昼夜代谢调节巨噬细胞的炎症反应

Yulong Sun, Wenjiao Jiang, T. Horng
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引用次数: 0

摘要

巨噬细胞是先天免疫系统的重要组成部分,协调宿主对微生物感染的防御,并塑造组织损伤后的重塑反应。代谢现在被认为是巨噬细胞身份和功能的强大而普遍的调节器。暴露于微生物配体后,巨噬细胞的炎症激活及其诱导的吞噬、炎症反应和其他宿主防御活动是由细胞代谢的动态变化支持的。值得注意的是,代谢活动以昼夜节律的方式受到强有力的调节,许多代谢过程在昼夜节律周期的一个阶段显示峰值活性,而在反阶段显示低谷活性。在这里,我们回顾了最近的研究结果,表明昼夜代谢影响巨噬细胞活动,特别是炎症反应。首先,我们总结了巨噬细胞活动已知显示的时间依赖性变化及其机制基础。其次,我们回顾了巨噬细胞中已被证明有节律调节的代谢过程,并讨论了这种昼夜节律代谢如何影响或可能影响巨噬细胞的活动。第三,我们讨论了巨噬细胞时钟携带的概念,并考虑巨噬细胞活动节律调节的丧失如何导致轮班工作、肥胖和衰老等病理生理状况。最后,我们提出昼夜节律代谢可以用来理解感染期间炎症反应动态调节的基本原理和机制基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circadian metabolism regulates the macrophage inflammatory response
Macrophages are an integral part of the innate immune system and coordinate host defense to microbial infections, as well as shaping the remodeling response after tissue injury. Metabolism is now appreciated to be a powerful and pervasive regulator of the identity and function of macrophages. Upon exposure to microbial ligands, macrophage inflammatory activation and the associated induction of phagocytosis, inflammatory responses and other host defense activities are supported by dynamic changes to cellular metabolism. Of note, metabolic activity is robustly regulated in a circadian fashion, with many metabolic processes displaying peak activity in one phase of the circadian cycle and trough activity in an antiphase manner. Here, we review recent findings that suggest that circadian metabolism influences macrophage activities and particularly the inflammatory response. First, we summarize macrophage activities known to display time-of-day dependent variation and their mechanistic basis. Second, we review metabolic processes that have been shown to be rhythmically regulated in macrophages and discuss how such circadian metabolism affects or is likely to affect macrophage activities. Third, we discuss the concept of entrainment of the macrophage clock, and consider how loss of rhythmic regulation of macrophage activities may contribute to pathophysiological conditions like shift work, obesity and aging. Finally, we propose that circadian metabolism can be used to understand the rationale and mechanistic basis of dynamic regulation of inflammatory responses during infection.
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