期刊文献+

骨形态发生蛋白-2基因修饰的组织工程化骨修复羊胫骨干骨缺损 被引量:25

BMP-2 gene modified tissue-engineered bone repairing segmental tibial bone defects in goats
原文传递
导出
摘要 目的 评价腺病毒介导的人骨形态发生蛋白 2 (Adv hBMP 2 )基因转染的组织工程化人工骨对大动物长骨干骨缺损的修复效果。方法 建立羊胫骨干骨缺损模型 (2 .6cm) ,单侧 (右 )植入体外构建的组织工程化骨 ,2 6只羊分为 5组 :(1)Adv hBMP 2转染的骨髓间充质干细胞 (BMSC)加煅烧骨 (CB)组 (9侧 ) ;(2 )腺病毒介导的 β 半乳糖苷酶 (Adv βgal)基因转染的BMSC加CB组 (6侧 ) ;(3)未转染的BMSC加CB组 (6侧 ) ;(4)单纯CB组 (3侧 ) ;(5 )未治疗组 (2侧 )。分期行X线、计量组织学检查和生物力学测定。结果 X线 :4~ 8周 ,Adv hBMP 2转染组的羊胫骨干骨缺损内有明显骨痂形成 ;2 6周 ,(1)、(2 )、(3)、(4)和 (5 )组的完全愈合率 ,分别为 5 / 8、1/ 5、0 / 5、0 / 2、0 / 1。计量组织学示 ,与其他组相比 ,1组的新生骨量最多 ,并有皮质骨形成 ;第 1组移植骨的压缩载荷和弹性模量明显大于其他各组。结论 hBMP 2基因修饰的组织工程化人工骨可以修复大动物 (羊 )负重骨 (胫骨 )的节段性缺损。 Objective To evaluate the effectiveness of the tissue-engineered bone substitute loaded with adenovirus mediated human bone morphogenetic protein-2 gene (Adv-hBMP-2)transfected bone marrow derived mesenchymal stem cells(BMSC)in the repair of diaphyseal segmental bone defect of large animal. Methods The right tibial bone defects (2.6 cm) model of 26 goats were established and divided into 5 groups: I.Adv-hBMP-2 transfected BMSC/calcined bone(CB) group ( n =9); II.adenovirus-β-galactosidase (Adv-βgal) gene transfected BMSC/CB group ( n =6); III.untransfected BMSC/CB group ( n =6); IV.single CB group ( n =3); VI.untreated group ( n =2). The above tissue-engineered bone substitutes were implanted in the bone defects respectively except group VI. Roentgenography, histomorphometrical analysis and biomechanical measurement were studied at various times. Results X-ray: at 4~8 th weeks after implantation, more bony callus was found in the bone defects of group I. The complete healing rates of group I, II, III, IV, and V were 5/8, 1/5, 0/5, 0/2, 0/1 respectively at 26 th week after implantation. Histomorphometrical analysis showed much more new bony callus including cortical bone formed in group I than those of other groups. The compression strength of the implanted bone substitute of group I is significantly higher than those of group II and III. Conclusion The tissue-engineered bone substitute loaded with human BMP-2 gene transfected BMSC can repair diaphyseal segmental bone defect of large animal (goat).
出处 《中华医学杂志》 CAS CSCD 北大核心 2003年第15期1345-1349,共5页 National Medical Journal of China
基金 上海市重点科技发展项目 (0 1JC14 0 2 8) 上海市科委国际合作项目 (0 14 3 0 70 2 1)
关键词 骨形态发生蛋白-2 基因修饰 组织工程化骨 修复 胫骨干骨缺损 骨代用品 骨再生 Bone morphogenetic proteins Gene therapy Stem cells Bone regenerations Bone substitutes Human engineering
  • 相关文献

