Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary.
Institute of Pharmaceutical Chemistry and Research Group for Stereochemistry, Hungarian Academy of Sciences, University of Szeged, Szeged, Hungary.
Front Immunol. 2019 Jun 21;10:1406. doi: 10.3389/fimmu.2019.01406. eCollection 2019.
The investigation of anti-inflammatory and immunosuppressive functions of Kynurenic acid (KYNA) is now in focus. There is also substantial evidence that TSG-6 has an anti-inflammatory activity. Therefore, in the present study, we compared the effects of newly synthetized KYNA analogs on the TNF-α production in U-937 monocytic cells in correlation with the effects on the TSG-6 expression. TNF-α production was measured by ELISA, the TSG-6 expression was determined by RTqPCR method. As cytokine inducers and were used. KYNA and KYNA analogs attenuated TNF-α production and increased TSG-6 mRNA expression in U-937 cells stimulated by heat inactivated . In contrast, KYNA and some of the KYNA analogs increased the TNF-α production of infected U-937 cells; however, the newly synthetized analogs (SZR104, SZR 105, and SZR 109) exerted significant inhibitory effects on the TNF-α synthesis. The inhibitory and stimulatory effects correlated inversely with the TSG-6 expression. TSG-6 expression following activation with bacterial components could participate in the suppression of inflammatory cytokines, such as TNF-α, We suppose that the elevation of the TSG-6 expression by KYNA and especially by new KYNA analogs might be one of the mechanisms that are responsible for their suppressive effect on TNF-α production as a feedback mechanism. KYNA and KYNA analogs have an important role in influencing TSG-6 expression, and there is a possible benefit of targeting TSG-6 expression by kynurenines in inflammatory conditions following infections.
现在,人们对犬尿酸(KYNA)的抗炎和免疫抑制功能的研究正成为焦点。有大量证据表明 TSG-6 具有抗炎活性。因此,在本研究中,我们比较了新合成的 KYNA 类似物对 U-937 单核细胞中 TNF-α 产生的影响,并与对 TSG-6 表达的影响相关联。通过 ELISA 测量 TNF-α 的产生,通过 RTqPCR 方法确定 TSG-6 的表达。使用 和 作为细胞因子诱导剂。热灭活的 刺激 U-937 细胞时,KYNA 和 KYNA 类似物可减弱 TNF-α 的产生并增加 TSG-6 mRNA 的表达。相反,KYNA 和某些 KYNA 类似物增加了 感染的 U-937 细胞中 TNF-α 的产生;然而,新合成的类似物(SZR104、SZR 105 和 SZR 109)对 TNF-α 的合成具有显著的抑制作用。抑制和刺激作用与 TSG-6 的表达呈负相关。与细菌成分激活后 TSG-6 的表达可能参与抑制炎症细胞因子(如 TNF-α)。我们假设 KYNA 上调 TSG-6 的表达,特别是通过新的 KYNA 类似物,可能是其抑制 TNF-α 产生的机制之一,作为一种反馈机制。KYNA 和 KYNA 类似物在影响 TSG-6 表达方面具有重要作用,在感染后炎症条件下,通过犬尿氨酸靶向 TSG-6 表达可能具有潜在的益处。