGFtr, that expresses the soluble extracellular domain of the murine PDGFbeta receptor (PDGFtr). The expressed PDGFtr was appropriately glycosylated and secreted by chicken vascular smooth muscle cells (SMCs) in vitro. The expressed PDGFtr inhibited human PDGF-BB induced receptor autophosphorylation, and also inhibited PDGF-BB induced cell proliferation without affecting PDGF-AA induced mitogenesis. In vivo transduction of balloon-injured rooster femoral arteries with Ad/PDGFtr resulted in expression and secretion of the glycosylated PDGFtr. The expressed PDGFtr significantly inhibited neointima formation compared with controls. Neointima-associated thrombus was significantly reduced in Ad/PDGFtr transduced arteries compared with controls. Thus, in addition to impacting on SMC proliferation and migration, PDGF-BB plays a role in thrombus formation in response to arterial injury. Growth factor inhibition by localized gene delivery constitutes a powerful approach to intervene in the molecular pathways involved in vascular disease. |
Alternate Journal | Thromb. Haemost. |
PubMed ID | 11583327 |
Grant List | HL03113 / HL / NHLBI NIH HHS / United States |
Submitted by kej2006 on June 6, 2018 - 4:10pm