Polymicrobial induction of epithelial inflammation

多种微生物诱导上皮炎症

• 批准号: 6955295
• 负责人: Adam Jonathan Ratner
• 金额: $ 11.71万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-06-15 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6955295
• 关键词: Haemophilus influenzae; Streptococcus infection; Streptococcus pneumoniae; bacteria infection mechanism; bacterial cytopathogenic effect; bacterial toxins; biological signal transduction; cell line; cell migration; cytokine; cytoplasmic receptors; enzyme linked immunosorbent assay; host organism interaction; human tissue; inflammation; microorganism immunology; mucosal immunity; neutrophil; peptidoglycan; pore forming protein; respiratory epithelium; respiratory infections

DESCRIPTION (provided by applicant): Epithelial cells act as the most proximal arm of the innate immune system by sensing bacterial products and recruiting neutrophils to mucosal surfaces. During colonization, these cells are concurrently exposed to a vast array of microbial products, and it is not well understood how these combinations may alter the responses of epithelial cells. Preliminary data presented here describe a novel system for the generation of inflammation in the setting of polymicrobial stimulation. Concurrent exposure to two important human respiratory pathogens, S. pneumoniae and H. influenzae, induces synergistic production of proinflammatory cytokines by epithelial cells. This effect occurs both in vitro and in vivo and is associated with neutrophil recruitment. This proposal is designed to characterize the mechanism of this response. The first specific aim will address the hypothesis that specific bacterial components from S. pneumoniae and H. influenzae are necessary and sufficient for synergistic induction of inflammation. The second specific aim addresses specific host molecular mechanisms involved in this pathway. These studies have the potential to further the current understanding of immune responses at colonized mucosal surfaces, with implications for both colonization and invasive disease. This application describes a program designed to provide Dr. Adam Ratner with the skills necessary to become an independent investigator in microbial pathogenesis. Dr. Ratner has completed fellowship training in pediatric infectious diseases and will be mentored by Dr. Jeffrey Weiser, an expert in the pathogenesis of respiratory diseases. The program includes didactic study in the areas of genetics, immunology, and bacterial pathogenesis. In addition, an in-depth laboratory experience will expose Dr. Ratner to a wide variety of techniques in the areas of cell biology, biochemistry, physiology, and molecular biology, thus providing a solid foundation for beginning an independent research career.

描述（由申请人提供）：上皮细胞通过感测细菌产物并募集中性粒细胞到粘膜表面，作为先天免疫系统的最近端组。在定殖过程中，这些细胞同时暴露于大量的微生物产物中，并且尚不清楚这些组合如何改变上皮细胞的反应。此处提供的初步数据描述了一种新型的系统，用于在多数型刺激的情况下产生炎症。同时暴露于两种重要的人呼吸道病原体，肺炎链球菌和h。H.h. the，可引起上皮细胞促炎细胞因子的协同产生。这种作用在体外和体内都会发生，并且与中性粒细胞募集有关。该建议旨在表征这种反应的机制。第一个具体目的将解决以下假设：肺炎链球菌和流感链球菌的特定细菌成分对于协同诱导炎症是必要的，足以满足。第二个特定目的解决了该途径中涉及的特定宿主分子机制。这些研究有可能进一步了解定植粘膜表面上免疫反应的理解，这对定殖和侵入性疾病都有影响。 该应用程序描述了一个计划，旨在为亚当·拉特纳（Adam Ratner）博士提供成为微生物发病机理中独立研究者所需的技能。 Ratner博士已完成小儿传染病的研究金培训，并将由呼吸道疾病发病机理专家Jeffrey Weiser博士进行指导。该程序包括在遗传学，免疫学和细菌发病机理领域的教学研究。此外，深入的实验室经验将使Ratner博士在细胞生物学，生物化学，生理学和分子生物学领域的各种技术中展现出各种技术，从而为开始独立研究职业提供了坚实的基础。