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[等轴拉伸应变在间充质干细胞早期分化为软骨细胞中的作用]

[Effect of equiaxial tensile strain in early differentiation of mesenchymal stem cells into cartilage cells].

作者信息

Yang Zi-Quan, Men Ya-Xun

机构信息

Department of Orthopaedic Surgery, the Second Affiliated Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi, China.

出版信息

Zhongguo Gu Shang. 2018 Sep 25;31(9):846-852. doi: 10.3969/j.issn.1003-0034.2018.09.013.

DOI:10.3969/j.issn.1003-0034.2018.09.013
PMID:30332879
Abstract

OBJECTIVE

To observe the effect of cyclic equiaxial tensile strain in the early differentiation of bone marrow mesenchymal stem cells(BMSCs) into cartilage in mouse under conditions of two-dimensional culture, and to investigate the mechanism of cyclic equiaxial tensile strain in early chondrogenic differentiation.

METHODS

Sixteen KM mouse aged 4 weeks were selected, male and female unlimited, with an average weight of 19.5 g (17 to 21 g). After extracting and isolating the BMSCs from KM mouse, then subculture the BMSCs to the 3rd generation. Seed the cells in the biological plate(BioFlex). According to experimental design, the cells were divided into 6 groups, blank group: ordinary culture medium was cultured for 8 days without isometric cyclic tensile strain stimulation. Control group: chondrogenic differentiation medium was used to culture for 8 days without isometric cyclic tensile strain stimulation. Experimental group: the experimental group was divided into 4 groups, all of which were cultured with chondrogenic differentiation medium for 8 days. During which isometric cyclic tensile strain stimulation was given for 1, 3, 5 and 7 days respectively. At the 8th day, all the cells were collected, the expression of the Sox9, Col-II and ROCK 1 signaling pathway-related molecules was analyzed by RT-PCR. Cells in each group were extracted, and the efficiency of cell proliferation in each group was detected by CCK-8. Glycosaminoglycan content in medium changed last was detected using ELISA. Pericellular matrix was observed by Safranin O staining and Alcian Blue staining. Normal measurement data using mean±standard deviation compared between the blank group and control group using paired t-test, compared between the experimental group and relative group using single factor analysis of variance.

RESULTS

(1)After 8 days of culture, compared with the control group, the relative expression of Sox 9 and Col-II mRNA in the experimental group increased gradually with the increase of loading time(<0.05), while the relative expression of ROCK1 mRNA decreased(<0.05). Compared with the blank group, the relative expression of ROCK1 mRNA in experimental group and control group increased (<0.05). (2)With the increase of loading time, the experimental group showed a trend of decreasing at first and then increasing, but compared with the blank group and the control group, the control group decreased significantly. (3)Glycosaminoglycan content in the medium changed last was detected by ELISA. The glycosaminoglycans in the experimental group increased gradually, and the content changes on 7 days loading group were statistically significant compared with other groups(<0.05). (4)Safranin O and Alcilan staining showed that there was a tendency of cartilage differentiation in the experimental group, and the shape gradually increased with time, which was more obvious than that in the control group; The PCM, Col-II and GAG in the experimental group increased gradually with the increase of mechanical stimulation days, which were more obvious than those in the control group.

CONCLUSIONS

Under conditions of two-dimensional culture, in the early differentiation of mesenchymal stem cells into cartilage, cyclic equiaxial tensile strain can promote the proliferation of BMSCs and the differentiation into chondrocytes. Moreover, cyclic equiaxial tensile strain may promote chondrogenic differentiation through inhibiting the Rho/ROCK 1 signaling pathway.

摘要

目的

观察二维培养条件下周期性等轴拉伸应变对小鼠骨髓间充质干细胞(BMSCs)早期向软骨分化的影响,并探讨周期性等轴拉伸应变在早期软骨形成分化中的作用机制。

方法

选取4周龄KM小鼠16只,雌雄不限,平均体重19.5 g(17~21 g)。从KM小鼠中提取并分离BMSCs,然后传代培养至第3代。将细胞接种于生物板(BioFlex)。根据实验设计,将细胞分为6组,空白组:用普通培养基培养8天,无等轴循环拉伸应变刺激。对照组:用软骨分化培养基培养8天,无等轴循环拉伸应变刺激。实验组:实验组分为4组,均用软骨分化培养基培养8天。在此期间分别给予1、3、5和7天的等轴循环拉伸应变刺激。第8天,收集所有细胞,采用RT-PCR分析Sox9、Col-II和ROCK 1信号通路相关分子的表达。提取每组细胞,采用CCK-8检测每组细胞的增殖效率。采用ELISA检测培养基中最后变化的糖胺聚糖含量。采用番红O染色和阿尔辛蓝染色观察细胞周围基质。计量资料以均数±标准差表示,空白组与对照组比较采用配对t检验,实验组与相关组比较采用单因素方差分析。

结果

(1)培养8天后,与对照组相比,实验组中Sox 9和Col-II mRNA的相对表达量随加载时间的增加而逐渐升高(<0.05),而ROCK1 mRNA的相对表达量降低(<0.05)。与空白组相比,实验组和对照组ROCK1 mRNA的相对表达量升高(<0.05)。(2)随着加载时间的增加,实验组呈先下降后上升趋势,但与空白组和对照组相比,对照组下降明显。(3)采用ELISA检测培养基中最后变化的糖胺聚糖含量。实验组糖胺聚糖逐渐增加,加载7天组的含量变化与其他组相比差异有统计学意义(<0.05)。(4)番红O和阿尔辛蓝染色显示实验组有软骨分化倾向,且形态随时间逐渐增加,比对照组更明显;实验组的细胞周围基质、Col-II和GAG随机械刺激天数的增加而逐渐增加,比对照组更明显。

结论

在二维培养条件下,间充质干细胞早期向软骨分化过程中,周期性等轴拉伸应变可促进BMSCs的增殖并向软骨细胞分化。此外,周期性等轴拉伸应变可能通过抑制Rho/ROCK 1信号通路促进软骨形成分化。

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