Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Department of Immunology and Oncode Institute, Leiden University Medical Center, Leiden, Netherlands.
Front Immunol. 2021 Mar 19;12:621665. doi: 10.3389/fimmu.2021.621665. eCollection 2021.
Toll-like receptor 5 (TLR5) is the receptor of bacterial Flagellin. Reportedly, TLR5 engagement helps to combat infections, especially at mucosal sites, by evoking responses from epithelial cells and immune cells. Here we report that TLR5 is expressed on a previously defined bipotent progenitor of macrophages (MΦs) and osteoclasts (OCs) that resides in the mouse bone marrow (BM) and circulates at low frequency in the blood. , Flagellin promoted the generation of MΦs, but not OCs from this progenitor. , MΦ/OC progenitors were recruited from the blood into the lung upon intranasal inoculation of Flagellin, where they rapidly differentiated into MΦs. Recruitment of the MΦ/OC progenitors into the lung was likely promoted by the CCL2/CCR2 axis, since the progenitors expressed CCR2 and type 2 alveolar epithelial cells (AECs) produced CCL2 upon stimulation by Flagellin. Moreover, CCR2 blockade reduced migration of the MΦ/OC progenitors toward lung lavage fluid (LLF) from Flagellin-inoculated mice. Our study points to a novel role of the Flagellin/TLR5 axis in recruiting circulating MΦ/OC progenitors into infected tissue and stimulating these progenitors to locally differentiate into MΦs. The progenitor pathway to produce MΦs may act, next to monocyte recruitment, to fortify host protection against bacterial infection at mucosal sites.
Toll 样受体 5(TLR5)是细菌鞭毛蛋白的受体。据报道,TLR5 的激活有助于通过上皮细胞和免疫细胞的反应来对抗感染,特别是在黏膜部位。在这里,我们报告 TLR5 表达在一个以前定义的巨噬细胞(MΦ)和破骨细胞(OC)的双潜能祖细胞上,该祖细胞存在于小鼠骨髓(BM)中,并在血液中以低频率循环。Flagellin 促进了这种祖细胞向 MΦ的生成,但不能向 OC 生成。在 Flagellin 鼻内接种后,MΦ/OC 祖细胞从血液中招募到肺部,在那里它们迅速分化为 MΦ。MΦ/OC 祖细胞向肺部的招募可能是由 CCL2/CCR2 轴促进的,因为祖细胞表达 CCR2,并且在受到 Flagellin 刺激时 II 型肺泡上皮细胞(AEC)产生 CCL2。此外,CCR2 阻断减少了 MΦ/OC 祖细胞向来自 Flagellin 接种小鼠的肺灌洗液(LLF)的迁移。我们的研究指出了 Flagellin/TLR5 轴在招募循环 MΦ/OC 祖细胞进入感染组织并刺激这些祖细胞在局部分化为 MΦ方面的新作用。产生 MΦ的祖细胞途径可能与单核细胞募集一起,增强宿主对黏膜部位细菌感染的保护作用。