巨噬细胞免疫代谢:衰老肌肉再生的新靶点。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM American journal of physiology. Endocrinology and metabolism Pub Date : 2025-02-01 Epub Date: 2025-01-06 DOI:10.1152/ajpendo.00403.2024
Zachary J Fennel, Ryan M O'Connell, Micah J Drummond
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引用次数: 0

摘要

肌肉萎缩的恢复随着年龄的增长而受损,其特征是不适当的肌肉重塑和持续的功能缺陷。与年龄相关的肌肉再生缺陷与早期促炎巨噬细胞反应的丧失和随后骨骼肌生态位内细胞失调密切相关。巨噬细胞炎症表型在代谢水平上受到调节,强调免疫代谢是增强巨噬细胞反应和恢复功能性肌肉再生的新兴策略。因此,强调糖酵解、缺氧和氧化还原相关途径的代谢靶点在促进巨噬细胞炎症和促进衰老过程中肌肉再生方面的作用突出。在这里,我们强调了有希望的免疫代谢靶点,这些靶点可以用来恢复衰老过程中促炎巨噬细胞的最佳功能,并增强肌肉萎缩后的肌肉再生。
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Macrophage immunometabolism: emerging targets for regrowth in aging muscle.

The recovery from muscle atrophy is impaired with aging as characterized by improper muscle remodeling and sustained functional deficits. Age-related deficits in muscle regrowth are tightly linked with the loss of early pro-inflammatory macrophage responses and subsequent cellular dysregulation within the skeletal muscle niche. Macrophage inflammatory phenotype is regulated at the metabolic level, highlighting immunometabolism as an emerging strategy to enhance macrophage responses and restore functional muscle regrowth. Accordingly, metabolic targets with an emphasis on glycolytic, hypoxia, and redox-related pathways stand out for their role in promoting macrophage inflammation and enhancing muscle regrowth in aging. Here we highlight promising immuno-metabolic targets that could be leveraged to restore optimal pro-inflammatory macrophage function in aging and enhance muscle regrowth following muscular atrophy.

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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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