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环状 RNA 114876 通过靶向 miR-671/TRAF2 轴促进 IL-1β 诱导的软骨细胞损伤。

Circ_0114876 promoted IL-1β-induced chondrocyte injury by targeting miR-671/TRAF2 axis.

机构信息

Institute of Orthopedic Diseases and Center for Joint Surgery and Sports Medicine, The First Affiliated Hospital of Jinan University, No. 613 Huangpu Avenue West, Tianhe District, Guangzhou, 510630, PR China.

出版信息

Biotechnol Lett. 2021 Apr;43(4):791-802. doi: 10.1007/s10529-020-03070-1. Epub 2021 Jan 6.

Abstract

Osteoarthritis (OA) is a chronic joint disease, which occurs in the elderly. The regulatory mechanisms of circRNAs were involved in the occurrence and development of various diseases. However, the potential regulatory network of circRNA in OA remains further research and clarification. The expression of circ_0114876 was increased in OA tissues and inhibition of circ_0114876 could induce cell viability and suppress inflammation as well as inhibit cell apoptosis in IL-1β induced CHON-001 cells. Circ_0114876 regulated TRAF2 expression via sponging miR-671 in CHON-001 cells. Down-regulated miR-671 expression could reverse the effects of low circ_0114876 expression on cell progression and inflammation in IL-1β induced CHON-001 cells. Overexpression of TRAF2 could weaken the promotion effects of high miR-671 expression on cell progression and inflammation in IL-1β induced CHON-001 cells. Circ_0114876 targeted miR-671 to regulate cell progression and inflammation via modulating TRAF2 expression in IL-1β induced CHON-001 cells, and played an important regulatory mechanism in IL-1β-induced chondrocyte injury, providing a novel diagnostics and therapeutics in OA.

摘要

骨关节炎(OA)是一种慢性关节疾病,发生于老年人。circRNAs 的调控机制参与了各种疾病的发生和发展。然而,circRNA 在 OA 中的潜在调控网络仍需要进一步研究和阐明。circ_0114876 在 OA 组织中的表达增加,抑制 circ_0114876 可诱导细胞活力,并抑制 IL-1β诱导的 CHON-001 细胞中的炎症和细胞凋亡。circ_0114876 通过海绵吸附 miR-671 调控 TRAF2 在 CHON-001 细胞中的表达。下调 miR-671 表达可逆转低 circ_0114876 表达对 IL-1β诱导的 CHON-001 细胞中细胞进展和炎症的影响。过表达 TRAF2 可削弱高 miR-671 表达对 IL-1β诱导的 CHON-001 细胞中细胞进展和炎症的促进作用。circ_0114876 通过调节 TRAF2 在 IL-1β诱导的 CHON-001 细胞中的表达,靶向 miR-671 调控细胞进展和炎症,在 IL-1β诱导的软骨细胞损伤中发挥重要的调控机制,为 OA 的诊断和治疗提供了新的策略。

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