课题基金 / 基金详情

Surfactant Proteins and NO in Inflammatory Disease

Surfactant Proteins and NO in Inflammatory Disease
炎症性疾病中的表面活性蛋白和 NO
批准号:
7116878
负责人:
Andrew J Gow
金额:
$34.67万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-30 至 2008-08-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The major goal of this research project is to investigate how NO chemistry plays a role both in the initiation and in the propagation of inflammatory disease within the lung. In particular, we will investigate the effects of altered NO chemistry within an animal model of pulmonary inflammation, ablation of the SP-D gene. Mice lacking the SP-D gene develop a non-specific inflammatory disease within the lung in the absence of an infectious agent. This disease is characterized by parenchymal infiltrates and peribronchial neutrophilial lipoproteinosis, and alterations in the NO chemistry of the lung (loss of S-nitrosothiol, SNO, and gain of nitrotyrosine within tissue and a relative greater increase of nitrates within the bronchiolar alveolar lavage, BAL). Therefore, this animal model provides an ideal opportunity to investigate the role that NO plays in pulmonary inflammation. We will use both pharmacological and genetic interventions to manipulate NO production within this model and examine the effects of these manipulations upon the development of disease. Furthermore, we propose that the loss of normal signaling NO is part of this pathology, therefore, we will investigate the possible use of inhaled NO or its redox congener, ethyl nitrite, in treatment of pulmonary inflammation, in order to further our understanding of the molecular mechanisms involved in pulmonary inflammatory disease, and how NO modifies these mechanisms, we will examine the potential protein targets of reactive species both within the tissue and the lavage, in particular, we will assess the production of nitrated proteins, S-nitrosylated proteins, and oxidized proteins. Such experiments may lead to valuable information concerning the physiological signaling pathways of reactive species and how these pathways are altered during inflammation. Finally, we will examine how rescue of the phenotype by purified SP-D may be affected by NO-mediated modifications of SP-D. These experiments wilt provide valuable information as to how SP-D and NO are involved in the maintenance of physiological pulmonary function.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
Nitric Oxide and Cellular Maturity Are Key Components of Pro-Inflammatory Cytokine-Induced Apoptosis of Human Fetal Lung Epithelial Cells.
一氧化氮和细胞成熟是促炎细胞因子诱导的人胎儿肺上皮细胞凋亡的关键组成部分。
DOI: 10.2174/1874085501103010001
发表时间: 2011
期刊: The open cell development & biology journal
影响因子: --
作者: [Posencheg,MichaelA, Gow,AndrewJ, Wang,Ping, Gonzales,LindaW, Guo,Changjiang]
通讯作者: Guo,Changjiang
DOI: 10.1513/pats.200506-058bg
发表时间: 2006-04-01
期刊: Proceedings of the American Thoracic Society
影响因子: --
作者: [Gow, Andrew J]
通讯作者: Gow, Andrew J
SP-D-dependent regulation of NO metabolism in lipopolysaccharide-stimulated peritoneal macrophages.
脂多糖刺激的腹膜巨噬细胞中 NO 代谢的 SP-D 依赖性调节。
DOI: 10.1007/s10517-009-0525-z
发表时间: 2009
期刊: Bulletin of experimental biology and medicine
影响因子: 0.7
作者: [Atochina-Vasserman,EN, Abramova,EV, Tomer,Y, Scott,P, Nazarov,VA, Kruglov,SV, Beers,MF, Gow,AJ, Malyshev,IYu]
通讯作者: Malyshev,IYu
2023 Nitric Oxide GRC and GRS
  • 批准号:
    10608028
  • 项目类别:
  • 资助金额:
    $1.5万
  • 财政年份:
    2023
  • 负责人:
    Andrew J Gow
  • 依托单位:
Obstructive Sleep Apnea and WTC dust: Does Chronic Intermittent Hypoxia exacerbate WTC dust induced lung injury
Obstructive Sleep Apnea and WTC dust: Does Chronic Intermittent Hypoxia exacerbate WTC dust induced lung injury
NO-Modified Biomolecules and Pulmonary Signaling
  • 批准号:
    8707538
  • 项目类别:
  • 资助金额:
    $33.65万
  • 财政年份:
    2008
  • 负责人:
    Andrew J Gow
  • 依托单位:
海外基金