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Circadian gene Bmal1 regulates diurnal oscillations of Ly6Chi inflammatory monocytes

机译:昼夜节律基因Bmal1调节Ly6Chi炎性单核细胞的昼夜振荡

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摘要

Circadian clocks have evolved to regulate physiologic and behavioral rhythms in anticipation of changes in the environment. Although the molecular clock is present in innate immune cells, its role in monocyte homeostasis remains unknown. Here, we report that Ly6Chi inflammatory monocytes exhibit diurnal variation, which controls their trafficking to sites of inflammation. This cyclic pattern of trafficking confers protection against Listeria monocytogenes and is regulated by the repressive activity of the circadian gene BMAL1. Accordingly, myeloid cell-specific deletion of BMAL1 induces expression of monocyte-attracting chemokines and disrupts rhythmic cycling of Ly6Chi monocytes, predisposing mice to development of pathologies associated with acute and chronic inflammation. These findings have unveiled a critical role for BMAL1 in controlling the diurnal rhythms in Ly6Chi monocyte numbers.
机译:昼夜节律时钟已经演变为在预期环境变化时调节生理和行为节律。尽管分子钟存在于先天免疫细胞中,但其在单核细胞稳态中的作用仍然未知。在这里,我们报道Ly6C hi 炎性单核细胞表现出昼夜变化,从而控制了它们向炎症部位的运输。这种贩运的循环模式赋予针对单核细胞增生性李斯特菌的保护作用,并受昼夜节律基因BMAL1的抑制活性调节。因此,BMAL1的髓样细胞特异性缺失诱导了吸引单核细胞的趋化因子的表达,并破坏了Ly6C s 单核细胞的节律循环,使小鼠易于发生与急性和慢性炎症相关的病理。这些发现揭示了BMAL1在控制Ly6C hi 单核细胞数量的昼夜节律中的关键作用。

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