The Decellularized Vascular Allograft as an Experimental Platform for Developing a Biocompatible Small-Diameter Graft Conduit in a Rat Surgical Model.
10.3349/ymj.2011.52.2.227
- Author:
Seong Jun HWANG
1
;
Seong Who KIM
;
Suk Jung CHOO
;
Byoung Wook LEE
;
I rang IM
;
Hye Joo YUN
;
Sang Kwon LEE
;
Hyun SONG
;
Won Chul CHO
;
Jae Won LEE
Author Information
1. Department of Anatomy and Cell Biology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Tissue engineering;
vessel;
rat;
animal model
- MeSH:
Animals;
Aorta, Abdominal/anatomy & histology/cytology/*surgery;
Biocompatible Materials/*therapeutic use;
*Disease Models, Animal;
Female;
Graft Survival/immunology;
Rats;
Rats, Sprague-Dawley;
Tissue Engineering/*methods;
Transplantation, Homologous/*methods
- From:Yonsei Medical Journal
2011;52(2):227-233
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: The present study was aimed to assess the feasibility of using decellularized aortic allograft in a rat small animal surgical model for conducting small diameter vascular tissue engineering research. MATERIALS AND METHODS: Decellularized aortic allografts were infra-renally implanted in 12 Sprague-Dawley (SD) adult rats. The conduits were harvested at 2 (n = 6) and 8 weeks (n = 6), and assessed by hematoxylin and eosin (H&E), van Gieson, Masson Trichrome staining, and immunohistochemistry for von Willebrand factor, CD 31+, and actin. RESULTS: Consistent, predictable, and reproducible results were produced by means of a standardized surgical procedure. All animals survived without major complications. Inflammatory immune reaction was minimal, and there was no evidence of aneurysmal degeneration or rupture of the decellularized vascular implants. However, the aortic wall appeared thinner and the elastic fibers in the medial layer showed decreased undulation compared to the normal aorta. There was also minimal cellular repopulation of the vascular media. The remodeling appeared progressive from 2 to 8 weeks with increased intimal thickening and accumulation of both collagen and cells staining for actin. Although the endothelial like cells appeared largely confluent at 8 weeks, they were not as concentrated in appearance as in the normal aorta. CONCLUSION: The results showed the present rat animal model using decellularized vascular allograft implants to be a potentially durable and effective experimental platform for conducting further research on small diameter vascular tissue engineering.
