期刊文献+

低氧诱导因子-1α诱导分化的骨髓间充质干细胞复合纳米人工骨修复兔桡骨缺损 被引量:3

HIF-1α-induced bone marrow mesenchymal stem cells combined with complex nano-artificial bone repairing rabbit bone defects
下载PDF
导出
摘要 目的探讨低氧诱导因子-1α(hypoxia-inducible factor-1α,HIF-1α)诱导分化的骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs)复合纳米羟基磷灰石(nano-hydroxyapatite,nano-HA)人工骨修复兔桡骨缺损的效果。方法取兔胫骨的骨髓分离培养并鉴定BMSCs;制备携带HIF-1α的慢病毒表达系统,感染BMSCs后与nano-HA共培养得到HIF-1α-e GFP/BMSCs/nano-HA人工骨材料。将30只2月龄新西兰大白兔随机分为3组,每组10只,均通过手术截骨后制成桡骨骨缺损模型,实验组填充HIF-1α-e GFP/BMSCs/nano-HA人工骨材料,对照组填充BMSCs/nano-HA,空白组不填充任何材料。于术后4、8、12周摄X线片观察骨缺损处,并于术后12周获得兔桡骨的大体标本和病理切片,比较桡骨缺损的愈合情况。结果经鉴定,分离培养得到的BMSCs形态良好,高表达CD90、CD105;所有实验动物的桡骨中段缺损模型均构建成功,通过对实验兔的大体标本、X线片及病理切片进行比较分析,实验组和对照组的骨缺损均有所修复,但实验组的新骨形成量更大,骨缺损修复能力优于对照组,空白组骨缺损区未能得到修复。结论 HIF-1α诱导分化的BMSCs与nano-HA复合制成的HIF-1α-e GFP/BMSCs/nano-HA复合人工骨具有良好的骨缺损修复能力,可能成为一种理想的骨缺损修复材料。 Objective To investigate the effect of the artificial bone which composed by hypoxia-inducible factor-1α(HIF-1α)-induced bone marrow mesenchymal stem cells(BMSCs) and nano-hydroxyapatite(nano-HA) in repairing rabbit radius defect. Methods The BMSCs were isolated from the tibia of rabbits, cul-tured and identified. The lentivirus of HIF-1α was prepared and HIF-1α-e GFP/BMSCs/nano-HA artificial bonematerial was produced by co-culturing BMSCs infected with HIF-1α lentivirus and nano-HA. Thirty New Zea-land white rabbits were divided into 3 groups at random. The radial bone defect model was established by surgi-cal osteotomy. The radius defects in experimental group were filled with HIF-1α-e GFP/BMSCs/nano-HA, thosein control group with BMSCs/nano-HA, and those in blank group with nothing. The bone defect was observed at4 th, 8th and 12 th week after operation by X-ray examination, and the healing of radial defect was comparedgrossly and pathologically at 12 th week after operation. Results The BMSCs had good form and high expres-sion of CD90 and CD105. The radial bone defect models were successfully constructed. The bone defects in ex-perimental group and control group healed to some extent, but the new bone formation in the experimental groupwas greater, and the repair ability was better than in the control group. Conclusion The HIF-1α-e GFP/BM-SCs/nano-HA composite artificial bone processes a good ability to repair the bone defect, and is expected to be-come an ideal material for repairing bone defect.
出处 《骨科》 CAS 2016年第3期201-206,212,共7页 ORTHOPAEDICS
基金 深圳市科技研发资金项目(CXZZ20140813160132596,JCYJ20130401112820839)
关键词 低氧诱导因子 间充质干细胞 羟基磷灰石 骨代用品 Hypoxiainducible factor Mesenchymal stem cells Hydroxyapatites Bone substitutes
  • 相关文献

参考文献3

二级参考文献14

  • 1刘晓东,邓廉夫,王君,朱雅萍,魏立.低氧诱导因子-1α对成骨细胞功能的调控作用[J].上海交通大学学报(医学版),2007,27(3):298-302. 被引量:19
  • 21,Prockop D J. Marrow stromal cells as stem cells for nonhematopoietic tissues. Science, 1997,276:71
  • 32,Pittenger MF, Mackay AM, Beck SC et al. Multilineage potentiall of adult human mesenchyma stem cells. Science,1999,284: 143
  • 43,Ferrari G, Cusellade Angelis G, Coletta M et al. Muscle regeneration by bone marrow-derived myogenic progenitors. Science,1998, 279:1528
  • 54,Dexter TM, Allen TD, and Lajtha LG. Conditions controlling the proliferation of hematopoietic stem cells in vitro. J Cell Physiol,1977, 91: 335
  • 65,Bruder SP, Ricalton NS, Boynton RE et al. Mesenchyma stem cell surface antigen SB-10 corresponds to activated leukocyte cell adhesion molecule and is involved in osteogenic differentiation. J Bone Miner Res,1998,13:655
  • 76,Conget PA, Minguell JJ. Phenotypical and functional properties of human bone marrow mesenchyma progenitor cells. J Cell Physiol,1999, 181: 67
  • 87,Fleming JE Jr, Haynesworth SE, Cassiede P et al. Monoclonal antibody against adult marrow-derived mesenchyma stem cells recognizes developing vasculature in embryonic human skin. Dev Dyn,1998,212:119
  • 9陆蕴松,高忠礼,刘光耀.低氧诱导因子-1对血管内皮生长因子的调控[J].中国老年学杂志,2009,29(7):905-907. 被引量:10
  • 10邹多宏,黄远亮.低氧诱导因子-1α的研究进展[J].国际口腔医学杂志,2010,37(3):320-323. 被引量:24

共引文献65

同被引文献22

引证文献3

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部