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胞葬作用中的代谢重编程

Metabolic reprogramming in efferocytosis.

作者信息

Yan Qing, Li Kuo, Chen Lu, Wang Aowei, Xi Yingying, Xiao Hui, Yuan Lei

机构信息

College of Life Sciences, Shaanxi Normal University, Xi'an, China.

Department of Human Anatomy and Histoembryology, School of Basic Medical Science, Ningxia Medical University, Yinchuan, China.

出版信息

Front Cell Dev Biol. 2025 Sep 10;13:1677028. doi: 10.3389/fcell.2025.1677028. eCollection 2025.

Abstract

Efferocytosis refers to the process by which phagocytes specifically identify and eliminate apoptotic cells. This process is essential for both maintaining tissue homeostasis and suppressing inflammatory responses, as well as facilitating tissue repair. When phagocytes internalize apoptotic cells, which act as "nutrient packages," they undergo significant metabolic reprogramming. This reprogramming not only supplies energy and biosynthetic precursors necessary for engulfment but also critically influences the functional phenotype of phagocytes through complex molecular networks. These networks ultimately determine whether phagocytes adopt an anti-inflammatory resolution or a pathological pro-inflammatory state. This article offers a comprehensive analysis of the molecular regulatory mechanisms that underpin metabolic reprogramming during efferocytosis, aiming to elucidate the intricate regulatory networks formed by the interaction of metabolites as signaling molecules and classical signaling pathways. We examine how the three primary metabolic pathways-glucose, lipid, and amino acid metabolisms-are regulated by signals from efferocytosis and, in turn, modulate phagocyte function. A deeper understanding of the interplay between metabolic reprogramming and efferocytosis will provide a theoretical foundation and novel targets for treating diseases associated with impaired clearance of apoptotic cells.

摘要

胞葬作用是指吞噬细胞特异性识别并清除凋亡细胞的过程。这一过程对于维持组织稳态、抑制炎症反应以及促进组织修复都至关重要。当吞噬细胞内化作为“营养包”的凋亡细胞时,它们会经历显著的代谢重编程。这种重编程不仅提供吞噬所需的能量和生物合成前体,还通过复杂的分子网络严重影响吞噬细胞的功能表型。这些网络最终决定吞噬细胞是采取抗炎消退还是病理性促炎状态。本文对胞葬作用过程中代谢重编程的分子调控机制进行了全面分析,旨在阐明代谢物作为信号分子与经典信号通路相互作用形成的复杂调控网络。我们研究了葡萄糖、脂质和氨基酸这三种主要代谢途径如何受到胞葬作用信号的调节,进而调节吞噬细胞功能。对代谢重编程与胞葬作用之间相互作用的更深入理解将为治疗与凋亡细胞清除受损相关疾病提供理论基础和新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d87/12457674/ec439c8130eb/fcell-13-1677028-g001.jpg

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