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脂质翻译后修饰对适应性免疫的调控

Regulation of Adaptive Immunity by Lipid Post-translational Modifications.

作者信息

Mattingly Jonathan R, Wu Aimee, York Autumn G

机构信息

Department of Immunology, School of Medicine, University of Washington, Seattle, WA 98195, USA.

出版信息

Immune Netw. 2025 Feb 18;25(1):e11. doi: 10.4110/in.2025.25.e11. eCollection 2025 Feb.

DOI:10.4110/in.2025.25.e11
PMID:40078786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11896658/
Abstract

The burgeoning field of immunometabolism highlights the interdependence between metabolic programs and efficacious immune responses. The current understanding that cellular metabolic remodeling is necessary for a competent adaptive immune response, along with acutely sensitive methodologies such as high-performance liquid chromatography/mass spectrometry and advanced proteomics, have ushered in a renaissance of lipid- and metabolic-based scientific inquiries. One facet of recent interest examines how lipids function as post-translational modifications (PTMs) and their resulting effects on adaptive immune responses. The goal of this review is to establish a fundamental understanding of these protein modifications and highlight recent findings that underscore the importance of continued investigation into lipids as PTMs.

摘要

免疫代谢这一新兴领域凸显了代谢程序与有效免疫反应之间的相互依存关系。目前的认识是,细胞代谢重塑对于有效的适应性免疫反应是必要的,再加上诸如高效液相色谱/质谱和先进蛋白质组学等极其灵敏的方法,引发了基于脂质和代谢的科学探究的复兴。近期研究的一个方面探讨了脂质如何作为翻译后修饰(PTM)发挥作用及其对适应性免疫反应的影响。本综述的目的是建立对这些蛋白质修饰的基本理解,并强调近期的研究结果,这些结果突显了持续研究脂质作为翻译后修饰的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d77a/11896658/4f761b9e4216/in-25-e11-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d77a/11896658/d75662296855/in-25-e11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d77a/11896658/4f761b9e4216/in-25-e11-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d77a/11896658/d75662296855/in-25-e11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d77a/11896658/4f761b9e4216/in-25-e11-g002.jpg

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本文引用的文献

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Palmitoylation of TIM-3 promotes immune exhaustion and restrains antitumor immunity.棕榈酰化 TIM-3 促进免疫衰竭并抑制抗肿瘤免疫。
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mRNA-delivery of IDO1 suppresses T cell-mediated autoimmunity.信使 RNA 投递抑制吲哚胺 2,3-双加氧酶 1 表达可抑制 T 细胞介导的自身免疫。
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Distinct palmitoylation of Foxp3 regulates the function of regulatory T cells via palmitoyltransferases.
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