摘要
应用自行设计的RGD接枝的聚(羟基乙酸-L-赖氨酸-乳酸),复合聚乳酸、b-磷酸三钙和神经生长因子(NGF)制备神经导管材料(PNGF)。在体外制备材料浸提液,与PC12细胞共培养1 d、2 d和3 d,分别提取总RNA,通过实时定量PCR试验方法,观察PC12细胞GAP43和β-TubulinⅡ基因表达的变化。结果显示GAP43和β-TubulinⅡ基因的表达量明显高于对照组,其峰值出现在第二天。材料浸提液中NGF在诱导PC12细胞分化中起到显著作用。
A novel nerve guidance conduit(NGC) was synthesized by embedding nerve growth factor(NGF) into a degradable RGD-modified composite(PRGD) to improve the peripheral nerve repair(PNGF).This study was to evaluate the responses of GAP43 and β-Tubulin Ⅱgenes mRNA expression when PC12 cells were exposed to the extract of PNGF films.RNA was isolated from PC12 cells cultured in vitro and gene expression were detected by real-time quantitative PCR at 1 d,2 d and 3 d.Results indicated that the transcription of GAP43 and β-Tubulin Ⅱgenes were significantly up-regulation in the extract of PNGF films and the peak were almost presented at the second day.Results show that the sustained released NGF promoted PC12 cells differentiation.
出处
《武汉理工大学学报》
CAS
CSCD
北大核心
2011年第5期59-62,共4页
Journal of Wuhan University of Technology
基金
中央高校基本科研业务费专项资金(2010-ZY-CL-025)