Progranulin 通过增强自噬减轻炎症反应,从而预防烟曲霉角膜炎

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-08-09 Epub Date: 2024-06-20 DOI:10.1021/acsinfecdis.4c00236
Pingli Qi, Xing Liu, Cui Li, Qiang Xu, Liting Hu, Huijin Duan, Guiqiu Zhao, Jing Lin
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引用次数: 0

摘要

真菌性角膜炎(FK)是由致病真菌引起的一种严重角膜病,与真菌的毒性和过度的组织炎症反应有关。Progranulin(PGRN)作为一种多功能生长因子,对炎症和自噬的调控有着举足轻重的影响。我们的研究旨在分析 PGRN 在曲霉菌角膜炎中的作用。我们发现,在曲霉菌角膜炎的小鼠角膜中,PGRN的表达增加。在我们的实验中,用 100 毫微克/毫升的 PGRN 处理患有 FK 的小鼠角膜。在体外,RAW 264.7 细胞在烟曲霉菌刺激前用 10 ng/mL PGRN 处理。研究结果表明,PGRN 能有效缓解小鼠角膜水肿并减少促炎细胞因子的表达。在受刺激的 RAW 264.7 细胞中,PGRN 处理抑制了促炎细胞因子 IL-6 和 TNF-α 的表达,但促进了抗炎细胞因子 IL-10 的表达。PGRN 处理可明显上调自噬相关蛋白 LC3、Beclin-1 和 Atg-7 的表达。3-甲基腺嘌呤(3-MA,自噬抑制剂)逆转了 PGRN 对炎症细胞因子的调节作用。此外,我们的研究还表明,PGRN 还能增强 RAW 264.7 细胞的吞噬能力。总之,PGRN 通过增加自噬减轻了烟曲霉菌角膜炎的炎症反应,并增强了 RAW 264.7 细胞的吞噬活性。这表明 PGRN 对烟曲霉菌角膜炎有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Progranulin Protects against <i>Aspergillus fumigatus</i> Keratitis by Attenuating the Inflammatory Response through Enhancing Autophagy.

Progranulin Protects against Aspergillus fumigatus Keratitis by Attenuating the Inflammatory Response through Enhancing Autophagy.

Fungal keratitis (FK) is a severe corneal condition caused by pathogenic fungi and is associated with the virulence of fungi and an excessive tissue inflammatory response. Progranulin (PGRN), functioning as a multifunctional growth factor, exerts a pivotal influence on the regulation of inflammation and autophagy. The aim of our research was to analyze the role of PGRN in Aspergillus fumigatus (A. fumigatus) keratitis. We found that PGRN expression was increased in the mouse cornea with A. fumigatus keratitis. In our experiments, corneas of mice with FK were treated with 100 ng/mL of PGRN. In vitro, RAW 264.7 cells were treated with 10 ng/mL of PGRN before A. fumigatus stimulation. The findings suggested that PGRN effectively alleviated corneal edema and decreased the expression of pro-inflammatory cytokines in mice. In stimulated RAW 264.7 cells, PGRN treatment suppressed the expression of pro-inflammatory cytokines IL-6 and TNF-α but promoted the expression of the anti-inflammatory cytokines IL-10. PGRN treatment significantly upregulated the expression of autophagy-related proteins LC3, Beclin-1, and Atg-7. 3-Methyladenine (3-MA, autophagy inhibitor) reversed the regulation of inflammatory cytokines by PGRN. In addition, our study demonstrated that PGRN also enhanced phagocytosis in RAW 264.7 cells. In summary, PGRN attenuated the inflammatory response of A. fumigatus keratitis by increasing autophagy and enhanced the phagocytic activity of RAW 264.7 cells. This showed that PGRN had a protective effect on A. fumigatus keratitis.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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