Endothelial Regulation of Leukocyte Transmigration

白细胞迁移的内皮调节

• 批准号: 7455990
• 负责人: FRANCIS W. LUSCINSKAS
• 金额: $ 40.67万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-08-01 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7455990
• 关键词: Actins; Acute; Address; Adherent Culture; Adhesions; Adhesives; Amino Acids; Arteries; Atherosclerosis; Binding; Biochemical; Biological Assay; Biomechanics; Blood Vessels; Blood flow; Buffers; CXCR4 gene; Cell model; Cells; Characteristics; Chemotactic Factors; Chronic; Condition; Cytoplasmic Protein; Cytoplasmic Tail; Cytoskeleton; Data; Defect; Disease; E-Selectin; Endothelial Cells; Endothelium; Environment; Exhibits; Failure; Fluorescence; Fluorescence Recovery After Photobleaching; Funding; Goals; Green Fluorescent Proteins; Human; Image; Immune; In Vitro; Inflammation; Inflammatory; Injury; Intercellular Junctions; Intercellular adhesion molecule 1; Leukocytes; Life; Link; Location; Measurement; Mediating; Memory; Mesentery; Modeling; Mononuclear Leukocytes; Mus; Mutagenesis; Mutation; Neutrophil Infiltration; Organ; P-selectin ligand protein; Pathway interactions; Permeability; Phenotype; Physiological; Play; Protein Binding; Protein Overexpression; Proteins; Range; Reaction; Regulation; Reporting; Research Personnel; Retinal Cone; Role; Route; Signal Pathway; Signal Transduction; Site; Spatial Behavior; System; T memory cell; T-Lymphocyte; T-Lymphocyte Subsets; Tail; Techniques; Testing; Therapeutic Intervention; Tissues; Transgenic Mice; Vascular Endothelium; Vascular Permeabilities; Vascular System; Venous; Wild Type Mouse; Work; cellular imaging; cremaster muscle; cytokine; design; fluorescence imaging; in vitro Assay; in vitro Model; in vivo; in vivo Model; intravital microscopy; monocyte; monolayer; mutant; neutrophil; novel; programs; shear stress; trafficking

DESCRIPTION (provided by applicant): The interaction of neutrophils and mononuclear leukocytes with endothelium plays a pivotal role in leukocyte recruitment in acute and chronic inflammation, immune reactions, vascular injury and atherosclerosis. In the previous funding period, four major accomplishments occurred. (1) We identified a novel E-selectin dependent adhesion pathway in T cells subsets. (2) We determined that t-bet T cells have a defect in trafficking in vivo and in vitro related to impaired PSGL-1 function and failure to express CXCR4. (3) We developed a live cell fluorescence assay to resolve the temporal and spatial behavior of LFA-1 and ICAM-1 during leukocyte transmigration. (4) We developed an in vitro assay for non-junctional neutrophil transmigration. This proposal builds on this scientific progress and will consist of three interrelated specific aims that will focus on the role of endothelial cell ICAM-1 tail in leukocyte transmigration. Our working hypothesis is that during leukocyte adhesion, LFA-1 binds ICAM-1, triggering its association with the cytoskeleton, and this step functions in "outside in" signaling to promote ICAM-1 clustering around transmigrating leukocytes. Specific Aim 1 will elucidate the role of ICAM-1 cytoplasmic tail in leukocyte transmigration using biochemical and biophysical techniques as well as a newly developed live cell fluorescence imaging system and vascular endothelium that support both junctional and non-junctional transmigration. Specific Aim 2 will test the role of the ICAM-1 tail in chemoattractant driven leukocyte transmigration in an in vivo model of inflammation. Confocal intravital fluorescence imaging will visualize the sites of leukocyte transmigration (junctional or non-junctional route) using fluorescent markers of cell-cell junctions, and in parallel, determine whether the route of transmigration adversely effects vascular permeability. Specific Aim 3 will study the role of the ICAM-1 tail in an arterial endothelial cell model of inflammation in vitro. Endothelial monolayers of an arterial or venous phenotype will be created in vitro by applying a pulsatile shear stress in an arterial or venous waveform using a recently described cone-plate apparatus. The adhesive interactions and sites of transmigration of blood monocytes and memory T cells with the above conditioned endothelium will be examined. The information gained from these studies will help delineate the ICAM-1 dependent mechanisms underlying leukocyte transmigration and may thus define new targets for therapeutic intervention in immune and inflammatory diseases.

描述（由申请方提供）：中性粒细胞和单核白细胞与内皮的相互作用在急性和慢性炎症、免疫反应、血管损伤和动脉粥样硬化中的白细胞募集中起着关键作用。在上一个供资期间，取得了四项主要成绩。(1)我们确定了一种新的E-选择素依赖的粘附途径的T细胞亚群。(2)我们确定t-bet T细胞在体内和体外运输中存在缺陷，这与PSGL-1功能受损和CXCR 4表达失败有关。(3)我们开发了一种活细胞荧光分析法来解析LFA-1和ICAM-1在白细胞迁移过程中的时间和空间行为。(4)我们开发了一种非交界性中性粒细胞迁移的体外试验。该建议建立在这一科学进展的基础上，将包括三个相互关联的具体目标，重点是内皮细胞ICAM-1尾在白细胞迁移中的作用。我们的工作假设是，在白细胞粘附过程中，LFA-1结合ICAM-1，触发其与细胞骨架的关联，并且这一步骤在“由外而内”信号传导中起作用，以促进ICAM-1聚集在迁移的白细胞周围。具体目标1将阐明ICAM-1细胞质尾白细胞迁移的作用，使用生物化学和生物物理技术，以及新开发的活细胞荧光成像系统和血管内皮细胞，支持连接和非连接的迁移。特异性目的2将在体内炎症模型中测试ICAM-1尾在化学引诱物驱动的白细胞迁移中的作用。共焦活体荧光成像将使用细胞-细胞连接的荧光标记物可视化白细胞迁移的位点（连接或非连接途径），并同时确定迁移途径是否对血管通透性产生不利影响。具体目标3将研究ICAM-1尾在体外动脉内皮细胞炎症模型中的作用。动脉或静脉表型的内皮单层将通过使用最近描述的锥板装置在动脉或静脉波形中施加脉动剪切应力而在体外产生。将检查血液单核细胞和记忆T细胞与上述条件内皮的粘附相互作用和迁移位点。从这些研究中获得的信息将有助于描述ICAM-1依赖性机制的基础白细胞迁移，并可能因此定义新的目标，在免疫和炎症性疾病的治疗干预。