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机构地区:[1]中国医科大学第二临床学院骨科,沈阳110004 [2]中国医科大学第一临床学院骨科,沈阳110004
出 处:《中华实验外科杂志》2007年第4期471-472,共2页Chinese Journal of Experimental Surgery
基 金:中国博士后科研基金(20060390974)
摘 要:目的观察核心结合因子a1(Cbfal)基因转染的人骨髓基质干细胞(hBMSCs)复合生物衍生骨支架异位成骨的效果。方法雌性BALB/C裸鼠18只,随机分为3组:转染Cbfa1基因的hBMSCs复合支架(A)、未转染细胞复合支架(B)和单纯支架组(C),每组6只。分别将各组人工骨植入裸鼠背部皮下,于术后4、8周行组织学、免疫组织化学和荧光原位杂交等检测。结果Cbfal基因转染后,可诱导BMSCs骨钙素、Ⅰ型胶原呈阳性表达。体内植入后,A组成骨速度及成骨质量均明显优于其他组;植入细胞及宿主间质细胞呈骨钙素、骨形态发生蛋白2阳性表达;4周时,Y染色体阳性细胞数明显高于B组。结论Cbfa1基因转染BMSCs,能够诱导其向成骨细胞分化、上调骨形态发生蛋白2基因表达并提高移植细胞的生存率,明显促进异位成骨能力。Objective To evaluate the osteogenetic potential of human mesenchymal stem cells (hMSCs) transfected with core-binding factor al (Cbfal) gene. Methods hBMSCs transfected with Cbfal gene were seeded on allogenetic bone scaffold to construct tissue engineering bone. The composite ( group A) then were implanted subcutaneously into the back of the nude mice. Two control groups were set up in the experiment: composite of untransfected MSCs and scaffold ( group B) and only scaffolds (group C). Histological examination, immunohistochemical staining and fluorescent in situ hybridization were conducted after 4 and 8 weeks. Results Cbfal gene transfection could induce MSCs' positive expression of osteocalcin and type Ⅰ collagen. After implantation in vivo,the speed and quality of bone formation in group A were much better than those in other groups. Both transplanted ceils and mesenchymal cells displayed the positive expression of osteocalcin and BMP-2;At 4th week, the number of Y chromosome positive cells was obviously more than that in group B. Conclusion Cbfal gene transfection can induce differentiation of BMSCs into osteoblast, up-regulate its BMP-2 gene expression and enhance survival rate of implanted cells,can obviously promote osteogenenic potential of BMSCs in eetopia.
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