参考文献12

  • 1Lou J, Xu F, Merkel K, et al. Gene therapy: adenovirus-mediated human bone morphogenetic protein-2 gene transfer induces mesenchymal progenitor cell differentiation in vitro,bone formation in vivo. J Orthop Res,1999,17:43-50.
  • 2朱六龙,戴克戎,汤亭亭,郁朝锋,徐旻,徐小良,楼觉人.骨形成蛋白-2基因转染人骨髓间质干细胞诱导异位成骨的实验研究[J].中国修复重建外科杂志,2003,17(2):131-135. 被引量:21
  • 3Lieberman JR, Daluiski A, Stevenson S, et al. The effect of regional gene therapy with bone morphogenetic protein-2-producing bone-marrow cells on the repair of segmental femoral defects in rats. J Bone and Joint Surg,1999,81-A:905-917.
  • 4Tsuchida H, Hashimoto J, Lou J, et al. Engineered allogeneic mesenchymal stem cells repair femoral segmental defect in rats. J Orthop Res,2003,21:44-53.
  • 5徐小良,戴克戎,汤亭亭,郁朝锋,徐旻,朱六龙,朱振安,楼觉人.腺病毒介导的人骨形态发生蛋白2基因修复兔桡骨缺损[J].中华创伤杂志,2002,18(11):677-680. 被引量:24
  • 6Riew KD, Wright NM, Lou J, et al. Induction of bone formation using a recombinant adenoviral vecter carrying the human BMP-2 gene in a rabbit spinal fusion model. Calcified Tissue International, 1998,63:357-360.
  • 7Reddi AH. Bone morphogenetic proteins: from basic science to clinical applications J Bone and Joint Surg, 2001, 83A (S1): 1-6.
  • 8John MW, Vicki R. Bone morphogenetic protein and bone morphogenetic protein gene family in bone formation and repair. Clin Orthop,1998,346:26-37.
  • 9Baltzer AWA, Lattermann C, Whalen JD, et al. Potential role of direct adenoviral gene transfer in enhancing fracture repair. Clin Orthop,2000,379:S120-S125.
  • 10Blokhuis TJ, Wippermann BW, Haarman HJ,et al. Resorbable calcium phosphate particles as a carrier material for bone marrow in an ovine segmental defect. J Biomed Mater Res,2000,51:369-375.

二级参考文献15

  • 1Bruder SP;Kraus KH;Goldberg VM.The effect of implants loaded with autologous mesenchymal stem cells on the healing of canine segmental bone defects,1998(07).
  • 2Bruder SP;Jaiswal N;Ricalton NS.Mesenchymal stem cells in osteobiology and appiled bone regeneration,1998.
  • 3Rogers J J;Young HE;Adkison LR.Differentiation factors induce expression of muscle,fat,cartilage,and bone in a clone of mouse pluripotent mesenchymal stem cells,1995.
  • 4Wakitani S;Saito T;Caplan AI.Myogenic cells derived from rat bone marrow mesenchymal stem cells exposed to 5-azacytidine[J],1995(12).
  • 5Cheng SL;Lou J;Wright NM.In vitro and in vivo induction of bone formation using a recombinant adenoviral vector carrying the human BMP-2 gene[J],2001(02).
  • 6Caplan AI.Mesenchymal stem cells[J],1991(05).
  • 7Haynesworth SE;Goshima J;Goldberg VM.Characterizatiom of cells with osteogenic potential from human marrow[J],1992(01).
  • 8Young RG;Butler DL;Weber W.Use of mesenchymal stem cells in a collagen matrix for achilles tendon repair[J],1998(04).
  • 9Lou J;Xu F;Merkel K.Gene therapy: adenovirus-mediated human bone morphogenetic protein-2 gene transfer induces mesenchymal progenitor cell proliferation differentiation in vitro and bone formation in vivo[J],1999(01).
  • 10Lieberman JR;Daluiski A;Steverson S.The effect of regional gene therapy with bone morphogenetic protein-2-produ-cing bone-marrow cells on the repair of segmental femoral defect in rats,1999(07).

共引文献43

同被引文献304

引证文献25

二级引证文献124

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