Macrophages in metaflammation - fueling chronic inflammation in metabolic disease.

IF 3.2 4区 医学 Q2 PHYSIOLOGY
Ronja Kardinal, Dagmar Wachten
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引用次数: 0

Abstract

Obesity is a leading global health issue, closely associated with a chronic low-grade inflammation termed metaflammation. Metaflammation is driven by immune cell reprogramming, particularly of macrophages. In white adipose tissue (WAT), obesity induces a shift from anti-inflammatory to pro-inflammatory macrophage phenotypes, contributing to insulin resistance and tissue fibrosis. Recent studies have also illuminated the role of macrophages in brown and beige adipose tissue (BAT and scWAT), where they influence thermogenic capacity. Beyond the adipose tissue, the liver is the other main metabolic organ impacted by obesity. Liver macrophages play a critical role in the pathogenesis of metabolic dysfunction-associated steatotic liver disease (MASLD) by promoting inflammation, lipid accumulation, and fibrosis. This review highlights the role of macrophages in the development and regulation of metaflammation in metabolic organs.

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巨噬细胞在代谢性疾病中发生性炎症中的作用。
肥胖是一个主要的全球健康问题,与慢性低度炎症密切相关,称为炎症。继发炎症是由免疫细胞重编程,特别是巨噬细胞的重编程驱动的。在白色脂肪组织(WAT)中,肥胖诱导巨噬细胞表型从抗炎向促炎转变,导致胰岛素抵抗和组织纤维化。最近的研究也阐明了巨噬细胞在棕色和米色脂肪组织(BAT和scWAT)中的作用,在那里它们影响产热能力。除了脂肪组织,肝脏是另一个受肥胖影响的主要代谢器官。肝巨噬细胞通过促进炎症、脂质积累和纤维化,在代谢功能障碍相关脂肪变性肝病(MASLD)的发病机制中发挥关键作用。本文综述了巨噬细胞在代谢器官中发生性炎症的发展和调控中的作用。
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来源期刊
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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