Targeting the Inflammasome to Prevent Thoracic Aortic Aneurysms and Dissections

针对炎症小体预防胸主动脉瘤和夹层

• 批准号: 9130437
• 负责人: SCOTT A LEMAIRE
• 金额: $ 39.63万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-04 至 2017-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9130437
• 关键词: Affect; Aorta; Aortic Aneurysm; Aortic Diseases; Binding; Biomechanics; C-terminal; Cardiovascular Diseases; Caspase; Caspase-1; Cause of Death; Cellular Stress; Cessation of life; Chest; Cleaved cell; Contractile Proteins; Data; Development; Disease; Disease Progression; Dissection; Extracellular Matrix; Failure; Foundations; Functional disorder; Gelatinase B; Glyburide; Goals; Health; Hereditary Disease; Human; In Vitro; Incidence; Knockout Mice; Knowledge; Life; Marfan Syndrome; Medial; Mediating; Mission; Modeling; Molecular; Multiprotein Complexes; Mus; Myosin Heavy Chains; N-terminal; Operative Surgical Procedures; Patients; Peptide Hydrolases; Play; Prevention; Procedures; Proteins; Public Health; Research; Research Personnel; Role; Rupture; Smooth Muscle Myocytes; Staging; Structure; Testing; Therapeutic Agents; Thoracic Aortic Aneurysm; Tissues; Tropomyosin; United States; Work; base; biological adaptation to stress; effective therapy; improved; in vivo; inhibitor/antagonist; innovation; mortality; prevent; repaired; research study; therapeutic target; treatment strategy

 DESCRIPTION (provided by applicant): Thoracic aortic aneurysms and dissections (TAAD) are interrelated cardiovascular diseases that carry high mortality. Current approaches to pharmacologic treatment of TAAD are ineffective, particularly in patients with sporadic disease not attributed to a genetic condition, such as Marfan syndrome. Although there is a critical need to develop new treatment strategies, a major barrier to this goal is a poor understanding of the molecular mechanisms that trigger and then promote aortic degeneration in sporadic TAAD. Therefore, the long-term goal of the investigators is to improve the understanding of the pathobiology of aortic wall degeneration in hope of developing new pharmacological strategies to prevent TAAD formation and progression. The overall objectives of this application are to determine the role of the NLRP3 inflammasome cascade, a multiprotein platform involved in amplifying intracellular stress responses, in promoting aortic destruction, and the extent to which this cascade represents a therapeutic target against TAAD. The central hypotheses are that the NLRP3-ASC- caspase-1 cascade promotes aortic degeneration by inciting protease-mediated extracellular matrix (ECM) destruction and promoting smooth muscle cell (SMC) contractile dysfunction, and that pharmacological inhibition of this cascade will prevent TAAD. These hypotheses will be tested through three specific aims: (1) Determine the effect of the inflammasome cascade on thoracic aortic wall structure and function, (2) Determine how the cascade promotes protease activation and SMC contractile dysfunction, and (3) Determine the extent to which pharmacological inhibition of the cascade prevents TAAD. Under the first aim, experiments using knockout mice will be conducted to determine whether the NLRP3 inflammasome cascade promotes aortic wall ECM destruction, contractile dysfunction and biomechanical failure. Under the second aim, studies with aortic SMCs will be performed to determine whether the cascade activates MMP-9 by directly cleaving two specific domains. In addition, protein interaction, cleavage, and contraction studies with SMCs will be conducted to determine whether the cascade promotes SMC contractile dysfunction by cleaving and degrading myosin heavy chain and tropomyosin. Under the third aim, experiments with two established mouse TAAD models will be conducted to determine whether pharmacological inhibitors of inflammasome activation (e.g. glyburide) will prevent TAAD development. The proposed research is significant because it will determine how the inflammasome cascade promotes TAAD development and the extent to which an inflammasome inhibitor can prevent TAAD. This research is innovative because it represents a new and substantive departure from the status quo, namely the current pharmacologic approaches to preventing sporadic TAAD progression. The development of a new, effective treatment would have an important positive impact by delaying or obviating invasive procedures in patients presenting with early-stage TAAD, suppressing disease progression in patients who are poor candidates for surgical treatment, and improving the durability of both open surgical and endovascular aortic repairs.

 描述（由申请人提供）：胸动脉瘤和疾病具有高度的TAAD药理学信任方法，尤其是在遗传状态下，例如触发Marfan综合征。长期目标是改善主动脉壁变性的tathobiology，以期制定新的药理学策略来防止TAAD和应用的进展主动脉灾难以及多大程度上 针对TAAD的级联靶标的是NLRP3-ASC-1级联反应通过煽动蛋白酶介导的细胞外基质（ECM）来促进主动脉症那里的目的是：（1）胸壁结构和功能上的炎性级别级联，（2）确定级联反应如何促进激活和SMC ILE功能障碍，确定nlrp3 firmascade的药理学的程度。在第二个目标下促进主动脉壁ECM的破坏，生物机械衰竭。结合级联是否通过裂解和降解肌球蛋白和tropomyosin来促进SMC收缩功能障碍。炎性抑制剂可以宣传。这项研究是创新的验证者，从现状进行了新的和实质性的偏离，以防止零星的TAAD进展。阶段的TAAD，抑制了候选手术和血管内主动脉维修的患者的疾病进展。