microRNA-1236 promotes chondrocyte apoptosis in osteoarthritis via direct suppression of PIK3R3

被引:23
|
作者
Wang, Wan-Tao [1 ]
Huang, Zhi-Peng [1 ]
Sui, Shi [1 ]
Liu, Jian-Hui [1 ,2 ]
Yu, Da-Miao [1 ,3 ]
Wang, Wen-Bo [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Orthopaed, Harbin 150081, Peoples R China
[2] Chinese Peoples Liberat Army Joint Logist, Support Unit Hosp 962, Dept Orthopaed, Harbin 150081, Peoples R China
[3] First Hosp Yichun City, Dept Orthopaed, Yichun 153000, Heilongjiang, Peoples R China
关键词
Osteoarthritis; miRNA; Chondrocytes; Apoptosis; PATHOGENESIS; MIR-1236;
D O I
10.1016/j.lfs.2020.117694
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: Chondrocyte degeneration is the main cause of osteoarthritis (OA) and increased evidence suggests that miRNAs could have vital roles in the pathology of various cartilage illnesses. miR-1236 has been found to contribute to inflammation in diseases such as pneumonia. However, the exact role of miR-1236 in OA is poorly understood. Materials and methods: H&E staining and saffron fixation experiments were employed to determine OA tissues. qRT-PCR and immunohistochemistry were used to detect the expression levels of miR-1236 and PIK3R3. Western blot was performed to detect the expression levels of proteins. Luciferase reporter assays were utilized to investigate the interaction between miR-1236 and PIK3R3. Cell counting assays and AO/EB were used to quantify cell growth and apoptosis. Key findings: miR-1236 was up-regulated in OA knee cartilage compared to normal cartilage. Up-regulated expression of miR-1236 suppressed cell proliferation as well as induced apoptosis in chondrocytes. Bioinformatics identified PIK3R3 as a target of miR-1236. Co-transfection with miR-1236 and PIK3R3 could reverse cell apoptosis induced by the miR-1236 mimic. Significance: These data enhance our understanding on the role of miR-1236 in OA and identifies miR-1236 as a potential biomarker or possible treatment target within OA.
引用
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页数:7
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