Yin Jichao, Zhuang Guihua, Zhu Yi, Hu Xinglv, Zhao Hongmou, Zhang Rongqiang, Guo Hao, Fan Xiaochen, Cao Yi
Department of Epidemiology and Biostatistics, School of Public Health, Xi'an Jiaotong University Health Science Center, No. 76 West Yanta Road, Xi'an, Shaanxi, 710061, China.
Department of Orthopedics and Traumatology, Xi'an Hospital of Traditional Chinese Medicine, Xi'an, China.
Cell Biol Int. 2017 Jul;41(7):779-786. doi: 10.1002/cbin.10780. Epub 2017 May 11.
Ossification of the ligamentum flavum (OLF) is a disease of heterotopic ossification in spinal ligaments. The key of the OLF pathogenesis is the differentiation of fibroblasts into osteoblasts. In this study, we explored the role of miR-615-3p in the osteogenic differentiation of human LF cells. The expression of miR-615-3p was detected during the osteogenic differentiation of hFOB1.19 human osteoblasts, human BMSCs, and human LF cells. The qPCR results showed that miR-615-3p was being decreased during the osteogenic differentiation of these cell lineages. Then, both gain- and loss-function experiments, respectively performed by single-strand miR-615-3p mimic and antagomir, revealed that miR-615-3p negatively regulated the osteogenesis of hLF cells, manifested by a lighter staining degree with Alizarin Red and a decreased level of osteogenic marker genes, including alkaline phosphatase (ALP), RUNX2, osterix (ostx), osteocalcin (OCN), and osteopontin (OPN). Subsequently, our data on bioinformatic analysis, 3'-UTR luciferase activity assay, and protein level detection indicated that miR-615-3p directly targeted and suppressed the expression of FOXO1 and GDF5. Furthermore, knockdown of either FOXO1 or GDF5 could inhibit the osteogenic differentiation of hLF cells, which displayed a similar effect with the miR-615-3p mimic. In conclusion, miR-615-3p negatively regulates the osteogenic differentiation of hLF cells through post-transcriptionally suppressing osteogenic regulators GDF5 and FOXO1. It can be regarded as a potential target for human OLF therapy.
黄韧带骨化(OLF)是一种脊柱韧带异位骨化疾病。OLF发病机制的关键在于成纤维细胞向成骨细胞的分化。在本研究中,我们探讨了miR-615-3p在人黄韧带细胞成骨分化中的作用。在hFOB1.19人成骨细胞、人骨髓间充质干细胞和人黄韧带细胞的成骨分化过程中检测了miR-615-3p的表达。qPCR结果显示,在这些细胞谱系的成骨分化过程中,miR-615-3p表达降低。然后,分别通过单链miR-615-3p模拟物和拮抗剂进行的功能获得和功能丧失实验表明,miR-615-3p负向调节hLF细胞的成骨作用,表现为茜素红染色程度较轻,以及包括碱性磷酸酶(ALP)、RUNX2、osterix(ostx)、骨钙素(OCN)和骨桥蛋白(OPN)在内的成骨标记基因水平降低。随后,我们的生物信息学分析、3'-UTR荧光素酶活性测定和蛋白质水平检测数据表明,miR-615-3p直接靶向并抑制FOXO1和GDF5的表达。此外,敲低FOXO1或GDF5均可抑制hLF细胞的成骨分化,其效果与miR-615-3p模拟物相似。总之,miR-615-3p通过转录后抑制成骨调节因子GDF5和FOXO1负向调节hLF细胞的成骨分化。它可被视为人类OLF治疗的潜在靶点。