MAPPING THE STIMULUS-SPECIFIC SIGNALING PATHWAYS IN PERIODONTITIS BY PROTEOMICS

通过蛋白质组学绘制牙周炎中刺激特异性信号通路

• 批准号: 7602017
• 负责人: Salomon Amar
• 金额: $ 2.37万
• 依托单位: BOSTON UNIVERSITY MEDICAL CAMPUS
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-03 至 2008-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7602017
• 关键词: Bone Resorption; Cell Wall; Computer Retrieval of Information on Scientific Projects Database; Connective Tissue; Data; Development; Disease; Fimbria of hippocampus; Funding; Gram-Negative Anaerobic Bacteria; Grant; Human; Immune response; Inflammatory; Institution; Life; Lipopolysaccharides; Localized; Manuscripts; Maps; Methodology; Parasites; Periodontitis; Pigments; Pilum; Play; Porphyromonas gingivalis; Production; Proteomics; Research; Research Personnel; Resources; Role; Signal Pathway; Signal Transduction Pathway; Source; Stimulus; Structure; Testing; United States National Institutes of Health; alveolar bone; appendage; base; cytokine; macrophage; monocyte; pathogen; peripheral blood; protein expression; research study

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Periodontitis is an inflammatory disease with host-parasite interactions which contribute to connective tissue destruction and alveolar bone resorption. Porphyromonas gingivalis (P.g.) a black-pigmented Gram-negative anaerobic bacterium, is a major pathogen in the development and progression of periodontitis. Cell wall and appendage structures, such as lipopolysaccharide (LPS) and fimbriae (Fim A), play important roles in the induction of innate immune responses, including cytokine production by localized and circulating monocyte/macrophage. Based on preliminary data, live P.g. stimulates unique pro-inflammatory signal transduction pathways in human peripheral blood monocytes (PBM) and THP-1 as opposed to purified bacterial components. In these experiments we test at the level of protein expression that unique signaling pathways are differentially induced by live P.g., LPS and Fim A. A manuscript describing the development and first application of our methodology is in press.

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