Immunometabolic reprogramming of macrophages: Emerging roles in skeletal muscle regeneration and therapeutic perspectives

IF 12.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Pharmacological research Pub Date : 2026-02-01 Epub Date: 2026-01-21 DOI:10.1016/j.phrs.2026.108109
Si-jing Li , Xing-ling He , Xiao-jiao Zhang , Zi-ru Li , Hui-lin Liu , Yi-hui Zhang , Min-qi Lu , Jia-hui Chen , Xiao-ming Dong , Wen-jie Long , Lu Lu , Zhong-qi Yang , Shi-hao Ni
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引用次数: 0

Abstract

Skeletal muscle regeneration is a complex and strictly regulated process that involves complex interactions between immune cells, muscle-resident progenitor cells, and stromal components. Macrophages play a central role in this process by coordinating immune responses, supporting regeneration, and promoting tissue remodeling through phenotypic transitions that respond to environmental cues. Under physiological conditions, these transitions ensure efficient tissue restoration. However, in pathological settings or conditions such as aging, muscular dystrophy, cancer cachexia, and metabolic disorders, macrophage function becomes dysregulated. This situation often leads to persistent inflammation, excessive fibrosis, and impaired regeneration of muscle tissue. Recent advances in single-cell and spatial transcriptomics technologies have revealed the remarkable heterogeneity of macrophage subpopulations within skeletal muscle. These findings emphasize the importance of immunometabolic programming as a key driver of macrophage plasticity. Shifts in glucose metabolism, oxidative phosphorylation, lipid utilization, and amino acid pathways critically influence the polarization of macrophages and their interactions with surrounding cells. Moreover, metabolic signals from the tissue microenvironment, circulating factors, and muscle-resident cells create a dynamic network of metabolic crosstalk that shapes macrophage behavior. This review provides a comprehensive summary of how macrophage immunometabolism regulates skeletal muscle regeneration in both acute injury and chronic disease. It highlights core metabolic pathways, macrophage-centered intercellular communication, and emerging therapeutic strategies that aim to reprogram macrophage metabolism for a regenerative benefit. In addition, key challenges and future directions for translating these insights into effective interventions for muscle wasting conditions are discussed.
巨噬细胞的免疫代谢重编程:在骨骼肌再生和治疗方面的新作用
骨骼肌再生是一个复杂的、严格调控的过程,涉及免疫细胞、肌内祖细胞和基质成分之间复杂的相互作用。巨噬细胞在这一过程中发挥核心作用,协调免疫反应,支持再生,并通过响应环境线索的表型转变促进组织重塑。在生理条件下,这些转变确保了有效的组织修复。然而,在病理环境或条件下,如衰老、肌肉萎缩、癌症恶病质和代谢紊乱,巨噬细胞功能变得失调。这种情况通常会导致持续的炎症、过度纤维化和肌肉组织再生受损。单细胞和空间转录组学技术的最新进展揭示了骨骼肌内巨噬细胞亚群的显著异质性。这些发现强调了免疫代谢编程作为巨噬细胞可塑性关键驱动因素的重要性。葡萄糖代谢、氧化磷酸化、脂质利用和氨基酸途径的变化严重影响巨噬细胞的极化及其与周围细胞的相互作用。此外,来自组织微环境、循环因子和肌肉驻留细胞的代谢信号创建了一个动态的代谢串扰网络,形成巨噬细胞的行为。本文综述了巨噬细胞免疫代谢在急性损伤和慢性疾病中如何调节骨骼肌再生。它强调了核心代谢途径,以巨噬细胞为中心的细胞间通讯,以及旨在重编程巨噬细胞代谢以获得再生益处的新兴治疗策略。此外,讨论了将这些见解转化为有效干预肌肉萎缩条件的关键挑战和未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
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