Drvar Vedrana, Ćurko-Cofek Božena, Karleuša Ljerka, Aralica Merica, Rogoznica Marija, Kehler Tatjana, Legović Dalen, Rukavina Daniel, Laskarin Gordana
Clinical Department of Laboratory Diagnostics, University Hospital Centre Rijeka, 51000 Rijeka, Croatia.
Department of Physiology and Immunology, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.
Biomed Rep. 2022 May;16(5):44. doi: 10.3892/br.2022.1527. Epub 2022 Mar 24.
Osteoarthritis (OA) is a chronic joint disease caused by mechanical damage and metabolic factors that support the development of low-grade inflammation. Increased levels of T helper 1 pro-inflammatory cytokines in the serum of OA patients may support granulysin (GNLY) mediated cytotoxicity, which in-turn may contribute to the pathogenesis of OA. In the present study, GNLY expression and cytotoxic/apoptotic mechanisms mediated by GNLY in the peripheral blood of OA patients were assessed. A total of 40 non-obese women (median age of 64 years old) with knee OA, and 40 controls (median age 62 years old) were enrolled in the study. GNLY, IFN-γ and IL-4 expression levels were investigated in peripheral blood lymphocytes (PBLs) using flow cytometry, immunocytochemistry and/or confocal microscopy. Natural killer (NK) GNLY-mediated apoptosis through NK effectors against K-562 targets was analyzed using the PKH-26 18-h cytotoxicity assay. Serum GNLY levels were assessed using ELISA. The percentage of GNLYPBLs was higher in the OA patients than that in the controls due to the increase in the proportions of GNLY cells in the natural killer (NK), T and natural killer T (NKT) subsets. GNLY localization inside exocytotic lysosomal-associated membrane protein-1 granules was ~40% in both groups. However, the intensity of GNLY labeling in PBLs was higher in OA patients than in the controls, and it was supported by the increased expression of IFN-γ relative to IL-4 in NK and T cells from OA patients. The serum GNLY concentration was <0.3 ng/ml in both groups. RC8 anti-GNLY mAb by itself was unable to significantly alter early apoptosis, whereas RC8 anti-GNLY mAb combined with anti-perforin mAb significantly reduced NK-mediated early apoptosis of K-562 targets in the OA patients, whilst not exerting a notable effect in the controls. Anti-perforin mAb by itself did not affect apoptosis significantly. These results suggest that in women with knee OA, GNLY expression in the PBL subsets and GNLY-mediated early apoptosis of K-562 targets are increased compared with the controls and accompanied by intracellular dominance of IFN-γ over IL-4 in NK cells.
骨关节炎(OA)是一种由机械损伤和代谢因素引起的慢性关节疾病,这些因素会促使低度炎症的发展。OA患者血清中促炎细胞因子辅助性T细胞1水平升高可能会支持颗粒溶素(GNLY)介导的细胞毒性作用,而这反过来可能会促进OA的发病机制。在本研究中,评估了OA患者外周血中GNLY的表达以及GNLY介导的细胞毒性/凋亡机制。共有40名非肥胖女性(中位年龄64岁)患有膝骨关节炎,40名对照者(中位年龄62岁)参与了该研究。使用流式细胞术、免疫细胞化学和/或共聚焦显微镜对外周血淋巴细胞(PBL)中的GNLY、干扰素-γ(IFN-γ)和白细胞介素-4(IL-4)表达水平进行了研究。使用PKH-26 18小时细胞毒性试验分析了自然杀伤(NK)细胞通过NK效应分子对K-562靶标的GNLY介导的凋亡。使用酶联免疫吸附测定(ELISA)评估血清GNLY水平。由于自然杀伤(NK)细胞、T细胞和自然杀伤T(NKT)亚群中GNLY细胞比例增加,OA患者中GNLY阳性PBL的百分比高于对照组。两组中GNLY定位于胞吐溶酶体相关膜蛋白-1颗粒内的比例均约为40%。然而,OA患者PBL中GNLY标记的强度高于对照组,并且OA患者NK细胞和T细胞中IFN-γ相对于IL-4表达的增加也支持了这一点。两组血清GNLY浓度均<0.3 ng/ml。单独使用RC8抗GNLY单克隆抗体(mAb)无法显著改变早期凋亡,而RC8抗GNLY mAb与抗穿孔素mAb联合使用可显著降低OA患者中NK介导的K-562靶标的早期凋亡,而在对照组中未产生显著影响。单独使用抗穿孔素mAb对凋亡没有显著影响。这些结果表明,与对照组相比,患有膝骨关节炎的女性外周血淋巴细胞亚群中的GNLY表达以及GNLY介导的K-562靶标的早期凋亡增加,并且NK细胞中IFN-γ在细胞内占主导地位,超过IL-4。