Dong Guangyu, Song Liang, Tian Chen, Wang Yu, Miao Fang, Zheng Jiabao, Lu Chanyi, Alsadun Sarah, Graves Dana T
Department of Periodontics, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Department of Stomatology, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, China.
Front Immunol. 2017 Sep 4;8:1088. doi: 10.3389/fimmu.2017.01088. eCollection 2017.
Neutrophils play an essential role in the innate immune response to microbial infection and are particularly important in clearing bacterial infection. We investigated the role of the transcription factor FOXO1 in the response of neutrophils to bacterial challenge with and . In these experiments, the effect of lineage-specific FOXO1 deletion in LyzM.CreFOXO1 mice was compared with matched littermate controls. FOXO1 deletion negatively affected several critical aspects of neutrophil function including mobilization of neutrophils from the bone marrow (BM) to the vasculature, recruitment of neutrophils to sites of bacterial inoculation, and clearance of bacteria. FOXO1 regulated neutrophil chemotaxis and bacterial killing. Moreover, bacteria-induced expression of CXCR2 and CD11b, which are essential for several aspects of neutrophil function, was dependent on FOXO1 and . Furthermore, FOXO1 directly interacted with the promoter regions of CXCR2 and CD11b. Bacteria-induced nuclear localization of FOXO1 was dependent upon toll-like receptor (TLR) 2 and/or TLR4 and was significantly reduced by inhibitors of reactive oxygen species (ROS and nitric oxide synthase) and deacetylases (Sirt1 and histone deacetylases). These studies show for the first time that FOXO1 activation by bacterial challenge is needed to mobilize neutrophils to transit from the BM to peripheral tissues in response to infection as well as for bacterial clearance . Moreover, FOXO1 regulates neutrophil function that facilitates chemotaxis, phagocytosis, and bacterial killing.
中性粒细胞在对微生物感染的固有免疫反应中发挥着重要作用,在清除细菌感染方面尤为重要。我们研究了转录因子FOXO1在中性粒细胞对细菌攻击反应中的作用。在这些实验中,将LyzM.CreFOXO1小鼠中谱系特异性FOXO1缺失的影响与匹配的同窝对照进行了比较。FOXO1缺失对中性粒细胞功能的几个关键方面产生了负面影响,包括中性粒细胞从骨髓(BM)向脉管系统的动员、中性粒细胞向细菌接种部位的募集以及细菌的清除。FOXO1调节中性粒细胞趋化性和细菌杀伤作用。此外,细菌诱导的CXCR2和CD11b表达(这对中性粒细胞功能的几个方面至关重要)依赖于FOXO1。此外,FOXO1直接与CXCR2和CD11b的启动子区域相互作用。细菌诱导的FOXO1核定位依赖于Toll样受体(TLR)2和/或TLR4,并被活性氧(ROS)和一氧化氮合酶抑制剂以及去乙酰化酶(Sirt1和组蛋白去乙酰化酶)显著降低。这些研究首次表明,细菌攻击激活FOXO1是使中性粒细胞响应感染从BM转运至外周组织以及进行细菌清除所必需的。此外,FOXO1调节中性粒细胞功能,促进趋化性、吞噬作用和细菌杀伤。