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成纤维细胞生长因子21作用于去甲肾上腺素能神经系统可预防流感病毒感染。

FGF21 acting on the noradrenergic nervous system protects against influenza virus infection.

作者信息

Fan Wei, Zhang Yuan, Gautron Laurent, Thomas David G, Stout-Delgado Heather W, Schenck Edward J, Gwatiringa Tadiwanashe, Rajagopalan Kartik N, Mangelsdorf David J, Kliewer Steven A

机构信息

Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390.

Center for Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.

出版信息

Proc Natl Acad Sci U S A. 2025 Sep 30;122(39):e2522045122. doi: 10.1073/pnas.2522045122. Epub 2025 Sep 25.

Abstract

The hormone fibroblast growth factor 21 (FGF21) is induced in murine liver in response to both bacterial and viral infection. In this report, we show that FGF21 is induced by infection with influenza virus in both humans and mice. Mice lacking FGF21 had decreased food intake, body weight, and body temperature compared to wild-type mice following influenza virus inoculation, indicating reduced tolerance to the infection. Conversely, pharmacologic administration of FGF21 after viral infection protected mice against these pathologic changes. Pair feeding studies showed that neither the induction of FGF21 nor the hypothermia was secondary to decreased food intake. Notably, mice selectively lacking FGF21's coreceptor protein, βKlotho, in noradrenergic neurons were also more susceptible to influenza virus infection, including hypothermia. We show that FGF21 acting on noradrenergic neurons, including those in the locus coeruleus region, stimulates energy expenditure and thermogenic gene expression in brown adipose tissue. Our findings reveal an FGF21-regulated neuronal pathway that protects mice against influenza infection and suggest the potential utility of using FGF21 pharmacologically to improve outcomes after influenza infection.

摘要

成纤维细胞生长因子21(FGF21)这种激素在小鼠肝脏中会因细菌和病毒感染而被诱导产生。在本报告中,我们表明FGF21在人类和小鼠中都会因感染流感病毒而被诱导产生。与接种流感病毒后的野生型小鼠相比,缺乏FGF21的小鼠食物摄入量、体重和体温均下降,这表明其对感染的耐受性降低。相反,病毒感染后给予FGF21药物可保护小鼠免受这些病理变化的影响。配对喂养研究表明,FGF21的诱导和体温过低都不是食物摄入量减少的继发结果。值得注意的是,在去甲肾上腺素能神经元中选择性缺乏FGF21的共受体蛋白βKlotho的小鼠,对流感病毒感染(包括体温过低)也更易感。我们表明,作用于去甲肾上腺素能神经元(包括蓝斑区域的神经元)的FGF21会刺激棕色脂肪组织中的能量消耗和产热基因表达。我们的研究结果揭示了一条FGF21调节的神经元通路,该通路可保护小鼠免受流感感染,并提示了药理学使用FGF21改善流感感染后结局的潜在效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b434/12501196/a60ea2baa265/pnas.2522045122fig01.jpg

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