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BMSCs复合胶原材料三维诱导软骨细胞的初步研究
引用本文:胡炜,项舟,张学利,周海涛,杨志明.BMSCs复合胶原材料三维诱导软骨细胞的初步研究[J].中国修复重建外科杂志,2008,22(2):153-156.
作者姓名:胡炜  项舟  张学利  周海涛  杨志明
作者单位:1. 天津市人民医院脊柱外科
2. 四川大学华西医院骨科,成都,610041
3. 四川大学华西医院生物治疗国家重点实验室·干细胞与组织工程研究室
摘    要:目的 通过体外培养犬BMSCs,以胶原海绵作为支架材料,体外三维复合培养后,观察向软骨细胞定向诱导的可行性. 方法 健康家犬10只,体重10~15 kg,雌雄不拘.抽取骨髓,体外培养BMSCs,传至第3代,倒置相差显微镜观察细胞形态.实验组将第3代BMSCs以1×106/mL密度接种于胶原海绵支架材料,体外培养48 h后,将细胞材料复合物以软骨细胞定向诱导培养基进行诱导,每隔2天换液;对照组将第3代BMSCs以相同密度接种于胶原海绵支架材料,每隔2天以DMEM换液.培养后14 d,将细胞材料复合物行HE染色和免疫组织化学染色观察. 结果 倒置相差显微镜下第3代BMSCs与第2代BMSCs形态基本一致,传代初期细胞伸出伪足,呈梭形或三角形,7 d后逐渐以梭形为主,胞体饱满,细胞传代后增长速度明显加快.组织学观察实验组细胞广泛分布于支架材料孔隙内,多数细胞呈多角形或者不规则形,少数呈短梭形,细胞周围间隙可见基质成分;对照组细胞分布于支架材料孔隙内,呈梭形或圆形,核呈圆形或椭圆形,胞体较大,胞质透亮均匀,细胞核轮廓清楚,呈蓝色.免疫组织化学染色显示,实验组支架材料孔隙内的细胞胞浆可见棕黄色颗粒,细胞周围出现黄染区;对照组无表达. 结论 BMSCs接种于胶原海绵材料后,经定向软骨诱导后,可向软骨组织方向分化.

关 键 词:组织工程软骨  BMSCs  Ⅰ型胶原  软骨细胞    胶原材料  三维  软骨细胞  研究  COLLAGEN  STUDY  CARTILAGE  INDUCED  MATRICES  方向  软骨组织  软骨诱导  定向  海绵材料  表达  黄染  颗粒  细胞胞浆  染色显示  免疫组织化学
收稿时间:2007-08-06
修稿时间:2007-09-17

PRELIMINARY STUDY OF BMSCs SEEDED INTO COLLAGEN Ⅰ-GLYCOSAMINOGLYCAN MATRICES INDUCED TOWARD CARTILAGE
HU Wei,XIANG Zhou,ZHANG Xueli,ZHOU Haitao,YANG Zhiming.PRELIMINARY STUDY OF BMSCs SEEDED INTO COLLAGEN Ⅰ-GLYCOSAMINOGLYCAN MATRICES INDUCED TOWARD CARTILAGE[J].Chinese Journal of Reparative and Reconstructive Surgery,2008,22(2):153-156.
Authors:HU Wei  XIANG Zhou  ZHANG Xueli  ZHOU Haitao  YANG Zhiming
Institution:Department of Orthopaedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R. China.
Abstract:OBJECTIVE: To investigate the possibility of BMSCs seeded into collagen I -glycosaminoglycan (CG) matrices to form the tissue engineered cartilage through chondrocyte inducing culture. METHODS: Bone marrow aspirate of dogs was cultured and expanded to the 3rd passage. BMSCs were harvested and seeded into the dehydrothemal treatment (DHT) cross-linked CG matrices at 1 x 10(6) cells per 9 mm diameter sample. The samples were divided into experimental group and control group. In the experimental group, chondrogenic differentiation was achieved by the induction media for 2 weeks. Medium was changed every other day in both experimental group and control group. The formation of cartilage was assessed by HE staining and collagen II immunohistochemical staining. RESULTS: The examinations under the inverted phase contrast microscope indicated the 2nd and 3rd passage BMSCs had the similar morphology. HE staining showed the BMSCs in the experimental group appeared polygon or irregular morphology in the CG matrices, while BMSCs in the control group appeared fibroblast-like spindle or round morphology in the CG matrices. Extracellular matrix could be found around cells in the experimental group. Two weeks after seeded, the cells grew in the CG matrices, and positive collagen II staining appeared around the cells in the experimental group. There was no positive collagen II staining appeared in the control group. CONCLUSION: It is demonstrated that BMSCs seeded CG matrices can be induced toward cartilage by induction media.
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