Met-Vision reveals coexisting energetic states in tissue macrophages redistributed by inflammation.

IF 6.1 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2026-08-03 Epub Date: 2026-06-12 DOI:10.1083/jcb.202603170
Adriana Lecourieux, Margot Bardou, Zacarias Garcia, Philippe Bousso
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引用次数: 0

Abstract

The function of tissue-associated macrophages is tightly linked to their energy metabolism. Yet, the diversity of macrophage metabolic profiles coexisting in tissues at homeostasis or during immune challenges is incompletely understood. Here, we introduce Met-Vision, an imaging-based pipeline for single-cell functional profiling and classification of energy metabolism. Across multiple tissue contexts, we identified that macrophages do not adopt a uniform metabolic profile but typically coexist in four discrete metabolic states with distinct dependence on OXPHOS and metabolic plasticity. Inflammation reconfigured the distribution of macrophage metabolic profiles that remained heterogeneous. Notably, inflammation-derived nitric oxide finely tuned the distribution of macrophage energetic states. These findings challenge the view of homogeneous metabolic activation and reveal a layer of metabolic diversity in tissue at steady state and during inflammation. The ability to stratify macrophage energy metabolic profiles with Met-Vision should help guide the development of metabolism-targeted therapies for inflammatory diseases, cancer, and metabolic disorders.

Met-Vision揭示了炎症重新分配的组织巨噬细胞共存的能量状态。
组织相关巨噬细胞的功能与其能量代谢密切相关。然而,巨噬细胞代谢谱的多样性共存的组织在稳态或免疫挑战是不完全了解。在这里,我们介绍Met-Vision,一种基于成像的管道,用于单细胞功能分析和能量代谢分类。在多种组织环境中,我们发现巨噬细胞并不采用统一的代谢谱,而是通常共存于四种不同的代谢状态,分别依赖于OXPHOS和代谢可塑性。炎症重新配置巨噬细胞代谢谱的分布,保持异质性。值得注意的是,炎症衍生的一氧化氮精细地调节了巨噬细胞能量状态的分布。这些发现挑战了同质代谢激活的观点,揭示了组织在稳态和炎症期间的代谢多样性。利用Met-Vision对巨噬细胞能量代谢谱进行分层的能力将有助于指导针对炎症性疾病、癌症和代谢紊乱的代谢靶向治疗的发展。
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
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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