LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
批准号:
7429961
负责人:
DALE A SCHUSCHKE
金额:
$0.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-08-01 至 2009-03-31
关键词:
AcuteAcute Lung InjuryAdhesionsAnimalsBloodBlood VesselsCell AdhesionCell Adhesion MoleculesCell CommunicationCellsChemotaxisConditionCopperDevelopmentDietDietary CopperEndothelial CellsEndotheliumExtravasationGoalsHemostatic functionImmunologicsInflammationInflammatoryInflammatory ResponseIntakeIntercellular adhesion molecule 1LeukocytesLungMediatingMicrocirculationNF-kappa BNFKB Signaling PathwayNitric OxideProcessRattusReactionRegulationResearchRoleStimulusThrombosisTissuesVascular Endothelial CellVasodilationWorkadhesion processbasedaydietary requirementhypocupremiain vitro Modelin vivoneutrophilpreventresearch studyresponse
中文摘要
微血管对炎症刺激反应的调节高度依赖于
英文摘要
Regulation of the microvascular response to inflammatory stimuli is highly dependent upon the
interactions between neutrophils and the endothelium. We have shown a significant role for dietary
copper in various endothelial interactions in the inflammatory process, including nitric oxide
(NO)-mediated vasodilation, macromolecular leakage, and thrombosis. Recently, we have studied the
role of dietary copper in microvascular control mechanisms with an emphasis on leukocyte/endothelial
adhesion. We have demonstrated that dietary copper restriction causes tissue-specific changes in
neutrophil/endothelial adhesion and transmigration. Neutrophil accumulation, the expression of the
adhesion molecule ICAM-1 and the transcription factor NF-kB are all greater in the lungs of
copper-deficient rats compared to copper-adequate controls. Based on these results, we hypothesize that
dietary copper deficiency has a priming effect on leukocytes and pulmonary vascular endothelial ceils
such that the lung becomes hypersensitive to inflammatory stimuli and more susceptible to the
development of acute lung injury. Therefore the specific aims of this study are to: 1) determine the role of
dietary copper in leukocyte/endothelial cell interactions in the lung microcirculation; 2) determine the
mechanisms by which copper deficiency primes cells for acute inflammation and 3) determine at what
concentration of dietary copper the inflammatory mechanisms become enhanced in the in vivo animal
microcirculation. Aim #1 will use both in vivo and in vitro models of the lung microcirculation to study
leukocyte/endothelial cell adhesion and chemotaxis. Aim #2 will study the role of copper in the NF-kB
signaling pathway and in neutrophil priming. Aim #3 will examine these mechanisms under conditions of
copper-marginal diets. These experiments have particular relevance since analysis of typical Western
diets suggest that 1/3 to 1/2 of those diets may provide less than the RDA of 900mg Cu/day.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:6864950
-
项目类别:
-
资助金额:$21.09万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:7285567
-
项目类别:
-
资助金额:$19.01万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:6381450
-
项目类别:
-
资助金额:$12.23万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:6177992
-
项目类别:
-
资助金额:$11.49万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:7390740
-
项目类别:
-
资助金额:$18.59万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:7046094
-
项目类别:
-
资助金额:$19.61万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:6523771
-
项目类别:
-
资助金额:$12.19万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
LEUKOCYTE ADHESION IN COPPER DEFICIENT MICROCIRCULATION
-
批准号:2908137
-
项目类别:
-
资助金额:$11.15万
-
财政年份:1999
-
负责人:DALE A SCHUSCHKE
-
依托单位:
海外基金