Knockdown of hsa_circ_0037658 inhibits the progression of osteoarthritis via inducing autophagy

被引:16
|
作者
Sui, Cong [1 ]
Liu, Debao [1 ]
Que, Yukang [1 ]
Xu, Shenglin [1 ]
Hu, Yong [1 ]
机构
[1] Anhui Med Univ, Dept Orthopaed, Affiliated Hosp 1, 218 Jixi Rd, Hefei 230022, Anhui, Peoples R China
关键词
OA; hsa_circ_0037658; Autophagy; LONG NONCODING RNA; CHONDROCYTE APOPTOSIS; PROLIFERATION; INJURY;
D O I
10.1007/s13577-020-00440-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteoarthritis (OA) is a chronic musculoskeletal degeneration disease that can result in chronic pain and functional disability. Circular RNAs (CirRNAs) are known to be involved in OA. It was reported that hsa_circ_0037658 was notably upregulated in OA tissues; however, the biological role of hsa_circ_0037658 in OA remains unclear. To investigate the function of hsa_circ_0037658 in OA, CHON-001 cells were treated with IL-1 beta. The effect of hsa_circ_0037658 knockdown on cell growth was tested by CCK-8 and immunofluorescence staining. In addition, the correlation between hsa_circ_0037658 and autophagy was explored by LC3 staining and western blot. The results indicated that hsa_circ_0037658 was significantly upregulated in IL-1 beta-treated CHON-001 cells. The silencing of hsa_circ_0037658 could protect CHON-001 cell injury against IL-1 beta. Moreover, hsa_circ_0037658 shRNA reversed IL-1 beta-induced cell growth inhibition via inducing cell autophagy. Furthermore, knockdown of hsa_circ_0037658 notably alleviated the symptom of OA in vivo. To sum up, knockdown of hsa_circ_0037658 suppressed the progression of OA via inducing autophagy. Thus, hsa_circ_0037658 might serve as a potential target for the treatment of OA.
引用
收藏
页码:76 / 85
页数:10
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