Gu Yanglin, Wang Guangchang, Chen Peng
Department of Orthopedics, the Central Hospital Affiliated to Jiangnan University, No.68, Zhong Shan Road, Wuxi, Jiangsu, 214002, P.R. China.
Department of Orthopedics, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University, Wuxi, Jiangsu, 214000, P.R. China.
Apoptosis. 2025 Feb;30(1-2):320-333. doi: 10.1007/s10495-024-02051-3. Epub 2024 Dec 7.
This study aimed to explore the role of the growth arrest-specific five gene (GAS5) long non-coding RNA (lncRNA) in fibroblast-like synoviocytes (FLSs) during the development of osteoarthritis (OA). A total of 25 OA synovial tissues and nine healthy control tissues were collected, and their GAS5 expression was compared. To confirm GAS5 expression in vitro, interleukin (IL)-1β was used to mimic a cellular OA model based on isolated FLSs. Quantitative polymerase chain reaction revealed higher expression levels of GAS5 in OA samples than in non-OA samples. In vitro, the stimulation of FLSs by IL-1β induced high GAS5 expression. The IL-1β-exposed cells exhibited impaired growth, viability, and antioxidant capacity, as well as increased cell death, production of cellular and lipid ROS, and inflammatory cytokine levels. The expression levels of ferroptosis-related proteins in FLSs were also altered in IL-1β-exposed cells. GAS5 was observed to directly target and inhibit micro-RNA 205, partially reversing the effect of GAS5 silencing on cell proliferation, cell death, oxidative stress, inflammation, and FLS ferroptosis. FLS ferroptosis is recognized to be involved in OA development, and the downregulation of the GAS5 lncRNA exhibits protective effects by suppressing ferroptosis and sponging miR-205 in FLSs in OA, thereby providing a novel strategy for the treatment of OA. The GAS5-miR-205 axis can regulate inflammation and oxidative stress in the FLSs of patients with OA.
本研究旨在探讨生长停滞特异性5基因(GAS5)长链非编码RNA(lncRNA)在骨关节炎(OA)发展过程中对成纤维样滑膜细胞(FLS)的作用。共收集了25例OA滑膜组织和9例健康对照组织,并比较了它们的GAS5表达。为了在体外证实GAS5的表达,使用白细胞介素(IL)-1β基于分离的FLS模拟细胞OA模型。定量聚合酶链反应显示,OA样本中GAS5的表达水平高于非OA样本。在体外,IL-1β刺激FLS诱导GAS5高表达。暴露于IL-1β的细胞生长、活力和抗氧化能力受损,细胞死亡增加,细胞和脂质活性氧生成增加,炎症细胞因子水平升高。暴露于IL-1β的细胞中FLS中铁死亡相关蛋白的表达水平也发生了改变。观察到GAS5直接靶向并抑制微小RNA 205,部分逆转了GAS5沉默对细胞增殖、细胞死亡、氧化应激、炎症和FLS铁死亡的影响。FLS铁死亡被认为参与OA的发展,GAS5 lncRNA的下调通过抑制OA中FLS的铁死亡和吸附miR-205发挥保护作用,从而为OA的治疗提供了一种新策略。GAS5-miR-205轴可调节OA患者FLS中的炎症和氧化应激。