Study for the Ureteral Reconstruction with Tissue Engineering Using Poly (glycolide/epsilon-caprolactone) Scaffold-1.
- Author:
Jong Yoon BAHK
1
;
Jae Seog HYUN
;
Myeong Ok KIM
;
Il Keun KWON
;
Ki Dong PARK
;
Young Ha KIM
Author Information
1. Department of Urology, Medical College, College of Natural Science, Gyeongsang National University.
- Publication Type:In Vitro ; Original Article
- Keywords:
Primary culture;
Tissue engineering;
Dynamic culture;
Scaffold
- MeSH:
3T3 Cells;
Adult;
Animals;
Artificial Organs;
Cadaver;
Cells, Cultured;
Dogs;
Enzyme-Linked Immunosorbent Assay;
Female;
Fibroblasts;
Humans;
Male;
Mice;
Muscle Cells;
Myocytes, Smooth Muscle;
Porifera;
Tissue Engineering*;
United Nations;
Ureter*;
Urinary Bladder
- From:Korean Journal of Urology
2001;42(4):371-378
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Transplantation is one modality saving human life. But not only lack of the living or cadaveric human organs but also immunologic problems or some ethical situations limit transplantation in terminal stage patients. Recent research for escaping from those problems resulted in the reconstruction of the artificial organ using patients' own cells with tissue engineering. The goal of this study is, for the better reconstruction of urinary system using tissue engineering, to perform basic researches on techniques related with seeding and viability of cells. MATERIALS AND METHODS: We used 16 adult dogs, 4 female and 12 male, for primary culture of the dog bladder mucosal cell and muscle cell. The scaffold we used was made of absorbable substance polyglycolide/epsilon-caprolactone (GL/CL) in thin sponge like shape. Fibroblast 3T3 cell was used for control and 16 primary cultured mucosal cell and smooth muscle cells were used. For dynamic culture, rocker was adapted with for 5 hours. Attached cells were evaluated by 562nm ELISA reader using BCA method and scanning electron microscope. RESULTS: Successful primary culture was achieved with cells from dog bladder, and results were much better by using male dog. The dynamic culture increased attachment of the cell in scaffold and the cell attached at deeper portion of the scaffold. Long term culture showed formation of the cellular sheets on the surface of scaffold preventing inner passage of the suggesting disadvantageous condition for cells in core of the scaffold. CONCLUSIONS: We conclude that for the better attachment of the cultured cells on scaffolds, dynamic culture would be desirable. And for the better in vivo reconstruction of the organ with primary cultured cell attached scaffold, evaluation of culture state with repeated in vitro experiments are necessary.
