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棕色脂肪为发热提供燃料。

Brown fat fuels the fire in fever.

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

J Lipid Res. 2024 Nov;65(11):100658. doi: 10.1016/j.jlr.2024.100658. Epub 2024 Sep 26.

Abstract

Fever is a host-pathogen defense mechanism in which the immune system drives a physiologic increase in core body temperature. For over 50 years, it has been known that the temperature of brown adipose tissue (BAT) is increased during the febrile response. However, recent studies suggested that the primary thermogenic protein Uncoupling protein 1 in brown adipocytes does not contribute to fever induction in mice, casting doubt about the functional contribution of BAT to fever. In a new set of studies, Li et al. (2024) provide compelling evidence that fatty acid oxidation is markedly increased in BAT in a Salmonella infection model of fever and strongly suggest that metabolic adaptation in BAT may play a critical role in the febrile response. This article re-opens the debate about how thermogenic and metabolic programs in BAT contribute to fever and raises new questions about whether BAT contributes to host defense against pathogens.

摘要

发热是宿主-病原体防御机制之一,免疫系统引起核心体温生理性升高。50 多年来,人们已经知道棕色脂肪组织(BAT)在发热反应期间会增加温度。然而,最近的研究表明,棕色脂肪细胞中的主要产热蛋白解偶联蛋白 1(UCP1)不会促进小鼠发热,这对 BAT 对发热的功能贡献提出了质疑。在一系列新的研究中,Li 等人(2024)提供了令人信服的证据,表明发热的沙门氏菌感染模型中 BAT 中的脂肪酸氧化明显增加,并强烈表明 BAT 的代谢适应可能在发热反应中发挥关键作用。本文重新引发了关于 BAT 的产热和代谢程序如何促进发热的争论,并提出了关于 BAT 是否有助于宿主抵御病原体的新问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/596f/11536056/314081bbd487/gr1.jpg

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