Ask1 a novel regulator of platelet function

Ask1 一种新型血小板功能调节剂

• 批准号: 9034654
• 负责人: ULHAS P NAIK
• 金额: $ 39万
• 依托单位: THOMAS JEFFERSON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-02-01 至 2018-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9034654
• 关键词: Ablation; Adoptive Transfer; Affect; Affinity; Agonist; Binding; Biochemical; Biological Assay; Blood Circulation; Blood Platelets; Blood Vessels; Bone Marrow Cells; Cardiovascular Diseases; Cause of Death; Cells; Clot retraction; Coagulation Process; Complex; Cytoplasmic Granules; Cytoskeleton; Data; Defect; Disease; Event; Family; Fibrinogen; Fibrinogen Receptors; Generations; Genetic; Health; Hemorrhage; Hemostatic function; Human; In Vitro; Injury; Integrins; Knock-in Mouse; Lead; Life; MAP Kinase Kinase Kinase; MAP3K5 gene; MAPK1 gene; MAPK14 gene; Membrane; Mitogen-Activated Protein Kinases; Modeling; Molecular; Mus; Myocardial Infarction; Participant; Pathogenesis; Phenotype; Physiological; Platelet Activating Factor; Platelet Activation; Platelet aggregation; Play; Process; Production; Proteins; Recruitment Activity; Regulation; Research; Role; Serotonin; Shapes; Signal Pathway; Signal Transduction; Signaling Molecule; Stress; Stroke; Structure-Activity Relationship; Techniques; Testing; Therapeutic Agents; Therapy Evaluation; Thrombin; Thrombosis; Thromboxane A2; Thrombus; VWF gene; Wound Healing; combat; genetic approach; in vivo; in vivo Model; mutant; novel; novel therapeutic intervention; receptor; therapeutic target

DESCRIPTION (provided by applicant): The foremost cause of death in humans is cardiovascular diseases such as myocardial infarction and stroke. Circulating platelets play an important role in the pathogenesis of these diseases. Platelets are anucleated cells with a complex cytoskeletal system, unique receptors, and specialized secretary granules. They are found in the circulation in high abundance, and respond to blood vessel injury by changing shape, secreting granular contents, and aggregation. This is advantageous in the regulation of physiological hemostasis, but can be unfavorable in pathological thrombosis. For this reason, understanding the mechanisms surrounding platelet aggregation is essential. Platelet function is tightly regulated by both pro- and anti-stimulatory mechanisms. Platelets are kept in an unstimulated state by little-known anti-stimulatory mechanisms. During vascular injury, pro-stimulatory mechanisms, such as signaling by various physiological agonists, override the anti-stimulatory machinery to achieve platelet aggregation. We have identified a novel platelet protein, ASK1, which appears to be a key participant in the pro-stimulatory mechanism. We hypothesize that ASK1 senses stress and/or pro-stimulatory signals initiated by agonists and transmits signals to the platelet fibrinogen receptor complex and helps in coordinating stimulatory signals that regulate platelet aggregation and thrombus formation. This proposal is focused on understanding the molecular mechanisms that are regulated by ASK1 in order to regulate platelet activation. The identification and characterization of such regulatory mechanisms may define new targets for developing potential therapeutic agents toward thrombotic disorders.

描述（由申请人提供）：人类死亡的首要原因是心血管疾病，如心肌梗死和中风。循环血小板在这些疾病的发病机制中起重要作用。血小板是一种无核细胞，具有复杂的细胞骨架系统、独特的受体和特化的分泌颗粒。它们在循环中大量存在，并通过改变形状、分泌颗粒状内容物和聚集来对血管损伤作出反应。这在生理止血的调节中是有利的，但在病理性血栓形成中可能是不利的。因此，了解血小板聚集的机制至关重要。血小板功能受到促刺激和抗刺激机制的严格调节。血小板通过鲜为人知的抗刺激机制保持在非刺激状态。在血管损伤期间，促刺激机制，例如通过各种生理激动剂的信号传导，超越抗刺激机制以实现血小板聚集。我们已经确定了一种新的血小板蛋白，ASK 1，这似乎是一个关键的参与者在促刺激机制。我们假设ASK 1感知由激动剂引发的应激和/或促刺激信号，并将信号传递给血小板纤维蛋白原受体复合物，并有助于协调调节血小板聚集和血栓形成的刺激信号。该提案的重点是了解由ASK 1调节以调节血小板活化的分子机制。这种调节机制的鉴定和表征可以定义用于开发针对血栓性疾病的潜在治疗剂的新靶点。