Soedono Shindy, Julietta Vivi, Nawaz Hadia, Cho Kae Won
Department of Integrated Biomedical Science, Soonchunhyang University, Cheonan, Korea.
Soonchunhyang Institute of Medi-bio Science (SIMS), Soonchunhyang University, Cheonan, Korea.
J Obes Metab Syndr. 2024 Sep 30;33(3):193-212. doi: 10.7570/jomes24030. Epub 2024 Sep 26.
Adipose tissue macrophages (ATMs) are key regulators of adipose tissue (AT) inflammation and insulin resistance in obesity, and the traditional M1/M2 characterization of ATMs is inadequate for capturing their diversity in obese conditions. Single-cell transcriptomic profiling has revealed heterogeneity among ATMs that goes beyond the old paradigm and identified new subsets with unique functions. Furthermore, explorations of their developmental origins suggest that multiple differentiation pathways contribute to ATM variety. These advances raise concerns about how to define ATM functions, how they are regulated, and how they orchestrate changes in AT. This review provides an overview of the current understanding of ATMs and their updated categorization in both mice and humans during obesity. Additionally, diverse ATM functions and contributions in the context of obesity are discussed. Finally, potential strategies for targeting ATM functions as therapeutic interventions for obesity-induced metabolic diseases are addressed.
脂肪组织巨噬细胞(ATMs)是肥胖状态下脂肪组织(AT)炎症和胰岛素抵抗的关键调节因子,而传统的ATMs的M1/M2分类不足以描述其在肥胖状态下的多样性。单细胞转录组分析揭示了ATMs之间的异质性,这种异质性超出了以往的模式,并确定了具有独特功能的新亚群。此外,对其发育起源的探索表明,多种分化途径导致了ATMs的多样性。这些进展引发了人们对如何定义ATMs功能、它们如何被调节以及它们如何协调AT变化的关注。本综述概述了目前对肥胖期间小鼠和人类ATMs的理解及其更新分类。此外,还讨论了肥胖背景下ATMs的多种功能和作用。最后,探讨了针对ATMs功能作为肥胖诱导的代谢性疾病治疗干预措施的潜在策略。