疏水蛋白HFBI及胶原共修饰的PLGA对神经干细胞贴附和生长的影响  被引量:1

The Effect of PLGA Modified by Hydrophobin HFBI and Collagen TypeⅠ on the Adhesion and Growth of Neural Stem Cells in Vitro

在线阅读下载全文

作  者:於永[1] 李兰英[2] 马景鑑[1] 侯森[3] 李新新[3] 冯喜增[3] 

机构地区:[1]天津医科大学总医院神经外科,300052 [2]天津医科大学内分泌研究所,卫生部及天津市激素与发育重点实验室 [3]南开大学生命科学学院生物活性材料教育部重点实验室

出  处:《天津医药》2009年第6期498-500,I0003,共4页Tianjin Medical Journal

基  金:天津市应用基础研究计划项目(项目编号:07JCYBJC10100)

摘  要:目的:探讨神经干细胞(NSCs)在经疏水蛋白HFBI和Ⅰ型胶原联合修饰的聚乳酸-乙醇酸(PLGA)膜上贴附和生长的可行性。方法:将神经干细胞分离、纯化及扩增后,在无血清和有血清的条件下,分别接种到PLGA膜和经疏水蛋白HFBI和Ⅰ型胶原联合修饰的PLGA膜上,观察神经干细胞的贴附、生长情况。结果:经过培养,无血清组中,在PLGA膜上没有观察到神经干细胞;在疏水蛋白HFBI与胶原联合修饰的PLGA膜上,观察到有少量的神经干细胞呈圆形状贴附,生长。血清组中,在PLGA膜以及疏水蛋白HFBI和胶原联合修饰的PLGA膜上,均观察到存在大量细胞生长,并且在疏水蛋白HFBI和胶原联合修饰的PLGA膜上,观察到更多含有突起的细胞。结论:疏水蛋白HFBI和Ⅰ型胶原联合修饰PLGA膜有利于促进神经干细胞贴壁,在血清的条件下明显促进神经干细胞生长和分化。Objective: To investigate the adhesion and growth of neural stem cells (NSCs) on the native PLGA which was modified by hydrophobin HFBI and collagen type Ⅰ. Methods: NSCs were cultured on the native PLGA, which was modified by hydrophobin HFBI and collagen type Ⅰ, with or without serum, respectively. The adhesion and growth of NSCs were observed. Results: In the medium without serum, no NSCs adhered to the surface of PLGA and only a few cells adhered to and grew on the surface of PLGA modified by hydrophobin HFBI and collagen. In the medium supplemented with serum, most cells adhered to and grew on the surface of both PLGA and PLGA modified by hydrophobin HFBI and collagen. Besides, more cells with cellular processes were observed on the PLGA substrate modified by hydrophobin HFBI and Collagen. Conclusion: The PLGA modified by hydrophobin HFBI and collagen typeⅠ modifying PLGA was demonstrated to promote the adhesion and growth of NSCs. The NSCs could differentiate at the presence of serum.

关 键 词:干细胞 神经系统 细胞 培养的 聚乙醇酸 胶原Ⅰ型 真菌蛋白质类 大鼠 WISTAR 

分 类 号:R318.08[医药卫生—生物医学工程] R329.2[医药卫生—基础医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象