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Notch signaling-mediated functions of airway eosinophils in lung disease

Notch信号介导的气道嗜酸性粒细胞在肺部疾病中的功能

基本信息

批准号：
8594256
负责人：
Lisa Ann Spencer
金额：
$ 41.23万
依托单位：
BETH ISRAEL DEACONESS MEDICAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-01-18 至 2015-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8594256
关键词：
Antigen-Presenting Cells Antigens Asthma CD4 Positive T Lymphocytes Cell Survival Cells Chemotaxis Cytokine Signaling Data Development Disease Disease Progression Eosinophilia Goals Human Hypersensitivity Immune Immunity Inflammatory Interleukin-4 Investigation Laboratories Lead Leucocytic infiltrate Leukocytes Ligands Longevity Lung Lung diseases Mediating Microscopic Mus Notch Signaling Pathway Ovalbumin Pathogenesis Pathway interactions Phase Receptor Activation Research Design Research Personnel Resolution Role Shapes Signal Transduction Signal Transduction Pathway Stimulus T-Lymphocyte Tacrine airway hyperresponsiveness airway remodeling asthmatic airway base cytokine design eosinophil immunoregulation in vivo insight mouse model new therapeutic target notch protein novel public health relevance receptor response therapeutic target

项目摘要

DESCRIPTION (provided by applicant): Eosinophils are innate immune leukocytes associated with asthma, allergies and other diseases. Despite the long recognition of eosinophilic involvement in asthma, specific, non-redundant roles for eosinophils in disease pathogenesis had been elusive. However, recent studies from several laboratories have revealed new functions of eosinophils in immunomodulation and airway remodeling, changing the classic paradigm of disease pathogenesis and reinvigorating the field with a promise of more specific therapeutic targets. Our overall goal is to identify and mechanistically define effector functions of eosinophils vital to the initiation and exacerbation of asthma. In line with this goal, this proposal builds upon our novel discovery that mature human eosinophils express fully functional Notch ligands and receptors, indicating eosinophils utilize Notch signaling pathways, both as signal-receiving "target" cells and as signal- sending "signaling" cells. Our preliminary data establishes our overlying hypothesis that Notch signaling underlies eosinophil functions critical to asthma. Our studies will specifically investigate two hypotheses: 1) Notch receptor activation is required in parallel with cytokine signals to achieve full and sustained activation of eosinophils in asthmatic airways; and 2) Eosinophils promote a Th2 milieu in asthma by Notch ligand-mediated juxtacrine interactions with T cells. While experimental approaches utilize predominantly human eosinophils, proposed studies also take full advantage of the manipulative benefits of mouse models. Our proposal may provide vital insights into the mechanistic basis for eosinophil functions pertinent to asthma, and by extension other inflammatory diseases of the lung involving eosinophilia, relevant to development of novel, targeted therapeutic approaches.

描述（由申请人提供）：嗜酸性粒细胞是与哮喘、过敏和其他疾病相关的先天免疫白细胞。尽管嗜酸性粒细胞参与哮喘的认识由来已久，但嗜酸性粒细胞在疾病发病机制中的特异性、非冗余性作用一直是难以捉摸的。然而，最近几个实验室的研究揭示了嗜酸性粒细胞在免疫调节和气道重塑中的新功能，改变了疾病发病机制的经典范式，并为该领域带来了更特异性治疗靶点的希望。我们的总体目标是确定和机制定义的嗜酸性粒细胞的效应功能至关重要的启动和哮喘的恶化。与该目标一致，该提议建立在我们的新发现之上，即成熟的人嗜酸性粒细胞表达完全功能性Notch配体和受体，表明嗜酸性粒细胞利用Notch信号传导途径，既作为信号接收“靶”细胞又作为信号发送“信号传导”细胞。我们的初步数据建立了我们的假设，即Notch信号转导是哮喘关键的嗜酸性粒细胞功能的基础。我们的研究将具体调查两个假设：1）Notch受体激活需要与细胞因子信号并行，以实现哮喘气道中嗜酸性粒细胞的完全和持续激活; 2）嗜酸性粒细胞通过Notch配体介导的嗜酸性粒细胞与T细胞的相互作用促进哮喘中的Th 2环境。虽然实验方法主要利用人类嗜酸性粒细胞，但拟议的研究也充分利用了小鼠模型的操纵优势。我们的建议可能会提供重要的洞察力的机制基础嗜酸性粒细胞的功能相关的哮喘，并通过扩展其他炎症性疾病的肺部涉及嗜酸性粒细胞增多症，相关的发展新的，有针对性的治疗方法。