期刊文献+

骨形态发生蛋白-2治疗股骨头坏死研究进展

Advances in bone morphogenetic protein 2 in treatment of femoral head necrosis
下载PDF
导出
摘要 随着细胞组织工程学的发展,骨形态发生蛋白(bone morphogenetic protein,BMP)越来越多的应用在骨科领域,而骨形态发生蛋白-2(bone morphogenetic protein,BMP-2)在治疗骨缺损,骨不愈合等方面的效果已经在基础实验和临床实践上均得到了证实[1-3],其作用机制可能是BMP-2可诱导间充质干细胞向软骨方向分化,并通过Smad通路及MAPK通路传导,并对骨组织的形成、生长和损伤的修复具有促进作用[4]。基于这一作用机制,越来越多的学者把研究重点放在治疗股骨头坏死领域,文章就近年来BMP-2治疗股骨头坏死研究进展。 With the development of tissue engineering, bone morphogenetic protein (bone morphogenetic protein, BMP) applications study is becoming more and more widely in the field of orthopedics,The therapeutic effect of bone morphogenetic protein-2 (bone morphogenetic protein, BMP-2) including bone defects,nonunion and other aspects have been demonstrated on the basis of experimental and clinical practice[1-3],Its mechanism may be BMP-2 can induce differentiation of mesenchymal stem cells into cartilage direction,conduct through Smad pathway and MAPK pathway,and promote bone formation , tissue growth and damage repair[4]. Based on this mechanism of action, more and more scholars have putted study focuses on the field of femoral head necrosis treatment, this article makes a brief summary of the treatment of femoral head necrosis advances of BMP-2 in recent years.
出处 《大众科技》 2014年第12期95-97,共3页 Popular Science & Technology
关键词 骨形态发生蛋白 股骨头坏死 组织工程 Bone morphogenetic protein femoral head necrosis tissue engineering
  • 相关文献

参考文献26

  • 1Riley EH, Lane JM,Urist MR,et al. Bone morphogenetic protein-2: biology and applications[J].Clin Orthop Relat Res, 1996, (324) :39- 46. 被引量:1
  • 2Boden SD,Kang J,Sandhu HS,et al. Use of recombinant bone morphogenetic protein-2 to achieve posterolateral lumbar spine fusion in humans:a prospective randomized chnical pilot trial: 2002 Volvo Award in clinical studies[J]. Spine,2002,27:2662-2673. 被引量:1
  • 3Yoshito Katayama, Yukihiro Matsuyama, Hisatake oshihara,et al.Clinical and radiographic outcomes of posterolateral lumbar spine fiasion in humans using recombinant human bone morphogenetic protein-2: an average five-year follow-up study[J]. Int Orthop. 2009,33(4):1061-1067. 被引量:1
  • 4谢在春,郭卫真,卢东荣,刘妮,庞志宇,于永春.BMP2诱导C3H10T1/2细胞成软骨分化的分子机制研究[J].广州医学院学报,2012,40(2):11-15. 被引量:6
  • 5Urist MR. Bone: formation by autoinduction[J]. Science, 1965,(150):893-899. 被引量:1
  • 6Wozeney JM, Rosen V, Celeste AJ, et al. Novel regulators of bone formation: molecular clones and activities[J]. Science, 1988, (242): 1528 - 1534. 被引量:1
  • 7张斌,陈苏民.人骨形成蛋白-2的结构与生物学活性[J].国外医学(分子生物学分册),2001,23(6):360-362. 被引量:2
  • 8Kakudo N, Kusumotok,Wang YB, et al.Immunolocalization of vascular endothelial growth factor on intramuscular ectopic osteoinduction by bone morphogenetic protein-2[J]. Life Sci, 2006,79(19):1847-1855. 被引量:1
  • 9Nohe A, Keating E, UnderhillT M, et al. Effect of the d istribution and clustering of the type I A BMP receptor (ALK3) with the type Ⅱ BMP receptor on the activation of signall ing pathw ays[J] J Cell Sci,2003,116(16):3277-3284. 被引量:1
  • 10Bing Shu, Ming Zhang, Rong Xie,et al. BMP2, but not BMP4,is crucial for chondrocyte proliferation and maturation during endochondral bone development[J].J Cell Sci,2011,124(20):3428-3440. 被引量:1

二级参考文献150

共引文献79

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