Mechanotransduction in Acute Lung Injury
Mechanotransduction in Acute Lung Injury
批准号:
7677746
负责人:
CHRISTOPHER M WATERS
金额:
$52.8万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-03 至 2013-03-31
关键词:
AGTR2 geneAcidsAcute Lung InjuryAdhesionsAdult Respiratory Distress SyndromeAlveolarAlveolusAtomic Force MicroscopyBiologicalBlood capillariesCell AdhesionCell Adhesion InhibitionCell Migration Inhibition functionCellsClinical ResearchConfocal MicroscopyDiagnostic radiologic examinationDiseaseEndotheliumEpithelialEpithelial CellsEpitheliumExhibitsFigs - dietaryFocal Adhesion Kinase 1GasesHeterogeneityImageImageryIn VitroIncidenceInfectionInjuryIntensive Care UnitsLeadLifeLungMechanical ventilationMechanicsOutcomeOxygenPathogenesisPathway interactionsPatientsPhosphorylationPredispositionProcessPropertyPulmonary EdemaRattusResearchRoentgen RaysSignal TransductionStretchingTestingTherapeutic InterventionVentilator-induced lung injuryatelectraumacapillarycell motilityeconomic impactimprovedin vitro Modelin vivoinjuredinsightlung injurymigrationmortalitypressurepublic health relevancerepairedrestorationsurfactantwound
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Acute lung injury and its more severe form, acute respiratory distress syndrome (ARDS), are devastating illnesses with high rates of incidence and high mortality rates. Patients with acute lung injury are typically provided supplemental oxygen using positive pressure mechanical ventilation, but this can lead to additional injury, termed ventilator induced lung injury (VILI). The long term objective of this proposal is to improve understanding of the mechanisms by which overdistention (or stretch) of pulmonary epithelial cells contributes to ventilator-induced lung injury. The central hypothesis is that overdistention contributes both to the initiation of epithelial injury through loss of cell adhesion and to inhibition of repair mechanisms through decreased cell migration. Mechanisms of the initiation of VILI will be investigated using rats exposed to acid injury or surfactant depletion and direct visualization of airspace mechanics by microfocal Xray imaging. A combination of in vitro, in vivo, and ex vivo approaches will be used to investigate the hypothesis that mechanical stretch causes loss of cell adhesion and inhibition of repair mechanisms through focal adhesion kinase (FAK) signaling. These approaches include primary cultures of rat alveolar type II (AT2) epithelial cells isolated from rats following mechanical ventilation, exposure of cells to mechanical stretch in vitro, and confocal microscopy of isolated rat lungs. Finally, atomic force microscopy will be used to test the hypothesis that localized changes in mechanical stiffness regulate the repair mechanisms of AT2 cells in culture. The proposed studies will investigate the mechanisms that contribute to lung injury during mechanical ventilation and provide new insights into mechanotransduction, the process of converting mechanical signals to biological signals. PUBLIC HEALTH RELEVANCE: Acute lung injury is a devastating illness that results in significant loss of life and substantial economic impact due to extended stays in the intensive care unit. The proposed studies will investigate the mechanisms that contribute to lung injury during mechanical ventilation and will identify potential targets for therapeutic intervention.
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