碱性成纤维细胞生长因子复合脱细胞骨基质/壳聚糖支架修复骨缺损  

Acellular bone matrix/chitosan scaffold combined with basic fibroblast growth factor for repairing bone defects

作　　者：张志文[1] 黄玉良[1] 张理选[2] 王晓锋[1] 陈锐雄[1] Zhang Zhiwen;Huang Yuliang;Zhang Lixuan;Wang Xiaofeng;Chen Ruixiong(Department of Trauma and Orthopedics,Huizhou Central People’s Hospital,Huizhou 516001,Guangdong Province,China;Department of Joint Surgery,Huizhou Central People’s Hospital,Huizhou 516001,Guangdong Province,China)

机构地区：[1]惠州市中心人民医院创伤骨科,广东省惠州市516001 [2]惠州市中心人民医院关节外科,广东省惠州市516001

出　　处：《中国组织工程研究》2021年第34期5439-5444,共6页Chinese Journal of Tissue Engineering Research

基　　金：广东省医学科研基金立项项目(B2019140),项目负责人:张理选。

摘　　要：背景:有研究显示,碱性成纤维细胞生长因子可促进间充质干细胞的增殖与成骨分化。目的:对比脱细胞骨基质/壳聚糖支架复合碱性成纤维细胞生长因子前后修复兔股骨缺损的能力。方法:采用融合共混与冷冻干燥法制备脱细胞骨基质/壳聚糖支架,采用浸渍法制备碱性成纤维细胞生长因子/脱细胞骨基质/壳聚糖支架。将小鼠胚胎成骨细胞MC3T3-E1分别接种于两种支架表面,以单独培养的细胞为对照,进行细胞增殖、细胞黏附与成骨基因检测。在36只6月龄新西兰大白兔双侧股骨远端制备直径5 mm的骨缺损模型,抽签法随机分3组,空白组不进行任何干预,单纯复合支架组、生长因子+复合支架组分别植入脱细胞骨基质/壳聚糖支架与碱性成纤维细胞生长因子/脱细胞骨基质/壳聚糖支架,进行骨缺损部位X射线片与组织学检查。结果与结论:①在培养的1-11 d内,碱性成纤维细胞生长因子/脱细胞骨基质/壳聚糖支架组的细胞增殖快于脱细胞骨基质/壳聚糖支架组(P<0.05),脱细胞骨基质/壳聚糖支架组快于对照组(P<0.05);②细胞与支架共培养4 d后,碱性成纤维细胞生长因子/脱细胞骨基质/壳聚糖支架组培养4,7 d的成骨基因Ⅰ型胶原、骨钙素、骨桥蛋白及Runx2 mRNA表达均高于脱细胞骨基质/壳聚糖支架组(P<0.05),培养7 d后的碱性磷酸酶mRNA表达高于脱细胞骨基质/壳聚糖支架组(P<0.05);③共培养7 d后的扫描电镜显示,两组支架均支持MC3T3-E1细胞的黏附;④动物实验X射线片显示,空白组术后12周时无明显的骨修复;单纯复合支架组术后8周时可见新骨生成,术后12周时可见明显新骨生成;细胞因子+复合支架组术后4周时即可见新骨生成,至术后12周时骨缺损部位几乎完全修复;⑤动物实验术后12周的缺损部位苏木精染色与Masson染色显示,空白组可见大量的纤维组织;两支架组可见大量的新骨生成,其中生长因�BACKGROUND:Some studies have shown that basic fibroblast growth factor can promote the proliferation and osteogenic differentiation of mesenchymal stem cells.OBJECTIVE:To compare the ability of acellular bone matrix/chitosan scaffold combined with basic fibroblast growth factor in repairing rabbit femoral defect.METHODS:The acellular bone matrix/chitosan scaffolds were prepared by fusion blending and freeze-drying method,and the acellular bone matrix/chitosan scaffold loaded with basic fibroblast growth factor was prepared by immersion method.Mouse embryonic osteoblasts MC3T3-E1 were seeded on the surface of the two scaffolds for cell proliferation,cell adhesion and osteogenic gene detection.Cells cultured alone served as control.Bone defect models with a diameter of 5 mm were made in bilateral distal femurs using thirty-six 6-month-old New Zealand white rabbits and randomly divided into three groups by drawing lots.The blank group was not intervened.The simple composite scaffold and growth factor+composite scaffold groups were implanted with acellular bone matrix/chitosan scaffold and acellular bone matrix/chitosan scaffold loaded with basic fibroblast growth factor for X-ray and histological examination.RESULTS AND CONCLUSION:(1)Within 1-11 days of culture,the cell proliferation of basic fibroblast growth factor/acellular bone matrix/chitosan scaffold group was faster than that of the acellular bone matrix/chitosan scaffold group(P<0.05),and that of the acellular bone matrix/chitosan scaffold group was faster than that of the control group(P<0.05).(2)After 4 days of co-culture with the scaffold,the mRNA expressions of type I collagen,osteocalcin,osteopontin and Runx2 were higher in the cells in basic fibroblast growth factor/acellular bone matrix/chitosan scaffold group cultured for 4 and 7 days than those of acellular bone matrix/chitosan scaffold group(P<0.05),and the mRNA expression of alkaline phosphatase was higher than that of acellular bone matrix/chitosan scaffold group after 7 days of culture(P<0.05).(

关 键 词：碱性成纤维细胞生长因子 壳聚糖 支架 脱细胞骨基质 复合支架 股骨缺损修复 

分 类 号：R459.9[医药卫生—治疗学] R318.08[医药卫生—临床医学]