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血管内皮祖细胞对组织工程骨成骨能力影响的实验研究 被引量:6

An experimental study on effects of bone forming ability of endothelial progenitor cells with tissue engineering bone in repairing segmental defects of rabbit radius
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摘要 目的观察血管内皮祖细胞(EPCs)对组织工程骨修复兔桡骨大段骨缺损时成骨能力的影响。方法自体骨髓通过不同方法的体外培养,获得EPCs及经成骨诱导的MSCs,与DBM构建组织工程骨修复兔桡骨大段骨缺损,观察术后不同时期的影像学及骨密度改变。结果术后2周,EPCs组与对照组的X线观察及骨密度差异无统计学意义。术后4、8、12周,EPCs组的骨密度明显高于对照组,X线示EPCs组骨痂明显多于对照组,8周可见EPCs组髓腔部分再通,对照组髓腔尚封闭。12周EPCs组新生骨密度均匀,髓腔已完全再通,对照组新生骨仍可见部分低密度区,髓腔大部分再通。术后16周,两组骨密度差异无统计学意义,X线示EPCs组新生骨已基本完成塑形,对照组髓腔完全再通,新生骨处于重建塑形期。结论EPCs可以促进组织工程骨修复大段骨缺损时的成骨能力,加速骨愈合。 Objective To investigate the effects of endothelial progenitor cells (EPCs) on the bone forming ability of tissue engineering bone during rabbit radius segmental defect healing. Methods The bone marrow mesenchymal stem cells (MSCs) and EPCs of the same rabbits were harvested from bone marrow and cultured in different conditions in vitro. They were seeded on decalcified bone matrix (DBM) to be tissue engineering bone, then implanted into the radius long segmental bone defects of the donor rabbit. The changes of X-ray and bone mineral density (BMD) at the defect site were analyzed at postoperation and the 2nd, 4th, 8th and 16th week after operation to evaluate the healing of the bone defects. Results There were no difference of X-ray and BMD at 2nd week after operation between EPCs group and control group. But at the 4th, 8th and 12th week, the BMD was significantly higher in EPCs group than that in control group. X-ray showed that the callus was much more in EPCs group. From the 8th week, the bone marrow cavity could be seen in EPCs group but not in MSCs group. At the 12th week, the BMD of new bone was well proportioned and the bone marrow cavity re-opened completely in EPCs group. While in control group, some low density area could be seen in X-ray and most of the bone marrow cavity re-opened. At the 16th week, BMD had no significant difference between EPCs group and control group, X-ray showed the new bone had finished reconstruction in EPCs group. While the bone marrow cavity reopened completely and new bones were reconstructing in control group. Conclusion EPCs can improve bone forming ability of tissue engineering bone in repairing segmental bone defect.
出处 《重庆医学》 CAS CSCD 2006年第22期2058-2059,2062,共3页 Chongqing medicine
关键词 血管内皮祖细胞 组织工程 骨缺损 X线 骨密度 endothelial progenitor cells tissue engineering bone defect X-ray bone mineral density
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参考文献8

  • 1许建中.骨组织工程的研究与开发进展[J].第三军医大学学报,2005,27(16):1625-1627. 被引量:10
  • 2Griffith LG,Naughton G.Tissue engineering-current challenges and expanding opportunities[J].Science,2002,295(5557):1009 被引量:1
  • 3杨志明,樊征夫,解慧琪,秦廷武,彭文珍.组织工程化人工骨血管化研究[J].中华显微外科杂志,2002,25(2):119-122. 被引量:49
  • 4Stahl A,Wu X,Wenger A,et al.Endothelial progenitor cell sprouting in spheroid cultures is resistant to inhibition by osteoblasts:a model for bone replacement grafts[J].FEBS Lett,2005,579(24):5338 被引量:1
  • 5Asahara T,Murohara T,Sullivan A.et al.Isolation of putative progenitor endothelial cells for angiogenesis[J].Science,1997,275(5302):964 被引量:1
  • 6Hristov M,Erl W,Weber PC.Endothelial progenitor cells:mobilization,differentiation and homing[J].Arterioscler Thromb Vasc Biol,2003,23(7):1185 被引量:1
  • 7Rehman J,Li J,Orschell CM,et al.Peripheral blood "endothelial progenitor cells"are derived from monocyte/macrophages and secrete angiogenic growth factors[J].Circulation,2003,107(8):1164 被引量:1
  • 8Asahara T,Masuda H,Takahashi T,et al.Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization[J].Circ Res,1999,85(3):221 被引量:1

