Role of Adenosine in Allergic Lung Disease

腺苷在过敏性肺病中的作用

基本信息

项目摘要

DESCRIPTION (provided by applicant): Elevated adenosine levels in the lungs and exhaled breath of asthmatics, with further increases following antigen challenge, suggests that this ubiquitous mediator may contribute to the pathophysiology of asthma. Many of the effects of adenosine in the asthmatic lung are mast cell-dependent. Adenosine has both pro- and anti-inflammatory effects on mast cells, due to the expression of multiple adenosine receptors on the cell surface, each capable of activating very different intracellular signaling pathways. In this proposal we will test the hypothesis that both pro- and anti-inflammatory signals are transmitted to the mast cell by adenosine via the activation of distinct cell-surface receptors, and that engagement of these receptors by adenosine influences AHR, inflammatory cell influx, and airway remodeling. In aim 1 we will investigate the pro- inflammatory role of A3 receptors on mast cells in AHR, airway inflammation, and remodeling. In aim 2 we will investigate the capacity of agonist-induced activation of Gs-coupled adenosine receptors to limit AHR, airway inflammation, and remodeling. In aim 3 we will investigate constitutive activity of the A2B receptor. For all aims we will conduct in vitro experiments with human mast cells as well as mechanistic in vivo experiments using a series of models lacking adenosine receptors on mast cells. Completion of these aims will define pro- vs. anti-inflammatory signaling pathways on the mast cell, and identify the mechanisms by which adenosine- induced mast cell activation contributes to the cardinal features of asthma. PUBLIC HEALTH RELEVANCE. Asthma is a common chronic disease affecting approximately 10% of people in the United States. A better understanding of the inflammatory mediators involved in this disease, such as adenosine, will help identify new avenues of therapy, leading to better treatments for asthma.
描述(由申请人提供):哮喘患者肺部和呼出气体中腺苷水平升高,并在抗原激发后进一步升高,表明这种普遍存在的介质可能参与哮喘的病理生理。腺苷在哮喘肺中的许多作用是肥大细胞依赖性的。腺苷对肥大细胞具有促炎和抗炎作用,这是由于细胞表面有多个腺苷受体表达,每个受体都能激活非常不同的细胞内信号通路。在本提案中,我们将验证以下假设:促炎和抗炎信号都是通过腺苷激活不同的细胞表面受体传递到肥大细胞的,腺苷参与这些受体会影响AHR、炎症细胞内流和气道重塑。在目的1中,我们将研究A3受体对肥大细胞在AHR、气道炎症和重塑中的促炎作用。在目的2中,我们将研究激动剂诱导的gs偶联腺苷受体激活限制AHR、气道炎症和重塑的能力。在目标3中,我们将研究A2B受体的组成活性。为了所有的目的,我们将对人类肥大细胞进行体外实验,并使用一系列肥大细胞上缺乏腺苷受体的模型进行体内机制实验。这些目标的完成将定义肥大细胞上的促炎与抗炎信号通路,并确定腺苷诱导肥大细胞激活有助于哮喘主要特征的机制。公共卫生相关性。哮喘是一种常见的慢性疾病,在美国大约有10%的人患有哮喘。更好地了解这种疾病中涉及的炎症介质,如腺苷,将有助于确定新的治疗途径,从而更好地治疗哮喘。

项目成果

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STEPHEN Lloyd TILLEY其他文献

STEPHEN Lloyd TILLEY的其他文献

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{{ truncateString('STEPHEN Lloyd TILLEY', 18)}}的其他基金

Adenosine receptors as therapeutic targets for chronic rhinosinusitis
腺苷受体作为慢性鼻窦炎的治疗靶点
  • 批准号:
    8415507
  • 财政年份:
    2012
  • 资助金额:
    $ 36.88万
  • 项目类别:
Lung Desease Models Core
肺部疾病模型核心
  • 批准号:
    7977207
  • 财政年份:
    2009
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    7822528
  • 财政年份:
    2009
  • 资助金额:
    $ 36.88万
  • 项目类别:
Lung Desease Models Core
肺部疾病模型核心
  • 批准号:
    7476122
  • 财政年份:
    2008
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of propionibacteria in sarcoidosis
丙酸杆菌在结节病中的作用
  • 批准号:
    6941641
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    6729839
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    6987162
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    7667775
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    7882355
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:
Role of Adenosine in Allergic Lung Disease
腺苷在过敏性肺病中的作用
  • 批准号:
    6839463
  • 财政年份:
    2004
  • 资助金额:
    $ 36.88万
  • 项目类别:

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