Experimental study of core binding factor a1 gene-modified rabbit skin fibroblasts enhance bone defect repair.
- Author:
De-chang XIAO
1
;
Lian-fu DENG
;
Qing-ming YANG
;
Yan-bin TAN
;
Xue-min LÜ
;
Wei ZHANG
;
Wei FENG
;
Ya-feng HE
;
Jing LIANG
;
Ya-ping ZHU
;
Jin QI
;
Qi ZHOU
;
Jun WANG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Bone Regeneration; Bone Substitutes; Bone Transplantation; Cells, Cultured; Core Binding Factor Alpha 1 Subunit; genetics; Disease Models, Animal; Fibroblasts; cytology; metabolism; Plasmids; genetics; Rabbits; Radius; injuries; physiopathology; surgery; Random Allocation; Skin; cytology; Tissue Engineering; methods; Transfection
- From: Chinese Journal of Surgery 2007;45(22):1565-1568
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate bone defect healing by true bone ceramic complex carrying core binding factor a1 (Cbfa1) gene modified rabbit skin fibroblasts.
METHODSTransfect rabbit skin fibroblasts (RSF) with both eukaryotic expression vector pSG5 which could express Cbfa1 gene and pSG5. After being cultured for 48 h, the transfected RSF were seeded into true bone ceramic (TBC) of 2 cm in length and 4 mm in diameter to construct pSG5-Cbfa1/RSF/TBC complex and pSG5/RSF/TBC complex. Forty-eight bone defect model rabbits were randomized into four groups, each has 6 rabbits (12 radius), due to different treatment. group I: with pSG5-Cbfa1/RSF/TBC complex, group II: with pSG5/RSF/TBC complex, group III: with TBC, Group IV: empty control. After being seeded and cultured for about 24 h the complexes were implanted into 2 cm long bone defects in the middle of bilateral radius of rabbits. The radius were inspected by X-ray and then the specimens were collected at the end of the fourth and twelfth weeks after operation. Then, the specimens were decalcified and histologically investigated with Hematoxylin eosin staining and Masson staining methods. Newly synthesized trabecular bone was inspected by image analysis system and the strength of bone defect area treated with graft-implantation was tested with biomechanical method-three point bending test.
RESULTSIn group I, trabecular bone was actively synthesized to generate a great amount of trabecular bone and osteon. Preliminary union and bone defect healing were completed with good biomechanical characteristics. There were no newly synthesized trabecular in the other three groups, and bone defect healing were not discovered. The amount of newly synthesized trabecular bone and the results of biomechanical testing differed significantly between group I and the other three (P < 0.01). The efficacy of group I was significantly better than that of the other three groups.
CONCLUSIONTrue bone ceramic complex composed with Cbfa1 gene modified rabbit skin fibroblasts can effectively heal bone defect in rabbits.
