| 骨髓间质干细胞体外定向诱导分化为软骨细胞的实验研究 |
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投稿时间：2007-08-16
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| 作者 | Author | 单位 | Address | E-Mail |
| 同志超 |
TONG Zhi-chao |
西安市红十字会医院骨科，陕西 西安 710054 |
Department of Orthopaedics,Xi'an Red Cross Society Hospital,Xi'an 710054,Shaanxi,China |
zhichaotong@126.com |
| 杨镇 |
YANG Zhen |
西安市红十字会医院骨科，陕西 西安 710054 |
Department of Orthopaedics,Xi'an Red Cross Society Hospital,Xi'an 710054,Shaanxi,China |
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| 同志勤 |
TONG Zhi-qin |
西安交通大学第二医院骨科 |
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| 王坤正 |
WANG Kun-zheng |
西安交通大学第二医院骨科 |
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| 杨团民 |
YANG Tuan-min |
西安市红十字会医院骨科，陕西 西安 710054 |
Department of Orthopaedics,Xi'an Red Cross Society Hospital,Xi'an 710054,Shaanxi,China |
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| 石宗利 |
SHI Zong-li |
兰州交通大学机电工程学院材料研究所 |
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| 李毅 |
LI Yi |
西安市红十字会医院骨科，陕西 西安 710054 |
Department of Orthopaedics,Xi'an Red Cross Society Hospital,Xi'an 710054,Shaanxi,China |
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| 郭雄 |
GUO Xiong |
西安交通大学骨病研究所 |
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| 期刊信息：《中国骨伤》2008年，第21卷，第5期，第362-364页 |
| DOI：doi:10.3969/j.issn.1003-0034.yyyy.nn.zzz |
| 基金项目:陕西省社会发展攻关项目(编号：2002K10-G1) |
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中文摘要:
目的：探讨分离骨髓间充质干细胞(MSCs)并诱导其向软骨细胞转化的体外培养方法，为软骨组织工程的种子细胞来源提供实验依据。
方法：抽取兔髂骨骨髓液，经梯度离心法和贴壁法进行体外培养，贴壁细胞传代，取第3代细胞在培养基中添加软骨分化诱导剂[转化生长因子(TGF-β2)10 ng/ml、地塞米松10-7 mol/L、维生素C 50 μmol/L],经7、14、21 d诱导培养后，倒置显微镜观察细胞形态，免疫组织化学染色检测软骨特异性Ⅱ型胶原表达。将诱导细胞与软骨支架材料--聚磷酸钙纤维/左旋聚乳酸(CPP/PLLA)复合，1周后终止培养，扫描电镜观察细胞黏附情况。
结果：诱导后细胞体外扩增能力显着降低，细胞形态由成纤维样梭形向多角形、多边形或类圆形转变，诱导21 d后细胞形态变化最为显着，Ⅱ型胶原免疫组化染色深而均匀。诱导后的MSCs可在支架材料内良好黏附生长。
结论：体外培养的MSCs可定向诱导分化为软骨细胞，分泌软骨细胞特异性基质，可用作软骨组织工程的种子细胞。 |
| 【关键词】骨髓 间充质干细胞 软骨细胞 组织工程 |
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| Study of inducing bone marrow-derived mesenchymal stem cells into chondrocytes in vitro |
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ABSTRACT
Objective: To explore a method of isolation,culture and chondrogenic phenotype differentiation of mesenchymal stem cells(MSCs) from the bone marrow of rats in vitro and to offer experimental reference for the resources of seeding cells in cartilage tissue engineering.
Methods: MSCs were isolated from bone marrow and purified by density gradient centrifuge and cultured in vitro. The MSC adherence formed and those in passage 3 were chosen to induce into chondrogenic differentiation. After 7,14,21 days,immunohistochemical techique was applied to detect the expression of collagen typeⅡ。 The differentiated cells were implanted on the CPP/PLLA composites. After the cell-scaffold complex was cultured in vitro for one week,the ultrastructure of the scaffold was observed with scanning electron microscopy.
Results: The differentiated cells changed from a spindle-like fibroblastic appearance to a polygonal shape,the capability of proliferation was down markedly. Immunohistochemical staining of collagen II were positive for the pass age,especially in the 21st days. Induced MSCs were well adherent to the scaffold composites and the cells were embedded by the cell-matrix.
Conclusion: Under the induced medium,MSCs can differentiate into chondrogenic phenotype and secrete specificity matrix of cartilage in vitro. MSCs can likely be served as optimal cell source for cartilage tissue engineering. |
| KEY WORDS Bone marrow Mesenchymal stem cells(MSCs) Chondrocytes Tissue engineering |
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| 引用本文，请按以下格式著录参考文献： |
| 中文格式: | 同志超,杨镇,同志勤,王坤正,杨团民,石宗利,李毅,郭雄.骨髓间质干细胞体外定向诱导分化为软骨细胞的实验研究[J].中国骨伤,2008,21(5):362~364 |
| 英文格式: | TONG Zhi-chao,YANG Zhen,TONG Zhi-qin,WANG Kun-zheng,YANG Tuan-min,SHI Zong-li,LI Yi,GUO Xiong.Study of inducing bone marrow-derived mesenchymal stem cells into chondrocytes in vitro[J].zhongguo gu shang / China J Orthop Trauma ,2008,21(5):362~364 |
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