Lymphoid Tissue Microvessel Growth
Lymphoid Tissue Microvessel Growth
批准号:
7725828
负责人:
Theresa T. Lu
金额:
$38.24万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-11-15 至 2011-10-31
关键词:
AffectAngiogenesis InhibitorsAngiolymphoid hyperplasiaAntineoplastic AgentsAutoimmune DiseasesAutoimmune ProcessBiological AssayBiological ModelsBloodBlood VesselsBone MarrowCell MaturationCell ProliferationCell physiologyCell surfaceCellsChimera organismCoculture TechniquesDataDendritic CellsDevelopmentDiseaseDrug Delivery SystemsEndothelial CellsEnzyme-Linked Immunosorbent AssayFibroblastsFunctional disorderGeneticGenetic ModelsGoalsGrowthITGAM geneITGAX geneImmuneImmune System DiseasesImmune responseImmune systemImmunizationL-SelectinLeadLeukocytesLightLymphatic DiseasesLymphocyteLymphoid TissueLymphomaLymphoproliferative DisordersMalignant - descriptorMediatingMediator of activation proteinMicronutrientsMolecularMusNutrientPathologicPeripheralPharmaceutical PreparationsPhysiologicalPopulationProcessRecruitment ActivityRegulationReporterResearch PersonnelRoleSourceStimulusStromal CellsSyndromeSystemic Lupus ErythematosusT-LymphocyteTechniquesTestingTherapeutic AgentsTissuesTumor AngiogenesisTumor Necrosis Factor-BetaUrsidae FamilyVascular Endothelial Growth FactorsVascular blood supplyWorkangiogenesiscadherin 5cancer cellcell growthcell typeimmune functionin vitro Assayinnovationinsightlymph nodeslymphotoxin beta receptormigrationmonocytemouse modelnovelnovel therapeuticsovarian neoplasmprogramstraffickingtumor
中文摘要
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英文摘要
Lymph nodes grow rapidly and robustly at the inititation of an immune response and this growth is
accompanied by growth of its blood vessels. The blood vessels are critical for supplying nutrients and for
regulating cell trafficking into the lymph node. Recent studies have begun to delineate the mechanisms that
regulate vascular growth in tumors and in a number of other processes, and these studies have led to
development of drugs that target vascular growth. In contrast, the regulation of vascular growth in the lymph
node during immune responses and the potential utility of anti-angiogenic therapies as immune modulators
are not well understood. This application proposes to investigate the regulation of lymph node vascular
growth by testing the hypothesis that, at the initiation of an immune response, mature dendritic cells prepare
the the lymph node microenvironment for the forthcoming expansion by inducing vascular growth. We will
test this hypothesis via these aims: 1) Determine the extent to which stimulated dendritic cells influences the
induction of endothelial proliferation by using mice with migration-defective dendritic cells, assessing the
requirement for dendritic cells on lymph node VEGF levels, and assessing the angiogenic potential of mature
and immature dendritic cells in in-vitro assays. 2) Establish the identity, regulation, and importance of
VEGF-expressing cells and establish the importance of vascular growth to immune function by using VEGF-
reporter mice, investigating regulation by lymphotoxin, and investigating lymphocyte trafficking with vascular
growth blockade. 3) Delineate the lineage and role of a novel cell type that bears both dendritic and
endothelial markers by dendritic cell depletion, inhibiting monocyte recruitment in CCR2-/- mice, fate tracing
of likely bone marrow precursors and testing the sufficiency of these cells. These studies will yield novel
information about dendritic cell functions and about the control of lymph node vascular growth and may have
implications for understanding and treatment of Castleman's disease, systemic lupus erythematosus, and
other lymphoproliferative and autoimmune diseases that affect lymph node and lymph node vascular growth.
Controlling lymph node blood vessel growth can potentially help to control growth of autoimmune or
cancer cells in the lymph node. These studies will investigate the mechanisms that regulate lymph node
vessel growth and may lead to the development of new therapies for lymphomas and immune diseases.
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会议论文
Diversity supplement: Lymphatic regulation of lymph node function in lupus
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批准号:10794867
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项目类别:
-
资助金额:$7.04万
-
财政年份:2023
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负责人:Theresa T. Lu
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依托单位:
Skin-lymph node axis in SLE
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批准号:10666573
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项目类别:
-
资助金额:$19.34万
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财政年份:2022
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负责人:Theresa T. Lu
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依托单位:
Skin-lymph node axis in SLE
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批准号:10510072
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项目类别:
-
资助金额:$25.26万
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财政年份:2022
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负责人:Theresa T. Lu
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依托单位:
Vascular Quiescence and Stabilization in Immunity
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批准号:8213586
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项目类别:
-
资助金额:$43.44万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular Quiescence and Stabilization in Immunity
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批准号:8013874
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项目类别:
-
资助金额:$43.44万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular Quiescence and Stabilization in Immunity
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批准号:7887391
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项目类别:
-
资助金额:$43.76万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular-stromal function and regulation in immunity
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批准号:10312108
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项目类别:
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资助金额:$44.0万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular Quiescence and Stabilization in Immunity
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批准号:8604356
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项目类别:
-
资助金额:$43.44万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular-stromal function and regulation in immunity
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批准号:10062843
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项目类别:
-
资助金额:$44.0万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Lymphatic regulation of lymph node function in lupus
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批准号:10587191
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项目类别:
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资助金额:$55.6万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Vascular Quiescence and Stabilization in Immunity
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批准号:8416444
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项目类别:
-
资助金额:$40.83万
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财政年份:2010
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负责人:Theresa T. Lu
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依托单位:
Lymphoid Tissue Microvessel Growth
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批准号:7531814
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项目类别:
-
资助金额:$38.63万
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财政年份:2006
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负责人:Theresa T. Lu
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依托单位:
Lymphoid Tissue Microvessel Growth
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批准号:7993536
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项目类别:
-
资助金额:$37.86万
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财政年份:2006
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负责人:Theresa T. Lu
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依托单位:
Lymphoid Tissue Microvessel Growth
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批准号:7198508
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项目类别:
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资助金额:$39.12万
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财政年份:2006
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负责人:Theresa T. Lu
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依托单位:
Lymphoid Tissue Microvessel Growth
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批准号:7314651
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项目类别:
-
资助金额:$38.59万
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财政年份:2006
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负责人:Theresa T. Lu
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依托单位:
海外基金