Abstract | BACKGROUND: To investigate the molecular mechanism of autologous venous graft intimal hyperplasia, a mouse model is needed. Currently only vein to carotid artery mouse models are available and are hampered by a high thrombosis rate. We hypothesized that operating on the aorta would lead to intimal hyperplasia with decreased risk of thrombosis. MATERIALS AND METHODS: In C57BL/6J mice, the left external jugular vein was grafted into the infrarenal abdominal aorta by end-to-end anastomosis with 11-0 Ethilon. Grafts harvested at 1, 2, 4, 8, and 16 weeks postoperatively were subjected to histological and immunohistochemical analysis. RESULTS: Thirty-one of 35 mice survived; 2 mice were sacrificed secondary to thrombosis. The percentage lumen narrowing (+/-SE) was 7.8 +/- 0.3, 16.4 +/- 0.9, 19.2 +/- 0.9, 22.3 +/- 0.8, and 23.9 +/- 1.6% at 1, 2, 4, 8 and 16 weeks, respectively. Nuclear density decreased with each successive time point. The percentage of alpha-smooth-muscle actin-positive cells within the neointima peaked at 16 weeks (53%), and the percentage of cells positive for proliferating cell nuclear antigen peaked at 2 weeks (39%). CONCLUSIONS: We thus report on a novel mouse model of intimal hyperplasia in autologous venous grafts with a low thrombosis rate. Further studies using this model, coupled with genetic and bone marrow transplantation mouse models, should lead to significant enhancement in understanding of the mechanism of intimal hyperplasia.
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Authors | Yanpeng Diao, Jing Xue, Mark S Segal |
Journal | The Journal of surgical research
(J Surg Res)
Vol. 126
Issue 1
Pg. 106-13
(Jun 01 2005)
ISSN: 0022-4804 [Print] United States |
PMID | 15916983
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Proliferating Cell Nuclear Antigen
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Topics |
- Animals
- Cell Proliferation
- Disease Models, Animal
- Hyperplasia
- Jugular Veins
(transplantation)
- Male
- Mice
- Mice, Inbred C57BL
- Muscle, Smooth, Vascular
(pathology)
- Proliferating Cell Nuclear Antigen
(analysis)
- Transplantation, Autologous
- Tunica Intima
(pathology)
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