Jiang Fang, Xiao Ji-Jie, Lu Yuan-Ting, Li Wei, Duan Yu-Wen, Sheng Zong-Hai, Li Shao-Lin
Department of Imaging, Third Affiliated Hospital of Southern Medical University, Guangzhou 510630, China.E-mail:
Nan Fang Yi Ke Da Xue Xue Bao. 2017 May 20;37(5):652-658. doi: 10.3969/j.issn.1673-4254.2017.05.14.
To observe the effect of superparamagnetic iron oxide (SPIO) on the differentiation of rat bone marrow stem cells (BMSCs) into chondrocytes in vitro and explore the possible mechanism.
CCK8 assay was performed to examine the cytotoxicity of SPIO (1 and 5 µg/mL) on cultured SD rat BMSCs. Prussian blue staining and fluorescence excitation assay were used to assess the binding of the SPIO to BMSCs after the cells had been cultured in chondrocytes-induced medium in the presence of SPIO (1 and 5 µg/mL) for 9 days. The mRNA levels of COL2 α2, aggrecan and MMP13 in the cell culture were examined using Q-PCR, and the chondrogenic differentiation of the BMSCs was analyzed using alcian blue staining and immunofluorescence staining for COL2 α2. The protein levels of COL2 α2, aggrecan, MMP13, Ihh and PTHrP in the cells were examined using Western blotting.
CCK8 assay showed no significant toxicity of SPIO on BMSCs. Compared with the control cells, the cells cultured in the presence of SPIO showed increased expressions of COL2 α2 and aggrecan and decreased expression of MMP13 at both mRNA and protein levels with also significantly increased expressions of Ihh and PTHrP proteins.
SPIO can promote the differentiation of rat BMSCs into chondrocytes and up-regulate the Ihh/PTHrP signal pathway, suggesting the potential of SPIO as a new therapeutic agent for chondrocyte-related diseases.
观察超顺磁性氧化铁(SPIO)对大鼠骨髓干细胞(BMSCs)体外向软骨细胞分化的影响,并探讨其可能机制。
采用CCK8法检测SPIO(1和5μg/mL)对培养的SD大鼠BMSCs的细胞毒性。在含有SPIO(1和5μg/mL)的软骨细胞诱导培养基中培养细胞9天后,用普鲁士蓝染色和荧光激发试验评估SPIO与BMSCs的结合情况。采用Q-PCR检测细胞培养物中COL2α2、聚集蛋白聚糖和MMP13的mRNA水平,并用阿尔新蓝染色和COL2α2免疫荧光染色分析BMSCs的软骨分化情况。采用蛋白质印迹法检测细胞中COL2α2、聚集蛋白聚糖、MMP13、Ihh和PTHrP的蛋白水平。
CCK8试验显示SPIO对BMSCs无明显毒性。与对照细胞相比,在SPIO存在下培养的细胞在mRNA和蛋白水平上COL2α2和聚集蛋白聚糖的表达增加,MMP13的表达降低,Ihh和PTHrP蛋白的表达也显著增加。
SPIO可促进大鼠BMSCs向软骨细胞分化并上调Ihh/PTHrP信号通路,提示SPIO作为软骨细胞相关疾病新型治疗药物的潜力。