Hsa_circ_0007482 Promotes Proliferation and Differentiation of Chondrocytes in Knee Osteoarthritis.

IF 2.7 4区 医学 Q1 ORTHOPEDICS CARTILAGE Pub Date : 2024-05-15 DOI:10.1177/19476035241250198
Dongjie Hou, Ling Lu, Ran Tao
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Abstract

Objective: Knee osteoarthritis (KOA) is a complex degenerative joint disease and a major cause of joint dysfunction. This study aimed to explore the function of hsa_circ_0007482 on inflammation, proliferation, differentiation, and apoptosis in KOA.

Design: Real-time quantitative polymerase chain reaction (PCR) was performed to detect the expression of circ_0007482, inflammatory factors, and differentiation-related molecules in KOA chondrocytes and interleukin (IL)-1β-stimulated chondrocytes. The correlation between the circ_0007482 expression and inflammatory factors was analyzed by the Pearson method. KOA cell model was established using IL-1β for 24 hours. The proliferation activity of chondrocytes was evaluated by CCK-8 assay, and cell apoptosis rate was assessed by flow cytometry. The downstream miRNA of circ_0007482 was validated using dual-luciferase reporter assay.

Results: The circ_0007482 expression was elevated in both KOA cartilage tissues and IL-1β-treated chondrocytes and positively correlated with inflammatory factors expression. In comparison to the control group, IL-1β treatment diminished chondrocyte proliferation abilities and increased cell apoptosis and inflammatory factors IL-6, IL-8, and tumor necrosis factor (TNF)-α mRNA expression. Inhibition of circ_0007482 partially improved IL-1β-induced inflammatory reaction. Circ_0007482 could negatively regulate the expression of miR-558.

Conclusions: Interfering of circ_0007482 might partially promote cell proliferation and differentiation, while inhibit cell apoptosis to improve joint injury by regulating miR-558 in IL-1β-treated chondrocyte cell model.

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Hsa_circ_0007482 促进膝骨关节炎软骨细胞的增殖和分化
目的:膝关节骨关节炎(KOA)是一种复杂的退行性关节疾病,也是导致关节功能障碍的主要原因。本研究旨在探讨 hsa_circ_0007482 在 KOA 中对炎症、增殖、分化和凋亡的功能:设计:采用实时定量聚合酶链反应(PCR)检测 circ_0007482、炎症因子和分化相关分子在 KOA 软骨细胞和白细胞介素(IL)-1β 刺激的软骨细胞中的表达。用皮尔逊法分析了circ_0007482表达与炎症因子之间的相关性。使用 IL-1β 建立 KOA 细胞模型 24 小时。用 CCK-8 法评估软骨细胞的增殖活性,用流式细胞术评估细胞凋亡率。利用双荧光素酶报告实验验证了 circ_0007482 的下游 miRNA:结果:circ_0007482在KOA软骨组织和IL-1β处理的软骨细胞中的表达均升高,并与炎症因子的表达呈正相关。与对照组相比,IL-1β处理降低了软骨细胞的增殖能力,增加了细胞凋亡和炎症因子IL-6、IL-8和肿瘤坏死因子(TNF)-α mRNA的表达。抑制 circ_0007482 可部分改善 IL-1β 诱导的炎症反应。Circ_0007482能负向调节miR-558的表达:在 IL-1β 处理的软骨细胞模型中,干扰 circ_0007482 可部分促进细胞增殖和分化,同时通过调节 miR-558 抑制细胞凋亡,从而改善关节损伤。
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来源期刊
CARTILAGE
CARTILAGE ORTHOPEDICS-
CiteScore
6.90
自引率
7.10%
发文量
80
期刊介绍: CARTILAGE publishes articles related to the musculoskeletal system with particular attention to cartilage repair, development, function, degeneration, transplantation, and rehabilitation. The journal is a forum for the exchange of ideas for the many types of researchers and clinicians involved in cartilage biology and repair. A primary objective of CARTILAGE is to foster the cross-fertilization of the findings between clinical and basic sciences throughout the various disciplines involved in cartilage repair. The journal publishes full length original manuscripts on all types of cartilage including articular, nasal, auricular, tracheal/bronchial, and intervertebral disc fibrocartilage. Manuscripts on clinical and laboratory research are welcome. Review articles, editorials, and letters are also encouraged. The ICRS envisages CARTILAGE as a forum for the exchange of knowledge among clinicians, scientists, patients, and researchers. The International Cartilage Repair Society (ICRS) is dedicated to promotion, encouragement, and distribution of fundamental and applied research of cartilage in order to permit a better knowledge of function and dysfunction of articular cartilage and its repair.
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