›› 2013, Vol. 33 ›› Issue (6): 371-375.

• 基础与临床研究 • 上一篇    下一篇

大鼠骨髓基质细胞促进自体骨形成的实验研究

王芳,杨关鑫,赵玉红   

  1. 杭州市余杭区第五人民医院
  • 收稿日期:2013-02-06 修回日期:2013-03-14 出版日期:2013-06-28 发布日期:2013-07-12
  • 通讯作者: 王芳 E-mail:dentistonline@163.com
  • 基金资助:
    2009年度余杭区科技发展计划项目

Experimental research on rat bone marrow stromal cells promoting self bone formation

  • Received:2013-02-06 Revised:2013-03-14 Online:2013-06-28 Published:2013-07-12
  • Contact: Fang Wang E-mail:dentistonline@163.com

摘要: 目的 研究自体骨髓基质细胞 (bone marrow stromal cells, BMSCs)体外诱导扩增与仿生纳米壳聚糖-胶原复合支架材料(nano chitosan sodium collagen scaffold,NCSCS)复合修复骨缺损的可行性。方法 分离纯化wistar大鼠BMSCs,诱导BMSCs向成骨细胞(osteoblast,OB)转化,经碱性磷酸酶、茜素红组织化学染色鉴定,将BMSCs复合仿生纳米壳聚糖-胶原复合支架材料(nano chitosan sodium collagen scaffold,NCSCS)扫描电镜观察。制作wistar大鼠胫骨骨缺损模型,缺损处NCSCS-BMSCs复合物移植后观察骨缺损修复成骨情况。结果 扫描电镜下BMSCs细胞在仿生纳米壳聚糖-胶原复合支架材料上大面积生长。BMSCs复合仿生纳米壳聚糖-胶原复合支架材料植入2周后,材料周围可见大量纤维组织,并可见成骨细胞和少量新生的骨样基质,新生骨对照组和实验组比较差别显著(P<0.01);植入6周后,可见到材料与新生骨之间相互混杂,中有纤维相间隔,和原有骨界面尚清晰可辨认,材料部分降解,对照组和实验组比较新生骨有统计学差别(P<0.05);植入12周后,材料几乎降解完全,和天然骨组织界面可见新骨形成,对照组和实验组比较新骨形成无统计学差别(P>0.05)。材料降解在各时间段对照组和实验组比较差别不显著(P>0.05)。结论 BMSCs介导NCSCS修复骨缺损优于单纯的NCSCS修复骨缺损,尤以早期效果为好。

关键词: BMSCs, NCSCS, bone defects, rat

Abstract: Objective To study the feasibility of bone defect repair with in vitro induced BMSCs combined with NCSCS material. Methods Isolate and purify wistar rat BMSCs, and induce BMSCs to osteoblasts, which were identified by alkaline phosphataseand and alizarin red histochemical staining. BMSCs on the NCSCS were observed by scanning electron microscope. Wistar rat tibia bone defect model was built. Implant NCSCS-BMSCs complex material to bone defects, and observe the bone formation. Results Large scale of BMSCs proliferated on the NCSCS material under scanning electron microscope. Two weeks after the NCSCS-BMSCs were implantated, a great amount of fiber tissues with osteoblasts and some osteoid matrix were found around the material. There were statistical difference in the percentage of newbone between the experimental and the control groups(P<0.01). 6 weeks after NCSCS-BMSCs were implantated, newbone infiltrated into NCSCS, with fiber between them, and the original bone interface was still clear and could still be identified. Part of the NCSCS were degradated, and there were statistical difference in the percentage of newbone between the experimental and the control groups(P<0.05). 12 weeks after the NCSCS-BMSCs were implantated, NCSCS were almost entirely degradated, and newbone were found on the original bone interface. There was no difference in new bone formation between these two groups(P>0.05). The degradation of the NCSCS showed no significant difference between the experimental and the control groups at different time points. Conclusion NCSCS-BMSCs are better than NCSCS alone in repair of bone defects, especially in the early-term effect.

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