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Expression and Modulation of Mast Cell Function in Asthma

哮喘中肥大细胞功能的表达和调节

基本信息

批准号：
8072934
负责人：
Stephen Joseph Galli
金额：
$ 8.32万
依托单位：
STANFORD UNIVERSITY
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：
2010-08-03 至 2011-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8072934
关键词：
2,4-Dinitrophenol Abbreviations Acute Affinity Allergic inflammation Aluminum Hydroxide Alveolar Antibodies Antigens Asthma Bone Marrow Bromodeoxyuridine C57BL/6 Mouse Cell physiology Cells Chronic Chymase Congenic Mice Contact hypersensitivity Cytotoxic T-Lymphocytes Dependence Dermal Development Dinitrophenols Disease Management Endothelin-1 Enzymes Experimental Autoimmune Encephalomyelitis Fluorescein Fluorescein-5-isothiocyanate Fluoresceins Functional disorder Funding G-Protein-Coupled Receptors Guanine Nucleotide Exchange Factors Hematoxylin and Eosin Staining Method Histocytochemistry Human IgE Receptors Individual Inflammation Inflammatory Response Interferon Type II Interferons Interleukin-3 Irrigation Isothiocyanates Knock-in Mouse Knock-out Leukocytes Leukotrienes Lung Major Histocompatibility Complex Mediation Membrane Modeling Monoclonal Antibodies Mus Mutant Strains Mice Nose Nucleotides Ovalbumin Oxazolone Passive Cutaneous Anaphylaxis Peritoneal Process Proto-Oncogene Protein c-kit Protocols documentation Resistance Role Serum Albumin Stem Cell Factor T-Cell Receptor TNF gene Testing Tissues Tumor Necrosis Factor-alpha Tumor Necrosis Factors Venous Wild Type Mouse airway hyperresponsiveness aluminum sulfate cell type embryonic stem cell eosinophil in vivo mast cell methacholine mouse model mutant neutrophil novel strategies progenitor progesterone 11-hemisuccinate-(2-iodohistamine)receptor response small hairpin RNA

项目摘要

DESCRIPTION (provided by applicant): We hypothesize that mast cells (MCs) can have direct and indirect effects which can significantly enhance the local development of antigen- (Ag-) induced inflammatory responses in the airways, as well as the structural and functional consequences of such processes in the lungs. Specifically, we hypothesize that, in certain mouse models of acute or chronic allergic inflammation involving the lungs, MC activation by both antibody- (Ab-)dependent and Ab-independent mechanisms results in net effects which can contribute significantly to the development and/or enhancement of the inflammation, airway hyperreactivity (AHR) and tissue remodeling associated with these "asthma models", and that many such effects are promoted by MC- associated TNF and can be enhanced by interferon gamma (IFNgamma), acting via IFNgamma receptors (IFNgammaRs) on MCs. We will test these hypotheses by using different protocols that can elicit either acute or chronic models of asthma in mice. We will examine genetically MC-deficient c-kit mutant mice (WBB6F1-KitW/W-v mice and C57BL/6- KitW-sh/W-sh mice) the congenic Kit+/+ wild type (WT) mice and "MC knock-in mice", i.e., c-kit mutant mice which have been selectively engrafted with WT MCs or MCs which express genetically-determined abnormalities in the expression of products which we hypothesize are involved in the activation, modulation or mediation of MC function. By assessing the extent to which key features of these asthma models differ in c-kit mutant MC-deficient and WT mice, we can quantify the c-kit-dependence of the responses. By determining to what extent any abnormalities in the expression of the responses in c-kit mutant mice are "normalized" or otherwise altered when such mice have been selectively engrafted with WT or genetically-manipulated MCs, we can assess the contribution of MCs, as well as individual MC products, including membrane-associated or soluble TNF, IFNgammaR1 or certain G protein-coupled receptors, to the expression of these features of the responses. By understanding better the mechanisms by which MCs can enhance the development of important features of asthma models in mice, and the mechanisms which influence the extent to which MCs can be activated to express their function in these settings, we will broaden the view of the potential roles of MCs in the development and progression of asthma in humans, and perhaps suggest new approaches for the management of this disorder.

描述（由申请人提供）：我们假设肥大细胞（MC）可具有直接和间接作用，其可显著增强气道中抗原（Ag）诱导的炎症反应的局部发展，以及肺中此类过程的结构和功能后果。具体而言，我们假设，在涉及肺的急性或慢性过敏性炎症的某些小鼠模型中，通过抗体（Ab）依赖性和Ab非依赖性机制的MC活化导致净效应，其可显著促进与这些“哮喘模型”相关的炎症、气道高反应性（AHR）和组织重塑的发展和/或增强，并且许多这样的作用被MC相关的TNF促进，并且可以被干扰素γ（IFN γ）增强，通过IFN γ受体（IFN γ R）作用于MC。我们将通过使用不同的方案来测试这些假设，这些方案可以在小鼠中诱发急性或慢性哮喘模型。我们将检查遗传上MC缺陷的c-kit突变小鼠（WBB 6 F1-KitW/W-v小鼠和C57 BL/6- KitW-sh/W-sh小鼠）、同源Kit+/+野生型（WT）小鼠和“MC敲入小鼠”，即，c-kit突变小鼠，其已经选择性地移植了WT MC或在我们假设参与MC功能的激活、调节或介导的产物的表达中表达遗传确定的异常的MC。通过评估这些哮喘模型的关键特征在c-kit突变MC缺陷小鼠和WT小鼠中的差异程度，我们可以量化反应的c-kit依赖性。通过确定当c-kit突变小鼠被选择性移植WT或遗传操作的MC时，这些小鼠中应答表达的任何异常被“正常化”或以其他方式改变的程度，我们可以评估MC以及单个MC产物的贡献，包括膜相关或可溶性TNF、IFN γ R1或某些G蛋白偶联受体，这些反应的特征。通过更好地了解MCs可以促进小鼠哮喘模型重要特征发展的机制，以及影响MCs在这些环境中被激活表达其功能的程度的机制，我们将拓宽MCs在人类哮喘发展和进展中的潜在作用的视野，并可能提出管理这种疾病的新方法。