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感染中巨噬细胞代谢的复杂性

Complexity of macrophage metabolism in infection.

作者信息

He Wei, Heinz Alexander, Jahn Dieter, Hiller Karsten

机构信息

Department for Bioinformatics and Biochemistry, BRICS, Technische Universität Braunschweig, Rebenring 56, 38106 Braunschweig, Germany.

Institute of Microbiology, Technische Universität Braunschweig, Universitätsplatz 2, 38106 Braunschweig, Germany.

出版信息

Curr Opin Biotechnol. 2021 Apr;68:231-239. doi: 10.1016/j.copbio.2021.01.020. Epub 2021 Feb 18.

Abstract

Macrophages are the prominent innate immune cells to combat infection and then restore tissue homeostasis after clearance of pathogens. Intracellular metabolic reprogramming is required for macrophage activation and function, as such adaptations confer macrophages with sufficient energy and metabolites to support biosynthesis and diverse functions. During the last 10 years, knowledge in this field has been greatly extended by outstanding advances demonstrating that several metabolic intermediates possess the ability to directly control macrophage activation and effector functions by various mechanisms. Of note, citrate and succinate contribute to the inflammatory activation of macrophages while tricarboxylic acid cycle-derived metabolite itaconate has a variety of immunomodulatory effects. Such progress not only encourages a further exploration into the emerging new area immunometabolism, but also provides potential therapeutic targets to control unwanted inflammation due to infection.

摘要

巨噬细胞是对抗感染的主要固有免疫细胞,在病原体清除后恢复组织稳态。巨噬细胞的激活和功能需要细胞内代谢重编程,因为这种适应性赋予巨噬细胞足够的能量和代谢物来支持生物合成和各种功能。在过去十年中,该领域的知识因显著进展而得到极大扩展,这些进展表明几种代谢中间体能够通过各种机制直接控制巨噬细胞的激活和效应功能。值得注意的是,柠檬酸和琥珀酸有助于巨噬细胞的炎症激活,而三羧酸循环衍生的代谢物衣康酸具有多种免疫调节作用。这些进展不仅鼓励进一步探索新兴的免疫代谢新领域,还为控制由感染引起的不必要炎症提供了潜在的治疗靶点。

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