二级参考文献22

  • 1秦辉,许建中,周强,王序全,罗飞,赵敏,朱灏.两种构建方法对组织工程骨种子细胞粘附和增殖的影响[J].第三军医大学学报,2004,26(11):990-992. 被引量:11
  • 2傅荣,杨志明.骨膜成骨细胞培养与生物活性陶瓷复合的实验研究[J].中国修复重建外科杂志,1996,10(4):197-201. 被引量:22
  • 3Niemeyer P, Seckinger A, Simank H G, et al.Allogenic transplantation of human mesenchymal stem cells for tissue engineering purposes:an in vitro study[ J]. Orthopade, 2004, 33 (12): 1346 - 1353. 被引量:1
  • 4Djouad F, Plence P, Bony C, et al. Immunosuppressive effect of mesenchymal stem cells favors tumor growth in allogeneic animals [J].Blood, 2003, 102(10): 3837 -3844. 被引量:1
  • 5Lazarus H M, Koc 0 N, Devine S M, et al. Cotransplantation of HLAidentical sibling culture-expanded mesenchymal stem cells and hematopoietic stem cells in hematologic malignancy patients [ J ]. Biol Blood Marrow Transplant, 2005, 11 (5): 389 -398. 被引量:1
  • 6Bartholomew A, Sturgeon C, Siatskas M, et al. Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo[J]. Exp Hematol, 2002, 30(1): 42 -48. 被引量:1
  • 7Deng W, Han Q, Liao L, et al. Long-term distribution of adult stem cells in different tissues after transplantation[ J]. Stem Cell and Cellular Therapy, 2003, 1 ( 1 ): 62 - 65. 被引量:1
  • 8Devine S M, Cobbs C, Jennings M, et al. Mesenchymal stem cells distribute to a wide range of tissues following systemic infusion into nonhuman primates[ J]. Blood, 2003, 101 (8): 2999 - 3001. 被引量:1
  • 9Aggarwal S, Pittenger M F. Human mesenchymal stem cells modulate allogeneic immune cell responses[ J]. Blood, 2005, 105 (4): 1815-1822. 被引量:1
  • 10Le Blanc K, Rasmusson I, Gotherstrom C, et al. Mesenchymal stem cells inhibit the expression of CD25 (interleukin-2 receptor ) and CD38 on phytohaemagglutinin-activated lymphocytes[ J]. Scand J Immunol, 2004, 60(3): 307 -315. 被引量:1

共引文献57

同被引文献97

  • 1曾宪利,裴国献,金丹,唐光辉,王学明,刘晓霞,曾俊岭,张文高.血管化组织工程骨修复猕猴胫骨缺损模型的建立及初步观察[J].中华创伤骨科杂志,2005,7(4):353-357. 被引量:30
  • 2王永刚,裴国献.血管束植入在组织工程骨血管化构建中的作用[J].解放军医学杂志,2007,32(1):26-28. 被引量:17
  • 3Jun-ho JANG,Sun-kyung KIM,Jeong-eun CHOI,Young-jin KIM,Hyun-woo LEE,Seok-yun KANG,Joon-seong PARK,Jin-hyuk CHOI,Ho-yeong LIM,Hugh C KIM.Endothelial progenitor cell differentiation using cryopreserved,umbilical cord blood-derived mononuclear cells[J].Acta Pharmacologica Sinica,2007,28(3):367-374. 被引量:11
  • 4Asahara T, Murohara T, Sullivan A, et al. Isolation of putative progenitor endothelial cells for angiogenesis[J]. Science, 1997, 275 (5302): 964-967. 被引量:1
  • 5Reyes M, Dudek A, Jahagirdar R, et al. Origin of endothelial progenitors in human postnatal bone marrow [J]. Clin Invest, 2002, 109 (3): 337-346. 被引量:1
  • 6Martinez-Estrada O M,Munoa S Y, Julve J, et al. Human adipose tissue as a source of Flk-1^+ cells: new method of differentiaion and expansion[J]. Cardiovasc Res, 2005, 6(2): 328-333. 被引量:1
  • 7Kaushal S, Amiel G E, Guleserian K J, et al. Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo[J]. Nat Med, 2001, 7(9): 1035-1040. 被引量:1
  • 8Asahara T, Takahashi T, Masuda H, et al. VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells[J]. EMBOJ, 1999, 18 (14): 3964- 3972. 被引量:1
  • 9Peiehev M, Naiyer A T, Pereira D, et al.Expression of VEGFR -2 and AC133 by circulating human CD34^+ cells identifies a population of functional endothelial precursors[J]. Blood, 2000, 95(3): 952-958. 被引量:1
  • 10Harraz M, Jiao C, Hanlon H D, et al. CD34-blood-derived human endothelial cell progenitors[J]. Stem Cells, 2001, 19 (4): 304-312. 被引量:1

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