Abstract

The circadian rhythm is a biological system that creates daily variations of physiology and behavior with a 24-h cycle, which is precisely controlled by the molecular circadian clock. The circadian clock dominates temporal activity of physiological homeostasis at the molecular level, including endocrine secretion, metabolic, immune response, coupled with extrinsic environmental cues (e.g., light/dark cycles) and behavioral cues (e.g., sleep/wake cycles and feeding/fasting cycles). The other side of the clock is that the misaligned circadian rhythm contributes to the onset of a variety of diseases, such as cancer, metabolic diseases, and cardiovascular diseases, the acceleration of aging, and the development of systemic inflammation. The role played by macrophages is a key mediator between circadian disruption and systemic inflammation. At the molecular level, macrophage functions are under the direct control of the circadian clock, and thus the circadian misalignment remodels the phenotype of macrophages toward a ‘killer’ mode. Remarkably, the inflammatory macrophages induce systemic and chronic inflammation, leading to the development of inflammatory diseases and the dampened immune defensive machinery against infectious diseases such as COVID-19. Here, we discuss how the circadian clock regulates macrophage immune functions and provide the potential risk of misaligned circadian rhythms against inflammatory and infectious diseases.

Highlights

  • Acute lower respiratory tract infections (LRTIs) remain the most lethal communicable diseases by causing life-threatening pneumonia

  • We summarize the protective roles of alveolar macrophages on acute LRTIs via phagocytosis, proinflammatory responses, and efferocytosis

  • LPSstimulated pro-inflammatory responses are heightened in alveolar macrophages isolated from mice lacking REV-ERBa compared to wild-type mice (Pariollaud et al, 2018). These findings suggest that the core clock component brain and muscle ARNT-like 1 (BMAL1) exerts anti-inflammatory effects via REV-ERBa in both alveolar and peripheral monocyte-derived macrophages (Figure 3)

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Summary

Introduction

Acute lower respiratory tract infections (LRTIs) remain the most lethal communicable diseases by causing life-threatening pneumonia. The loss of appropriate light/dark cycles disrupts circadian biological functions, including irregular temporal oscillation of hormone secretion and gene expression, through the SCN clock. The robust circadian oscillation of circulatory glucocorticoid results in the circadian regulation of inflammatory cytokine and chemokine expression, which governs the cyclic activity of systemic inflammation and immune response.

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