Regeneration of autologous tissue-engineered cartilage by using basic-fibroblast growth factor in vitro culture.
- Author:
Xiao-bang DING
1
;
Ning-xin CHENG
;
Bing CHEN
;
Wan-yao XIA
;
Lei CUI
;
Wei LIU
;
Yi-lin CAO
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cartilage; cytology; drug effects; physiology; Cell Division; drug effects; Cells, Cultured; Chondrocytes; cytology; drug effects; Female; Fibroblast Growth Factors; pharmacology; physiology; Male; Regeneration; drug effects; Swine; Tissue Engineering; methods; Transplantation, Autologous
- From: Chinese Journal of Plastic Surgery 2004;20(3):215-218
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effect of the basic fibroblast growth factor (b-FGF) to regenerate an autologous tissue-engineered cartilage in vitro.
METHODSThe Cells were harvested from the elastic auricular cartilage of swine,and were plated at the concentration of 1 x 10(4) cells/cm2 , studied in vitro at two different media enviroments: Group I contained Ham's F-12 with supplements and b-FGF, Group II contained Ham's F-12 only with supplements. The passage 2 cells (after 12.75 +/- 1.26 days) were harvested and mixed with 30% pluronic F-127/Ham's F-12 at the concentration of 50 x 10(6) cells/ml. It was injected subcutaneously at 0.5 ml per implant. The implants were harvested 8 weeks after the vivo culture and examined with the histological stains.
RESULTSThe chondrocytes displayed morphologically similar to the fibroblasts in the media containing basic-FGF. The number of cell doublings (after 12.75 +/- 1.26 days) in vitro culture was as the following: Group I, 70; Group II, 5.4. Eight 8 weeks after the vivo autologous implantation, the average weight (g) and volume (cm3) in each group was as the following: Group I, 0.371 g/0.370 cm3 Group II, 0.179 g/0.173 cm3 (P < 0.01). With the b-FGF in vitro culture, the cells were expanded by 70 times after 2 weeks. Histologically, all of the engineered cartilage in the two groups were similar to the native elastic cartilage.
CONCLUSIONThese results indicate that the basic-FGF could be used positively to enhance the quality and quantity of the seeding cells for the generation of the well-engineered cartilage.