干扰巨噬细胞平衡(M1/M2):氟苯基取代咪唑的抗炎作用机制

IF 4.4 3区 医学 Q2 CELL BIOLOGY Mediators of Inflammation Pub Date : 2024-02-17 DOI:10.1155/2024/9528976
Julia Salvan da Rosa, Eduarda Talita Bramorski Mohr, Tainá Larissa Lubschinski, Guilherme Nicácio Vieira, Thais Andreia Rossa, Marcus Mandolesi Sá, Eduardo Monguilhott Dalmarco
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引用次数: 0

摘要

传统上,治疗炎症的方法主要是抑制炎症介质的产生;然而,许多炎症对这种传统方法并不耐受。最近,研究人员提出了另一种方法来解决这一问题:对与炎症密切相关的细胞进行免疫调节。因此,作为先天性免疫和获得性免疫的关键因素,巨噬细胞被视为开发新药物的另一个目标。在这项工作中,我们测试了氟苯基咪唑对 RAW 264.7 巨噬细胞的抗炎活性和可能的免疫调节作用。我们还评估了该化合物的抗炎效果,通过该化合物能够降低 M1 标志物 TNF-α、IL-6、MCP-1、IL-12p70、IFN-γ 和 TLR4,p65 磷酸化、iNOS 和 COX-2 mRNA 的高水平表达,以及该化合物在没有脂多糖(LPS)刺激的巨噬细胞中不能诱导 M1 标志物的产生,证实了巨噬细胞向 M2 的再极化。此外,氟苯基咪唑还能在 LPS 刺激前增加 M2 标志物 IL-4、IL-13、CD206、细胞凋亡和吞噬水平、精氨酸酶-1 和 FIZZ-1 mRNA 的表达。同样,它也能诱导巨噬细胞产生这些相同的 M2 标志物,而无需用 LPS 进行诱导。这些结果进一步证实了氟苯基咪唑具有重要的抗炎作用,并证明这种作用是由免疫调节活性引起的,它能够引发巨噬细胞从 M1 向 M2a 的再极化。这些事实表明,这种分子可作为一种替代支架,用于开发治疗炎症的新药物,因为在这种药物中,M2a 巨噬细胞具有抗炎和促进再生的特性。
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Interference in Macrophage Balance (M1/M2): The Mechanism of Action Responsible for the Anti-Inflammatory Effect of a Fluorophenyl-Substituted Imidazole
Traditionally, the treatment of inflammatory conditions has focused on the inhibition of inflammatory mediator production; however, many conditions are refractory to this classical approach. Recently, an alternative has been presented by researchers to solve this problem: The immunomodulation of cells closely related to inflammation. Hence, macrophages, a critical key in both innate and acquired immunity, have been presented as an alternative target for the development of new medicines. In this work, we tested the fluorophenyl-imidazole for its anti-inflammatory activity and possible immunomodulatory effect on RAW 264.7 macrophages. We also evaluated the anti-inflammatory effect of the compound, and the macrophage repolarization to M2 was confirmed by the ability of the compound to reduce the M1 markers TNF-α, IL-6, MCP-1, IL-12p70, IFN-γ, and TLR4, the high levels of p65 phosphorylated, iNOS and COX-2 mRNA expression, and the fact that the compound was not able to induce the production of M1 markers when used in macrophages without lipopolysaccharide (LPS) stimulation. Moreover, fluorophenyl-imidazole had the ability to increase the M2 markers IL-4, IL-13, CD206, apoptosis and phagocytosis levels, arginase-1, and FIZZ-1 mRNA expression before LPS stimulation. Similarly, it was also able to induce the production of these same M2 markers in macrophages without being induced with LPS. These results reinforce the affirmation that the fluorophenyl-imidazole has an important anti-inflammatory effect and demonstrates that this effect is due to immunomodulatory activity, having the ability to trigger a repolarization of macrophages from M1 to M2a. These facts suggest that this molecule could be used as an alternative scaffold for the development of a new medicine to treat inflammatory conditions, where the anti-inflammatory and proregenerative properties of M2a macrophages are desired.
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来源期刊
Mediators of Inflammation
Mediators of Inflammation 医学-免疫学
CiteScore
8.70
自引率
0.00%
发文量
202
审稿时长
4 months
期刊介绍: Mediators of Inflammation is a peer-reviewed, Open Access journal that publishes original research and review articles on all types of inflammatory mediators, including cytokines, histamine, bradykinin, prostaglandins, leukotrienes, PAF, biological response modifiers and the family of cell adhesion-promoting molecules.
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