Zhang H, Xu C, Liu Y, Yuan W
First Department of Spinal Surgery, Changzheng Hospital Affiliated to Second Military Medical University, Shanghai 200003, China.
Zhonghua Wai Ke Za Zhi. 2017 Mar 1;55(3):203-207. doi: 10.3760/cma.j.issn.0529-5815.2017.03.008.
To investigate the function and mechanism of miR-563 in regulating the ossification of posterior longitudinal ligament (OPLL) cells. Posterior longitudinal ligament cells were isolated and cultured from both OPLL patients (=6) and non-ossified ligament patients (PLL, =4) who underwent spine surgery from March to June 2015 in First Department of Spinal Surgery, Changzheng Hospital Affiliated to Second Military Medical University. The expression levels of miR-563 in OPLL and PLL groups were analyzed using real-time PCR. MicroRNA mimics were utilized to over express miR-563, and microRNA inhibitors were designed to knockdown its expression. Using the over expression and inhibition method, the level of Alizarin Red staining, alkaline phosphatase and ossification related genes in miR-563 were analyzed over expressed or inhibited and ossification induced ligament cells. After that the potential target of miR-563 was predicted using Targetscan and verified using dual-luciferase reporter assay. The results between the groups were compared by test. The expression level of miR-563 was significantly higher in OPLL than PLL groups (8.53±0.84 . 1.00±0.12, '=21.629, =0.000). The over expression of miR-563 resulted in higher level of alizarin red staining (2.52±0.25 .1.00±0.14), alkaline phosphatase activities (3.11±0.55 .1.00±0.11) and ossification related genes (RUNX2: 3.25±0.55 .1.00±0.10; IBSP: 2.35±0.32 . 1.00±0.14; 7.43 to 10.99, all =0.000), while the inhibition resulted in lower level (alizarin red staining: 0.52±0.21 . 1.00±0.12; alkaline phosphatase activities: 0.41±0.12 . 1.00±0.09; RUNX2: 0.35±0.13 . 1.00±0.12; IBSP: 0.55±0.12 .1.00±0.11; 4.36 to 8.45, all <0.05). Combining the prediction results of Targetscan and expression profiles between OPLL and PLL, SMURF1 was found as a potential target of miR-563, and dual-luciferase reporter assay also identified their relationship. By over expression, the expression level of SMURF1 was significantly decreased (0.25±0.06 .1.00±0.10, =-12.862, =0.000), which again verified the hypothesis. miRNA-563 significantly promotes the osteogenic differentiation of posterior longitudinal ligament cells and the mechanism of which is possibly through down regulating SMURF1.
探讨miR-563在调节后纵韧带骨化(OPLL)细胞中的作用及机制。从2015年3月至6月在第二军医大学附属长征医院脊柱外科一部接受脊柱手术的OPLL患者(n = 6)和非骨化韧带患者(PLL,n = 4)中分离并培养后纵韧带细胞。采用实时定量PCR分析OPLL组和PLL组中miR-563的表达水平。利用微小RNA模拟物使miR-563过表达,并设计微小RNA抑制剂来敲低其表达。采用过表达和抑制方法,分析miR-563过表达或抑制以及诱导骨化的韧带细胞中茜素红染色、碱性磷酸酶和骨化相关基因的水平。之后使用Targetscan预测miR-563的潜在靶标,并通过双荧光素酶报告基因检测进行验证。组间结果采用t检验进行比较。miR-563在OPLL组中的表达水平显著高于PLL组(8.53±0.84 vs. 1.00±0.12,t = 21.629,P = 0.000)。miR-563过表达导致茜素红染色水平升高(2.52±0.25 vs. 1.00±0.14)、碱性磷酸酶活性升高(3.11±0.55 vs. 1.00±0.11)以及骨化相关基因升高(RUNX2:3.25±0.55 vs. 1.00±0.10;IBSP:2.35±0.32 vs. 1.00±0.14;F = 7.43至10.99,均P = 0.000),而抑制则导致水平降低(茜素红染色:0.52±0.21 vs. 1.00±0.12;碱性磷酸酶活性:0.41±0.12 vs. 1.00±0.09;RUNX2:0.35±0.13 vs. 1.00±0.12;IBSP:0.55±0.12 vs. 1.00±0.11;F = 4.36至8.45,均P < 0.05)。结合Targetscan的预测结果以及OPLL和PLL之间的表达谱,发现SMURF1是miR-563的潜在靶标,双荧光素酶报告基因检测也证实了它们之间的关系。通过过表达,SMURF1的表达水平显著降低(0.25±0.06 vs. 1.00±0.10,t = -12.862,P = 0.000),这再次验证了该假设。miRNA-563显著促进后纵韧带细胞的成骨分化,其机制可能是通过下调SMURF1实现的。