Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.
Department of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN.
J Immunol. 2023 Feb 15;210(4):359-368. doi: 10.4049/jimmunol.2200467.
Macrophages are sentinels of the innate immune system that maintain tissue homeostasis and contribute to inflammatory responses. Their broad scope of action depends on both functional heterogeneity and plasticity. Small noncoding RNAs called microRNAs (miRNAs) contribute to macrophage function as post-transcriptional inhibitors of target gene networks. Genetic and pharmacologic studies have uncovered genes regulated by miRNAs that control macrophage cellular programming and macrophage-driven pathology. miRNAs control proinflammatory M1-like activation, immunoregulatory M2-like macrophage activation, and emerging macrophage functions in metabolic disease and innate immune memory. Understanding the gene networks regulated by individual miRNAs enhances our understanding of the spectrum of macrophage function at steady state and during responses to injury or pathogen invasion, with the potential to develop miRNA-based therapies. This review aims to consolidate past and current studies investigating the complexity of the miRNA interactome to provide the reader with a mechanistic view of how miRNAs shape macrophage behavior.
巨噬细胞是先天免疫系统的哨兵,维持组织内稳态并参与炎症反应。它们广泛的作用取决于功能异质性和可塑性。称为 microRNAs(miRNAs)的小非编码 RNA 作为靶基因网络的转录后抑制剂,有助于巨噬细胞的功能。遗传和药理学研究已经揭示了受 miRNAs 调控的基因,这些基因控制着巨噬细胞的细胞编程和巨噬细胞驱动的病理学。miRNAs 控制促炎 M1 样激活、免疫调节 M2 样巨噬细胞激活以及代谢疾病和先天免疫记忆中的新兴巨噬细胞功能。了解单个 miRNAs 调控的基因网络,有助于我们理解在稳态和应对损伤或病原体入侵时,巨噬细胞功能的范围,并有可能开发基于 miRNA 的治疗方法。本综述旨在整合过去和当前研究,以探讨 miRNA 相互作用组的复杂性,为读者提供一个关于 miRNA 如何塑造巨噬细胞行为的机制观点。