你吃什么就是什么:自噬通过代谢引导CD8+ T细胞的功能。

Immunometabolism (Cobham (Surrey, England)) Pub Date : 2025-06-26 eCollection Date: 2025-07-01 DOI:10.1097/IN9.0000000000000064
Caio Loureiro Salgado, Henrique Borges da Silva
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引用次数: 0

摘要

幼稚CD8+ T细胞分化为效应或记忆群体需要细胞代谢和蛋白质组组成的动态重塑。在最近发表在Nature Immunology上的一项研究中,Sinclair等人对自噬,特别是自噬在CD8+ T细胞分化过程中调节这些过程中的作用提供了重要的见解。自噬是一种保守的分解代谢机制,传统上认为它与营养缺乏时细胞的稳态和存活有关。相反,Sinclair等人发现,在免疫系统中,自噬不仅仅是一种生存机制,而是一种对CD8+ T细胞代谢和功能的微调调节,微调CD8+ T细胞效应与静止的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
You are what you eat: autophagy guides CD8+ T cell function through metabolism.

The differentiation of naive CD8+ T cells into effector or memory populations requires dynamic remodeling of cellular metabolism and proteome composition. In a recent study published in Nature Immunology, Sinclair et al offer critical insights into the role of autophagy, particularly mitophagy, in regulating these processes during CD8+ T cell differentiation. Autophagy, a conserved catabolic mechanism, is traditionally associated with cellular homeostasis and survival during nutrient deprivation. In contrast, Sinclair et al reveal that, in the immune system, autophagy is not simply a survival mechanism but a fine-tuned regulator of CD8+ T cell metabolism and function, fine-tuning CD8+ T cell effector vs quiescence choices.

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