CXC Chemokines and Regulation of Granulopoiesis

CXC趋化因子和粒细胞生成的调节

• 批准号: 8439395
• 负责人: George SCOTT WORTHEN
• 金额: $ 39.36万
• 依托单位: CHILDREN'S HOSP OF PHILADELPHIA
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-03-15 至 2018-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8439395
• 关键词: Ablation; Address; Apoptotic; Attenuated; Bacteria; Bacterial Infections; Bacterial Pneumonia; CSF3 gene; CXC Chemokines; CXCL5 gene; Cells; Data; Environment; Epithelial Cells; Feedback; Gene Expression; Genes; Granulopoiesis; Host Defense; Host resistance; Hyperplasia; IL8RB gene; Inflammation; Inflammatory; Interleukin-1; Interleukin-17; Intestines; Ligands; Lung; Lung diseases; Lymphocyte; Lymphoid; Lymphoid Cell; Marrow; Mediating; Microbe; Modeling; Modification; Mus; Organ; Pathway interactions; Phagocytes; Phagocytosis; Phenotype; Pneumonia; Process; Production; Recruitment Activity; Regulation; Resistance; Role; Route; Sentinel; Severities; Signal Transduction; Site; Source; Stimulus; Surface; System; Testing; Tissues; antimicrobial; bacterial resistance; base; chemokine receptor; commensal microbes; improved; interleukin-23; macrophage; microbiome; mucosal site; neutrophil; novel strategies; pathogen; progenitor; public health relevance; receptor; response; trafficking

DESCRIPTION (provided by applicant): The chemokine receptor CXCR2 is the only receptor for ELR+ CXC chemokines in the mouse, deletion of which increases of neutrophils and progenitors in the marrow, as well as systemic expression of G-CSF and IL-17A. Our CXCL5-/- mice, which lack one ligand for CXCR2, express an intermediate phenotype, suggesting involvement of CXCL5 in controlling granulopoiesis through CXCR2. Furthermore, these mice are more resistant to severe pneumonia. Our data suggest that IL-17 regulates this phenotype in response to signals from the environment. Based on new preliminary data indicating that ablation of commensal bacteria impairs lung host defense, we hypothesize that commensal bacteria induce IL-17-expressing lymphoid cells in the gut that is attenuated by CXCL5- induced influx of neutrophils. In the absence of full neutrophil availability, IL-17- producing cells initite a systemic process inducing granulopoiesis and increasing lung host defense. Using murine systems, we will address the following Specific Aims: 1. Determine whether granulocytic hyperplasia in CXCR2-/- and CXCL5-/- mice is due to activation of an IL-1/IL-23/IL-17/G-CSF pathway, addressing whether the source of IL-17 is at mucosal sites, and the role of innate lymphoid cells. 2. Determine whether the IL- 17/G-CSF axis mediates the enhanced lung host defense seen in CXCL5-/- mice, focusing on regulation of trafficking of IL-17 cells and neutrophils, and modification of lung host defense genes 3. Determine the importance of commensal bacteria in regulating host defense through IL-17. These studies will address critical unanswered questions in how alterations in gut microbes may alter the lung resistance to bacterial infection, and offer new routes to enhance host resistance or decrease neutrophilic inflammation in the lung.

描述（由申请人提供）：趋化因子受体CXCR2是小鼠ELR+ CXC趋化因子的唯一受体，其缺失会增加骨髓中的中性粒细胞和祖细胞，以及G-CSF和IL-17A的全身表达。我们的CXCL5-/-小鼠缺乏一种CXCR2配体，表达一种中间表型，表明CXCL5通过CXCR2参与控制颗粒生成。此外，这些小鼠对严重肺炎的抵抗力更强。我们的数据表明，IL-17通过响应来自环境的信号来调节这种表型。基于新的初步数据表明，共生菌的消融会损害肺宿主防御，我们假设共生菌诱导肠道中表达il -17的淋巴细胞被CXCL5诱导的中性粒细胞内流减弱。在中性粒细胞缺乏的情况下，产生IL-17的细胞启动一个系统性过程，诱导粒细胞生成并增加肺宿主防御。使用小鼠系统，我们将解决以下具体目标：1。确定CXCR2-/-和CXCL5-/-小鼠的粒细胞增生是否由于IL-1/IL-23/IL-17/G-CSF通路的激活，确定IL-17的来源是否在粘膜部位，以及先天淋巴样细胞的作用。2. 确定IL-17 /G-CSF轴是否介导CXCL5-/-小鼠肺宿主防御增强，重点关注IL-17细胞和中性粒细胞运输的调节，以及肺宿主防御基因的修饰3。确定共生菌通过IL-17调节宿主防御的重要性。这些研究将解决肠道微生物改变如何改变肺部对细菌感染的抵抗力的关键问题，并提供增强宿主抵抗力或减少肺部中性粒细胞炎症的新途径。