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CXC chemokine ligand 16 in periodontal diseases: expression in diseased tissues and production by cytokine-stimulated human gingival fibroblasts

机译:牙周疾病中的CXC趋化因子配体16:在患病组织中的表达和细胞因子刺激的人牙龈成纤维细胞的产生

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摘要

Periodontal disease is an inflammatory disorder characterized by the involvement of chemokines that are important for the recruitment of leucocytes. Several cytokines are involved in regulating levels of chemokines in periodontal disease. CXCL16 is a chemokine related to the migration of T helper 1 (Th1) cells and natural killer (NK) cells. In this study, we examined its expression in periodontal tissues. Moreover, we investigated the effects of cytokines on the production of CXCL16 by human gingival fibroblast (HGF). Reverse transcription–polymerase chain reaction (RT–PCR) analysis and immunohistochemistry revealed that CXCL16 and its receptor, CXCR6, were expressed at the mRNA and protein levels in diseased tissues. Proinflammatory cytokines [interleukin (IL)-1β, tumour necrosis factor (TNF)-α and interferon (IFN)-γ] increased the mRNA expression and release of CXCL16 in a dose-dependent manner. Moreover, treatment of HGFs with IFN-γ in combination with IL-1β had a synergistic effect on the production of CXCL16. On the other hand, IL-4 and IL-13 inhibited the IL-1β-induced CXCL16 production by HGFs. Inhibitors of A disintegrin and metalloprotease (ADAM)10 and ADAM17, a recently identified protease of CXCL16, reduced the amount of CXCL16 released from HGFs. These results suggest that the CXCL16 produced by HGFs may be involved in the migration of leucocytes into inflamed tissues, and provide evidence that CXCL16 production is controlled by cytokines in periodontal disease.
机译:牙周疾病是一种炎症性疾病,其特征在于趋化因子的参与对白细胞的募集很重要。几种细胞因子参与调节牙周疾病中趋化因子的水平。 CXCL16是一种与T辅助1(Th1)细胞和自然杀伤(NK)细胞迁移有关的趋化因子。在这项研究中,我们检查了其在牙周组织中的表达。此外,我们调查了细胞因子对人牙龈成纤维细胞(HGF)产生CXCL16的影响。逆转录聚合酶链反应(RT-PCR)分析和免疫组化显示,CXCL16及其受体CXCR6在患病组织中以mRNA和蛋白质水平表达。促炎细胞因子[白介素(IL)-1β,肿瘤坏死因子(TNF)-α和干扰素(IFN)-γ]以剂量依赖性方式增加CXCL16的mRNA表达和释放。此外,用IFN-γ结合IL-1β处理HGF对CXCL16的产生具有协同作用。另一方面,IL-4和IL-13抑制HGF引起的IL-1β诱导的CXCL16产生。 A整联蛋白和金属蛋白酶(ADAM)10和ADAM17(最近确定的CXCL16蛋白酶)的抑制剂减少了从HGF释放的CXCL16的量。这些结果表明,由HGF产生的CXCL16可能参与白细胞向发炎组织的迁移,并提供证据证明CXCL16的产生受牙周疾病中细胞因子的控制。

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