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骨形态发生蛋白7/聚(丙交酯-共-乙交酯)微球对兔骨髓间充质干细胞增殖及成软骨分化的影响

[Effect of bone morphogenetic protein 7/poly (lactide-co-glycolide) microspheres on the proliferation and chondrogenic differentiation of rabbit bone marrow mesenchymal stem cells].

作者信息

Chen Jialei, Liu Ming, Duan Xin, Huang Fuguo, Xiang Zhou

机构信息

Department of Orthopeadics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R.China.

Department of Orthopeadics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041,

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2018 Apr 15;32(4):428-433. doi: 10.7507/1002-1892.201711093.

Abstract

OBJECTIVE

To evaluate the effect of bone morphogenetic protein 7 (BMP-7)/poly (lactide-co-glycolide) (PLGA) microspheres on proliferation and chondrogenic differentiation of rabbit bone marrow mesenchymal stem cells (BMSCs).

METHODS

BMP-7/PLGA microspheres were fabricated by double emulsion-drying in liquid method. After mixing BMP-7/PLGA microspheres with the chondrogenic differentiation medium, the supernatant was collected on the 1st, 3rd, 7th, 14th, and 21st day as the releasing solution. The BMSCs were isolated from the bilateral femurs and tibias of 3-5 days old New Zealand rabbits, and the 3rd generation BMSCs were divided into 2 groups: microspheres group and control group. The BMSCs in microspheres group were cultured by 200 μL BMP-7/PLGA microspheres releasing solution in the process of changing liquid every 2-3 days, while in control group were cultured by chondrogenic medium. The cell proliferation (by MTT assay) and the glycosaminoglycan (GAG) contents (by Alician blue staining) were detected after chondrogenic cultured for 1, 3, 7, 14, and 21 days. The chondrogenic differentiation of BMSCs was observed by safranine O staining, toluidine blue staining, and collagen type Ⅱ immunohistochemistry staining at 21 days.

RESULTS

MTT test showed that BMSCs proliferated rapidly in 2 groups at 1, 3, and 7 days; after 7 days, the proliferation of BMSCs in the control group was slow and the BMSCs in microspheres group continued to proliferate rapidly. There was no significant difference of the absorbance ( ) value at 1, 3, and 7 days between 2 groups ( >0.05), but the value at 14 and 21 days in microspheres group was significantly higher than that in control group ( <0.05). Compared with control group at 21 days, in microsphere group, almost all nuclei were dyed bright red by safranine O staining, almost all the nuclei appeared metachromatic purple red by toluidine blue staining, and the most nuclei were yellow or brown by immunohistochemical staining of collagen type Ⅱ. Alcian blue staining showed that the content of GAG in 2 groups increased continuously at different time points; after 7 days, the increasing trend of the control group was slow and the microspheres group continued hypersecretion. There was no significant difference of the GAG content at 1, 3, and 7 days between 2 groups ( >0.05), but the GAG content at 14 and 21 days in microspheres group was significantly higher than that in control group ( <0.05).

CONCLUSION

BMP-7/PLGA microspheres prepared by double emulsion-drying in liquid method can promote proliferation and chondrogenic differentiation of rabbit BMSCs.

摘要

目的

评估骨形态发生蛋白7(BMP - 7)/聚乳酸 - 乙醇酸共聚物(PLGA)微球对兔骨髓间充质干细胞(BMSCs)增殖和软骨分化的影响。

方法

采用液中双乳化干燥法制备BMP - 7/PLGA微球。将BMP - 7/PLGA微球与软骨分化培养基混合后,分别在第1、3、7、14和21天收集上清液作为释放液。从3 - 5日龄新西兰兔双侧股骨和胫骨中分离BMSCs,将第3代BMSCs分为2组:微球组和对照组。微球组BMSCs在每2 - 3天换液过程中用200 μL BMP - 7/PLGA微球释放液培养,而对照组用软骨分化培养基培养。软骨诱导培养1、3、7、14和21天后,检测细胞增殖(MTT法)和糖胺聚糖(GAG)含量(阿利新蓝染色法)。在21天时,通过番红O染色、甲苯胺蓝染色和Ⅱ型胶原免疫组织化学染色观察BMSCs的软骨分化情况。

结果

MTT试验显示,两组BMSCs在第1、3和7天时均快速增殖;7天后,对照组BMSCs增殖缓慢,微球组BMSCs继续快速增殖。两组在第1、3和7天时吸光度( )值无显著差异( >0.05),但微球组在第14和21天时的 值显著高于对照组( <0.05)。与21天时的对照组相比,微球组中,番红O染色几乎所有细胞核染成鲜红色,甲苯胺蓝染色几乎所有细胞核呈现异染紫红色,Ⅱ型胶原免疫组织化学染色多数细胞核为黄色或棕色。阿利新蓝染色显示,两组在不同时间点GAG含量均持续增加;7天后,对照组增加趋势缓慢,微球组持续高分泌。两组在第1、3和7天时GAG含量无显著差异( >0.05),但微球组在第14和21天时的GAG含量显著高于对照组( <0.05)。

结论

采用液中双乳化干燥法制备的BMP - 7/PLGA微球可促进兔BMSCs的增殖和软骨分化。

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