探索代谢应激条件下 IL-6 和 IL- 1β 对 M2 巨噬细胞的作用机制和相互影响。

IF 3.7 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shawna Yadav, Anusha Prasannan, Kaliyamurthi Venkatachalam, Ambika Binesh
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引用次数: 0

摘要

巨噬细胞是高度可变的免疫细胞,在控制炎症和维持组织平衡中起重要作用。分化为两种主要类型的能力——m1,促进炎症,M2,解决炎症和促进组织修复——决定了它们在健康和疾病中的特定作用。M2巨噬细胞在减少炎症和促进组织再生方面尤为重要,但其功能主要由周围细胞决定。这在肥胖、糖尿病和慢性炎症中很明显。虽然许多细胞因子调节巨噬细胞极化,但白细胞介素-6 (IL-6)和白细胞介素-1β (IL-1β)是主要的参与者,但它们在代谢应激下对M2巨噬细胞行为的影响尚不清楚。本研究描述了代谢应激下M2巨噬细胞中IL-6和IL-1β信号传导的复杂性。虽然,通常情况下,IL-6被标记为促炎,但它也可以作为抗炎介质。另一方面,IL-1β是主要的促炎因子,特别是在代谢紊乱中。这些细胞因子与巨噬细胞之间的关系是通过JAK/STAT和NFκB等重要通路介导的,这些通路被代谢应激干扰。因此,代谢应激也改变了巨噬细胞的功能参数,包括线粒体代谢、糖酵解和氧化代谢的改变。磷酸化改变了涉及能量消耗的动力学,影响了它们的极化和功能。然而,有研究表明,IL-6和IL-1β在诱导M2极化时可能协同或竞争,重要的是,它们参与细胞因子释放、吞噬活性和组织修复过程。本文综述了近年来有关IL-6和IL-1β细胞因子参与巨噬细胞极化以及代谢应激如何改变细胞因子功能和协同关系的研究进展。更好地了解这些细胞因子将成为探索针对代谢紊乱的替代抗病毒策略的重要一步,从而批准进一步的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring the mechanism and crosstalk between IL-6 and IL- 1β on M2 macrophages under metabolic stress conditions

Exploring the mechanism and crosstalk between IL-6 and IL- 1β on M2 macrophages under metabolic stress conditions
Macrophages are highly variable immune cells that are important in controlling inflammation and maintaining tissue balance. The ability to polarize into two major types—M1, promoting inflammation, and M2, resolving inflammation and contributing to tissue repair—determines their specific roles in health and disease. M2 macrophages are particularly important for reducing inflammation and promoting tissue regeneration, but their function is shaped mainly by surrounding cells. This is evident in obesity, diabetes, and chronic inflammation. Although many cytokines regulate macrophage polarization, interleukin-6 (IL-6) and interleukin-1β (IL-1β) are major players, but their effects on M2 macrophage behavior under metabolic stress remain unclear. This study describes the intricacies within M2 macrophages concerning IL-6 and IL-1β signaling when under metabolic stress. Though, more frequently than not, IL-6 is labelled as pro-inflammatory, it can also behave as an anti-inflammatory mediator. On the other hand, IL-1β is the main pro-inflammatory agent, particularly in metabolic disorders. The relationship between these cytokines and the macrophages is mediated through important pathways such as JAK/STAT and NFκB, which get perturbed by metabolic stress. Therefore, metabolic stress also alters the functional parameters of macrophages, including alterations in mitochondrial metabolism, glycolytic and oxidative metabolism. Phosphorylation alters the kinetics involved in energy consumption and affects their polarization and their function. However, it has been suggested that IL-6 and IL-1β may work in concert or competition when inducing M2 polarization and, importantly, implicate cytokine release, phagocytic activity, and tissue repair processes. In this review, we discuss the recent literature on the participation of IL-6 and IL-1β cytokines in macrophage polarization and how metabolic stress changes cytokine functions and synergistic relations. A better understanding of these cytokines would serve as an important step toward exploring alternative antiviral strategies directed against metabolic disturbance and, hence, approve further endeavors.
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来源期刊
Cytokine
Cytokine 医学-免疫学
CiteScore
7.60
自引率
2.60%
发文量
262
审稿时长
48 days
期刊介绍: The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. * Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors. We will publish 3 major types of manuscripts: 1) Original manuscripts describing research results. 2) Basic and clinical reviews describing cytokine actions and regulation. 3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.
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