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J Zhejiang Univ Sci B ; 15(5): 482-90, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24793766

RESUMO

This study was designed to investigate the effects of local delivery of adipose-derived stem cells (ADSCs) transfected with transcription factor osterix (OSX) on bone formation during distraction osteogenesis. New Zealand white rabbits (n=54) were randomly divided into three groups (18 rabbits per group). A directed cloning technique was used for the construction of recombinant plasmid pEGFP-OSX, where EGFP is the enhanced green fluorescence protein. After osteodistraction of the right mandible of all experimental rabbits, rabbits in group A were treated with ADSCs transfected with pEGFP-OSX, group B with ADSCs transfected with pEGFP-N1, and group C with physiological saline. Radiographic and histological examinations were processed after half of the animals within each group were humanely killed by injection of sodium pentothal at Week 2 or 6 after surgery. The distraction bone density was measured as its projectional bone mineral density (BMD). Three parameters were measured, namely, the thickness of new trabeculae (TNT), and the volumes of the newly generated cortical bone (NBV1) and the cancellous bone (NBV2) of the distracted regions. Good bone generation in the distraction areas was found in group A, which had the highest BMD, TNT, and NBV in the distraction zones among the groups. There was no significant difference in bone generation in the distraction areas between groups B and C. The results indicate that the transplantation of ADSCs transfected with pEGFP-OSX can effectively promote bone generation during distraction in vivo.


Assuntos
Proteínas de Fluorescência Verde/genética , Mandíbula/crescimento & desenvolvimento , Osteogênese por Distração/métodos , Osteogênese/fisiologia , Transplante de Células-Tronco/métodos , Células-Tronco/fisiologia , Fatores de Transcrição/genética , Adipócitos/citologia , Adipócitos/metabolismo , Animais , Diferenciação Celular , Células Cultivadas , Terapia Combinada , Terapia Genética/métodos , Humanos , Masculino , Coelhos , Fator de Transcrição Sp7 , Células-Tronco/citologia , Transfecção/métodos , Resultado do Tratamento
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