羟氯喹对人原代软骨细胞和髓核培养中HDAC活性的影响。

Yasin Emre Kaya, Numan Karaarslan, Ibrahim Yilmaz, Tamer Tamdogan, Sevim Ondul, Duygu Yasar Sirin, Hanefi Ozbek
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引用次数: 0

摘要

目的:研究羟基氯喹(HCQ)对体外大鼠组蛋白去乙酰化酶(HDAC)酶活性及白细胞介素(IL)-6、IL-10、肿瘤坏死因子-α (TNF-α)表达的影响。在HDAC抑制剂丙戊酸存在的情况下,在两种不同组织制备的人原代细胞培养物中测试了HDAC酶活性和炎症标志物的表达。材料和方法:制备原代细胞培养物。未接受任何药物治疗的样本为对照组,经HCQ处理的培养样本为研究组。采用吉姆萨染色法和倒置光镜观察细胞表面形态和细胞外基质(ECM)。采用3-(4,5-二甲基噻唑-2 -基)-2,5-二苯基溴化四唑(MTT)检测细胞活力、增殖和细胞毒性。同时用吖啶橙(AO)/碘化丙啶(PI)染色,并在荧光显微镜下观察。使用商业酶联免疫吸附测定试剂盒评估HDAC酶活性和IL-6、IL-10和TNF-α的表达。采用统计学方法对所得数据进行分析。α显著性水平为p 0.05。结果:HCQ在测试剂量和持续时间下应用于细胞培养,对细胞活力、增殖和细胞或ECM形态有细胞毒性作用。它增加软骨细胞中HDAC活性,引起促炎反应,细胞中TNF-α升高(p 0.05)。结论:综上所述,HCQ具有提高HDAC活性的细胞毒作用;因此,在临床使用HCQ时应考虑到这种促炎反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Effects of HDAC Activity in Hydroxychloroquine Applied Human Primary Chondrocyte and Nucleus Pulposus Cultures.

Aim: To evaluate the in vitro effects of hydroxychloroquine (HCQ) on histone deacetylase (HDAC) enzyme activity and interleukin (IL)-6, IL-10, and tumor necrosis factor-alpha (TNF-α) expressions.

Material and methods: Primary cell cultures were prepared. Samples that did not receive any medication constituted the control group, while culture samples treated with HCQ served as the study group. The surface morphology of cells and the extracellular matrix (ECM) were evaluated by Giemsa staining and inverted light microscopy. Cell viability, proliferation, and cytotoxicity were determined by 3-(4,5-dimethylthiazol2-yl)-2,5-diphenyltetrazolium-bromide (MTT) analysis. The cultures were simultaneously stained with acridine orange (AO)/propidium iodide (PI) and viewed under fluorescence microscopy. HDAC enzyme activity and IL-6, IL-10, and TNF-α expression were evaluated using commercial enzyme-linked immunosorbent assay kits. The obtained data were analyzed using statistical methods. The alpha significance level was accepted as p < 0.05.

Results: HCQ applied to cell cultures at the tested doses and durations showed cytotoxic effects on cell viability, proliferation, and cell or ECM morphology. It increased HDAC activity in chondrocytes and caused a proinflammatory response, indicated by an increase in TNF-α in the cells (p < 0.05).

Conclusion: The results of this study emphasized that the cytotoxic effect of HCQ increased HDAC activity; therefore, this proinflammatory response should be taken into consideration in the clinical use of HCQ.

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