中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2013年
8期
1362-1366
,共5页
宗海斌%贾金领%董玉珍%周慧聪
宗海斌%賈金領%董玉珍%週慧聰
종해빈%가금령%동옥진%주혜총
生物材料%纳米生物材料%基因工程%纳米微球载体%神经营养因子 3%许旺细胞%神经缺损%省级基金%生物材料图片文章
生物材料%納米生物材料%基因工程%納米微毬載體%神經營養因子 3%許旺細胞%神經缺損%省級基金%生物材料圖片文章
생물재료%납미생물재료%기인공정%납미미구재체%신경영양인자 3%허왕세포%신경결손%성급기금%생물재료도편문장
biomaterials%nano-biomaterials%genetic engineering%nanoparticle carrier%neurotrophic factor-3%Schwann cells%nerve defects%provincial grants-supported paper%biomaterial photographs-containing paper
背景:纳米微球基因转染技术携带或增强种植细胞可持续稳定延长其释放,保持其活性和作用时间.目的:观察纳米微球载体转染神经营养因子3基因修饰的许旺细胞对坐骨神经缺损的促进和修复作用.方法:采用纳米微球载体将神经营养因子3基因转染入体外培养的新生 Wistar 大鼠许旺细胞.取 Wistar成年大鼠80只制作坐骨神经缺损模型,将4种不同的移植物注入细胞外基质凝胶-聚乳酸聚羟基乙酸共聚物管桥接管内:空白对照组未注入其他任何物质,细胞组注入许旺细胞,基因组注入神经营养因子3基因,实验组注入神经营养因子3基因修饰的许旺细胞.结果与结论:术后坐骨神经及肌纤维横截面积染色比较,实验组优于细胞组、基因组(P <0.01),细胞组、基因组均优于空白对照组(P <0.01),细胞组、基因组组间比较差异无显著性意义(P >0.05).表明神经营养因子3基因转染许旺细胞移植,可相互促进,再造神经再生的微环境,促进并修复缺损坐骨神经缺损.
揹景:納米微毬基因轉染技術攜帶或增彊種植細胞可持續穩定延長其釋放,保持其活性和作用時間.目的:觀察納米微毬載體轉染神經營養因子3基因脩飾的許旺細胞對坐骨神經缺損的促進和脩複作用.方法:採用納米微毬載體將神經營養因子3基因轉染入體外培養的新生 Wistar 大鼠許旺細胞.取 Wistar成年大鼠80隻製作坐骨神經缺損模型,將4種不同的移植物註入細胞外基質凝膠-聚乳痠聚羥基乙痠共聚物管橋接管內:空白對照組未註入其他任何物質,細胞組註入許旺細胞,基因組註入神經營養因子3基因,實驗組註入神經營養因子3基因脩飾的許旺細胞.結果與結論:術後坐骨神經及肌纖維橫截麵積染色比較,實驗組優于細胞組、基因組(P <0.01),細胞組、基因組均優于空白對照組(P <0.01),細胞組、基因組組間比較差異無顯著性意義(P >0.05).錶明神經營養因子3基因轉染許旺細胞移植,可相互促進,再造神經再生的微環境,促進併脩複缺損坐骨神經缺損.
배경:납미미구기인전염기술휴대혹증강충식세포가지속은정연장기석방,보지기활성화작용시간.목적:관찰납미미구재체전염신경영양인자3기인수식적허왕세포대좌골신경결손적촉진화수복작용.방법:채용납미미구재체장신경영양인자3기인전염입체외배양적신생 Wistar 대서허왕세포.취 Wistar성년대서80지제작좌골신경결손모형,장4충불동적이식물주입세포외기질응효-취유산취간기을산공취물관교접관내:공백대조조미주입기타임하물질,세포조주입허왕세포,기인조주입신경영양인자3기인,실험조주입신경영양인자3기인수식적허왕세포.결과여결론:술후좌골신경급기섬유횡절면적염색비교,실험조우우세포조、기인조(P <0.01),세포조、기인조균우우공백대조조(P <0.01),세포조、기인조조간비교차이무현저성의의(P >0.05).표명신경영양인자3기인전염허왕세포이식,가상호촉진,재조신경재생적미배경,촉진병수복결손좌골신경결손.
@@@@BACKGROUND: The technology of nanoparticle carrier transferring gene can carry or enhance plant cellsustainable stability, extend its release and maintain its activity and duration. OBJECTIVE: To explore the effects of nanoparticle carrier with neurotrophic factor-3 on transfection of Schwann cells in facilitating and repairing sciatic nerve defects.METHODS: The neurotrophic factor-3 genes were transfected to the Schwann cells of newborn Wistar rats with nanoparticle carrier. Eighty adult Wistar rats were selected to make the sciatic nerve defect model. Then four kinds of grafts were injected into the pipe bridge takeover of extracel ular matrix gel-poly( lactide-co-glycolide): the blank control group was not injected with other substances, the cel group was injected with Schwann cells, the gene group was injected with neurotrophic factor-3 gene, and the experimental group was injected with neurotrophic factor-3 gene modified Schwann cells. RESULTS AND CONCLUSION: The staining of sciatic nerve and muscle fiber cross-sectional area was better in the experimental group than in the cel group and gene group (P < 0.01), which was better in the cel and gene groups than the blank control group (P < 0.01); but, there was no significant difference between the cel group and gene group (P > 0.05). It indicated that neurotrophic factor-3 gene modified Schwann cells transplantation can reconstruct the microenvironment of nerve regeneration and promote repair of sciatic nerve defects.