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马尿酸 1 调节烟曲霉菌角膜炎中性粒细胞募集和白细胞介素 10 表达。

Maresin1 regulates neutrophil recruitment and IL-10 expression in Aspergillus fumigatus keratitis.

机构信息

Department of Ophthalmology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, China.

Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, China.

出版信息

Int Immunopharmacol. 2019 Apr;69:103-108. doi: 10.1016/j.intimp.2019.01.032. Epub 2019 Jan 25.

Abstract

PURPOSE

Maresin1, a lipid mediator derived from polyunsaturated fatty acids, has been shown to suppress the inflammatory response in various inflammatory diseases. However, its effects in fungal keratitis are still uncertain. In this study, we investigated the role of maresin1 (MaR1) in Aspergillus fumigatus keratitis of the eye in a mouse model.

METHODS

Mouse corneas were infected with A. fumigatus by corneal intrastromal injection. Two hours after infection, maresin1 (5 ng/5 μl) was delivered by subconjunctival injection. Then, topical administration of maresin1 (5 ng/3 μl) was applied to mouse corneas twice a day from day 1 to day 5. The development of FK lesions, the production of chemokines, the production of inflammation cytokines and the levels of p-GSK3β were measured via slit-lamp biomicroscope, quantitative polymerase chain reaction (qRT-PCR) and western blot. The presence of neutrophils in the cornea was detected by immunofluorescence staining and myeloperoxidase. The effect of maresin1 on A. fumigatus stimulated mouse macrophage RAW264.7 cells was assessed via PCR and Western blot.

RESULTS

In our study, administration of maresin1 reduced the severity of fungal keratitis with infiltration of fewer neutrophils and reduced levels of the chemokine CXCL1, while the anti-inflammatory cytokines such as IL-10 were enhanced compared with the PBS group. Additionally, in vitro studies showed that treatment with maresin1 inhibited the production of the chemokine CXCL1 and enhanced IL-10 levels in A. fumigatus stimulated RAW264.7 mouse macrophages. Moreover, levels of p-GSK3β increased after maresin1 treatment in A. fumigatus stimulated RAW264.7 cells.

CONCLUSION

Taken together, these findings demonstrate that treatment with maresin1 moderates corneal inflammation through reducing neutrophil recruitment and levels of the chemokine CXCL1 and enhancing the anti-inflammatory cytokine IL-10 in A. fumigatus keratitis. Additionally, maresin1 alters levels of GSK3β phosphorylation to regulate CXCL1 and IL-10 expression in response to A. fumigatus infection. Topical administration of maresin1 may emerge as a novel anti-inflammatory molecule and has a protective role in A. fumigatus keratitis.

摘要

目的

maresin1 是一种源自多不饱和脂肪酸的脂质介质,已被证明可抑制各种炎症性疾病中的炎症反应。然而,其在真菌性角膜炎中的作用尚不确定。在这项研究中,我们在小鼠模型中研究了 maresin1(MaR1)在烟曲霉菌角膜炎中的作用。

方法

通过角膜基质内注射将 A. fumigatus 感染小鼠角膜。感染后 2 小时,通过结膜下注射给予 maresin1(5ng/5μl)。然后,从第 1 天到第 5 天,每天两次通过眼表面给药将 maresin1(5ng/3μl)施用于小鼠角膜。通过裂隙灯生物显微镜、定量聚合酶链反应(qRT-PCR)和 Western blot 测量 FK 病变的发展、趋化因子的产生、炎症细胞因子的产生和 p-GSK3β 的水平。通过免疫荧光染色和髓过氧化物酶检测角膜中的中性粒细胞。通过 PCR 和 Western blot 评估 maresin1 对 A. fumigatus 刺激的小鼠巨噬细胞 RAW264.7 细胞的作用。

结果

在我们的研究中,与 PBS 组相比,给予 maresin1 可减轻真菌性角膜炎的严重程度,减少中性粒细胞浸润,并降低趋化因子 CXCL1 的水平,同时增强抗炎细胞因子如 IL-10 的水平。此外,体外研究表明,用 maresin1 治疗可抑制 A. fumigatus 刺激的 RAW264.7 小鼠巨噬细胞中趋化因子 CXCL1 的产生,并提高 IL-10 水平。此外,在 A. fumigatus 刺激的 RAW264.7 细胞中用 maresin1 处理后,p-GSK3β 的水平增加。

结论

综上所述,这些发现表明,用 maresin1 治疗可通过减少中性粒细胞募集和趋化因子 CXCL1 的水平并增强真菌性角膜炎中的抗炎细胞因子 IL-10 来调节角膜炎症。此外,maresin1 改变 GSK3β 磷酸化水平以调节对 A. fumigatus 感染的 CXCL1 和 IL-10 表达。局部给予 maresin1 可能成为一种新型抗炎分子,并在 A. fumigatus 角膜炎中具有保护作用。

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