COMPARATIVE PROTEOMIC INVESTIGATION OF ARDS AND SYSTEMIC INFLAMMATORY INJURY

ARDS 和全身炎症损伤的比较蛋白质组学研究

• 批准号: 8363737
• 负责人: Jane Hirsch
• 金额: $ 0.15万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-06-01 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8363737
• 关键词: Adult Respiratory Distress Syndrome; Alveolar; Animal Model; Blood Proteins; Blood capillaries; Chromatography; Clinical; Disease; Disease Marker; Electrophoresis; Evaluation; Filtration; Funding; Grant; Immunoassay; Inflammatory; Injury; Intensive Care; Investigation; Label; Liquid substance; Mass Spectrum Analysis; Mechanical ventilation; Medicine; Morbidity - disease rate; National Center for Research Resources; Principal Investigator; Proteins; Proteome; Proteomics; Publishing; Reaction; Research; Research Infrastructure; Resources; Sampling; Sepsis; Source; Syndrome; Tidal Volume; Trauma; Type II Epithelial Receptor Cell; United States National Institutes of Health; capillary; comparative; cost; improved; liver ischemia; mortality

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. The acute respiratory distress syndrome (ARDS) is one of the most important causes for morbidity and mortality in intensive care medicine. It can be the sequel of numerous diseases like mechanical ventilation, sepsis and trauma. The syndrome is characterized by an inflammatory reaction that leads to a breakdown of the alveolar-capillary barrier, resulting in an influx of fluid and proteins from the blood into the alveolar space. The exact mechanism of the inflammatory reaction is still incompletely understood. Numerous clinical and experimental trials have been made in order to improve the understanding and evaluate possible treatment options of this disease state. METHODS: The proposed study focuses on the evaluation of alveloar type II cells from animal models of ARDS compared to control samples. After protein labeling for quantitative analysis, separation by chromatography, filtration and electrophoresis, LC-MS-MS mass spectrometry is used to analyze the proteome in both groups in order to identify protein markers of disease. Content changes are further evaluated by immunoassays. So far alterations after mechanical ventilation with different tidal volumes and liver ischemia have been evaluated and published

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