Silencing of microRNA-138-5p promotes IL-1β-induced cartilage degradation in human chondrocytes by targeting FOXC1

Objectives Osteoarthritis (OA) is characterised by articular cartilage degradation. MicroRNAs (miRNAs) have been identified in the development of OA. The purpose of our study was to explore the functional role and underlying mechanism of miR-138-5p in interleukin-1 beta (IL-1 beta)induced extracellular matrix (ECM) degradation of OA cartilage. Materials and Methods Human articular cartilage was obtained from patients with and without OA, and chondrocytes were isolated and stimulated by IL-1 beta. The expression levels of miR-138-5p in cartilage and chondrocytes were both determined. After transfection with miR-138-5p mimics, allele-specific oligonucleotide (ASO)-miR-138-5p, or their negative controls, the messenger RNA (mRNA) levels of aggrecan (ACAN), collagen type II and alpha 1 (COL2A1), the protein levels of glycosaminoglycans (GAGs), and both the mRNA and protein levels of matrix metalloproteinase (MMP)-13 were evaluated. Luciferase reporter assay, quantitative real-time polymerase chain reaction (qRT-PCR), and Western blot were performed to explore whether Forkhead Box C1 (FOCX1) was a target of miR-138-5p. Further, we co-transfected OA chondrocytes with miR-138-5p mimics and pcDNA3.1 (+)-FOXC1 and then stimulated with IL-1 beta to determine whether miR-138-5p-mediated IL-1 beta-induced cartilage matrix degradation resulted from targeting FOXC1. Results MiR-138-5p was significantly increased in OA cartilage and in chondrocytes in response to IL-1 beta-stimulation. Overexpression of miR-138-5p significantly increased the IL-1 beta-induced downregulation of COL2A1, ACAN, and GAGs, and increased the IL-1 beta-induced over expression of MMP-13. We found that FOXC1 is directly regulated by miR-138-5p. Additionally, co-transfection with miR-138-5p mimics and pcDNA3.1 (+)-FOXC1 resulted in higher levels of COL2A1, ACAN, and GAGs, but lower levels of MMP-13. Conclusion miR-138-5p promotes IL-1 beta-induced cartilage degradation in human chondrocytes, possibly by targeting FOXC1.