Thiol Isomerases During Thrombus Formation

血栓形成过程中的硫醇异构酶

• 批准号: 8267644
• 负责人: BARBARA C FURIE
• 金额: $ 43.14万
• 依托单位: BETH ISRAEL DEACONESS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-01 至 2014-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8267644
• 关键词: Alpha Granule; Animal Model; Antibodies; Appearance; Binding; Biochemical; Blood Platelets; Cell membrane; Cell surface; Characteristics; Collagen; Confocal Microscopy; Disease; Electron Microscopy; Electron Transport; Endoplasmic Reticulum; Endothelial Cells; Enzymes; Equilibrium; Extracellular Protein; Family; Fibrin; Flow Cytometry; Generations; Health; Hemostatic Agents; Hemostatic function; Immunofluorescence Microscopy; In Vitro; Injury; Integrins; Intervention; Isomerase; Kinetics; Knowledge; Label; Laser injury; Lasers; Life; Literature; Mass Spectrum Analysis; Membrane; Membrane Proteins; Modeling; Monitor; Morbidity - disease rate; Mus; Organelles; Oxidation-Reduction; P-Selectin; Platelet Activation; Play; Process; Property; Protein Biosynthesis; Protein Disulfide Isomerase; Proteins; Regulation; Reporting; Research; Research Design; Research Methodology; Rest; Role; Scheme; Site; Stroke; Sulfhydryl Compounds; Surface; Testing; Therapeutic Embolization; Thrombin; Thromboplastin; Thrombosis; Thrombus; Two-Dimensional Gel Electrophoresis; United States; VWF gene; atherothrombosis; design; disulfide bond; endoplasmic reticulum glycoprotein p72; extracellular; ferric chloride; in vivo; member; mortality; novel; oxidation; protein function; release of sequestered calcium ion into cytoplasm; research study; tool

DESCRIPTION (provided by applicant): Thiol isomerases are critical for disulfide bond formation during protein synthesis within the endoplasmic reticulum, but protein thiol isomerases located outside of the endoplasmic reticulum may be critical for regulation of redox-sensitive allosteric disulfide bonds in proteins. Thiol isomerases in platelets and endothelial cells may play an important role in the regulation of protein function during thrombus formation. Our hypothesis is that each thiol isomerase that putatively influences thrombus formation in vivo has a specific function on a specific substrate(s). Protein disulfide isomerase and members of the PDI family will be identified in resting platelets and unstimulated endothelial cells, and localized to either the cell surface or internal organelles, or both, by flow cytometry, immunofluorescence microscopy and electron microscopy. The redistribution of thiol isomerases during platelet activation and endothelial cell stimulation, with special focus on the release of the enzymes and their binding to the cell surface, will be explored. To identify potential thiol isomerase substrates, proteins expressing free thiols on the surface of platelets and endothelial cells will be labeled, the membranes purified, and these proteins separated by 2D gel electrophoresis using 16-BAC/SDS. These labeled membrane proteins will be identified by mass spectrometry and will represent possible thiol isomerase substrates. To determine the role of thiol isomerases during thrombus formation, the kinetics of expression of thiol isomerases, including PDI, ERp5, ERp54, ERp72, ERp46, ERdj5, TMX and TMX3 will be studied in a live mouse by intravital multichannel widefield and confocal microscopy. The effect on inhibition of each thiol isomerase using antibodies specific for thiol isomerases on platelet activation monitored by calcium mobilization, platelet alpha granule release detected by P-selectin expression, fibrin formation, thrombin activity, platelet accumulation, platelet on/off rates, platelet thrombus embolization, microparticle accumulation, vWF accumulation, TF expression, and collagen exposure will be evaluated in the laser-induced vessel wall injury model and the ferric chloride model in a living mouse. These studies are designed to determine the role of thiol isomerases released from platelets and endothelial cells, and their contribution to the modulation of function of proteins involved in thrombosis and hemostasis, including but not limited to GPIb, GPIIbIIIa and tissue factor. PUBLIC HEALTH RELEVANCE: Evidence is mounting that important steps in the process of thrombus formation are regulated by the oxidation states of labile disulfide bonds in critical hemostatic proteins. The oxidation state of these bonds is regulated by an enzyme(s) of the thiol isomerase family. The central hypothesis of the proposed research is that specific thiol isomerases act on specific substrates critical to thrombus formation and thus regulate the thrombotic balance. The experiments described in the Research Design and Methods section of this proposal are designed to test this hypothesis. Establishment of a role for thiol isomerases in regulation of thrombus formation could provide novel targets for intervention in thrombotic disorders, atherothrombosis, stroke and thromboembolic disease, major causes of morbidity and mortality in the United States.

描述（由申请人提供）：硫醇异构酶在内质网内蛋白质合成过程中对于二硫键形成至关重要，但位于内质网外部的蛋白质硫醇异构酶可能对于蛋白质中氧化还原敏感的变构二硫键的调节至关重要。血小板和内皮细胞中的硫醇异构酶可能在血栓形成过程中的蛋白质功能调节中发挥重要作用。我们的假设是，假定影响体内血栓形成的每种硫醇异构酶对特定底物具有特定功能。通过流式细胞术、免疫荧光显微镜和电子显微镜，可以在静息血小板和未刺激的内皮细胞中鉴定蛋白质二硫键异构酶和 PDI 家族成员，并定位于细胞表面或内部细胞器，或两者。将探讨血小板活化和内皮细胞刺激期间硫醇异构酶的重新分布，特别关注酶的释放及其与细胞表面的结合。为了鉴定潜在的硫醇异构酶底物，将标记血小板和内皮细胞表面表达游离硫醇的蛋白质，纯化膜，并使用 16-BAC/SDS 通过 2D 凝胶电泳分离这些蛋白质。这些标记的膜蛋白将通过质谱法进行鉴定，并代表可能的硫醇异构酶底物。为了确定硫醇异构酶在血栓形成过程中的作用，将通过活体多通道宽场和共聚焦显微镜在活体小鼠中研究硫醇异构酶（包括 PDI、ERp5、ERp54、ERp72、ERp46、ERdj5、TMX 和 TMX3）的表达动力学。使用硫醇异构酶特异性抗体抑制每种硫醇异构酶对通过钙动员监测的血小板活化、通过P-选择素表达检测的血小板α颗粒释放、纤维蛋白形成、凝血酶活性、血小板积累、血小板开/关率、血小板血栓栓塞、微粒积累、vWF积累、TF表达和胶原暴露的影响将是 在活体小鼠的激光诱导血管壁损伤模型和氯化铁模型中进行了评估。这些研究旨在确定血小板和内皮细胞释放的硫醇异构酶的作用，及其对血栓形成和止血相关蛋白质功能调节的贡献，包括但不限于 GPIb、GPIIbIIIa 和组织因子。公共健康相关性：越来越多的证据表明，血栓形成过程中的重要步骤受到关键止血蛋白中不稳定二硫键氧化态的调节。这些键的氧化态由硫醇异构酶家族的酶调节。该研究的中心假设是，特定的硫醇异构酶作用于对血栓形成至关重要的特定底物，从而调节血栓平衡。本提案的研究设计和方法部分中描述的实验旨在检验这一假设。硫醇异构酶在血栓形成调节中的作用的确立可以为干预血栓性疾病、动脉粥样硬化血栓形成、中风和血栓栓塞性疾病（美国发病率和死亡率的主要原因）提供新的靶点。