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参与线粒体脂肪酸β-氧化在大黄鱼(Larimichthys crocea)头肾巨噬细胞抗病毒先天免疫反应中的作用。

Involvement of mitochondrial fatty acid β-oxidation in the antiviral innate immune response in head kidney macrophages of large yellow croaker (Larimichthys crocea).

机构信息

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture and Rural Affairs) and Key Laboratory of Mariculture (Ministry of Education), Ocean University of China, 5 Yushan Road, 266003, Qingdao, Shandong, People's Republic of China.

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture and Rural Affairs) and Key Laboratory of Mariculture (Ministry of Education), Ocean University of China, 5 Yushan Road, 266003, Qingdao, Shandong, People's Republic of China.

出版信息

Fish Shellfish Immunol. 2024 Oct;153:109829. doi: 10.1016/j.fsi.2024.109829. Epub 2024 Aug 12.

Abstract

As a vital pathway for cellular energy production, mitochondrial fatty acid β-oxidation (FAO) is essential in regulating immune responses to bacterial pathogens and maintaining intracellular homeostasis in vertebrates. However, the specific role of FAO in antiviral innate immune response in macrophages remains insufficiently understood. In this study, virus infection simulated by poly(I:C) inhibited FAO, as indicated by the reduced expression of FAO-related genes and proteins in the head kidney of large yellow croaker, with similar results observed in poly(I:C)-stimulated macrophages. Then, inhibition of FAO by supplementary mildronate in vivo and etomoxir treatment in vitro revealed varying increases in the mRNA expression of antiviral innate immune response genes after stimulated by poly(I:C) in the head kidney and macrophages. Notably, etomoxir significantly facilitated the transcriptional up-regulation of the IFNh promoter by IRF3. Moreover, inhibiting FAO by knockdown of cpt1b promoted antiviral innate immune response triggered by poly(I:C) in macrophages. Conversely, activating FAO through overexpression of cpt1b or cpt2 significantly reduced the mRNA levels of antiviral response genes in macrophages stimulated by poly(I:C). Unlike etomoxir, cpt1b overexpression inhibited the transcriptional up-regulation of the IFNh promoter by IRF3. Furthermore, in vivo dietary palm oil feeding and in vitro exposure to palmitic acid inhibited the antiviral innate immune response triggered by poly(I:C) in the head kidney and macrophages, respectively. These effects were partly associated with FAO activation, as evidenced by etomoxir. In summary, this study elucidates FAO's critical role in regulating antiviral innate immune response in head kidney macrophages. These findings not only deepen insights into the interaction between metabolic remodeling and host immune responses, but also offer valuable guidance for developing nutritional strategies to improve antiviral immunity in aquaculture.

摘要

作为细胞能量产生的重要途径,线粒体脂肪酸β-氧化(FAO)对于调节对细菌病原体的免疫反应和维持脊椎动物细胞内稳态至关重要。然而,FAO 在巨噬细胞抗病毒先天免疫反应中的具体作用仍知之甚少。在这项研究中,聚肌苷酸(poly(I:C))模拟的病毒感染抑制了 FAO,大黄鱼头部肾脏中 FAO 相关基因和蛋白的表达减少,聚肌苷酸刺激的巨噬细胞中也观察到类似的结果。然后,体内补充米力农和体外使用 etomoxir 抑制 FAO,发现头部肾脏和巨噬细胞在 poly(I:C)刺激后,抗病毒先天免疫反应基因的 mRNA 表达增加。值得注意的是,etomoxir 显著促进了 IRF3 对 IFNh 启动子的转录上调。此外,通过 cpt1b 敲低抑制 FAO 促进了 poly(I:C)刺激的巨噬细胞中的抗病毒先天免疫反应。相反,通过过表达 cpt1b 或 cpt2 激活 FAO 显著降低了 poly(I:C)刺激的巨噬细胞中抗病毒反应基因的 mRNA 水平。与 etomoxir 不同,cpt1b 过表达抑制了 IRF3 对 IFNh 启动子的转录上调。此外,体内棕榈油喂养和体外棕榈酸暴露分别抑制了头部肾脏和巨噬细胞中 poly(I:C)触发的抗病毒先天免疫反应,这与 FAO 的激活有关,如 etomoxir 所证明的。总之,本研究阐明了 FAO 在调节头部肾脏巨噬细胞抗病毒先天免疫反应中的关键作用。这些发现不仅加深了对代谢重塑与宿主免疫反应相互作用的认识,而且为开发营养策略提供了有价值的指导,以提高水产养殖中的抗病毒免疫力。

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