Regulation of Proinflammatory Signaling Pathways in CFTR

CFTR 中促炎信号通路的调节

• 批准号: 7477883
• 负责人: Harvey Bruce Pollard
• 金额: $ 29.52万
• 依托单位: HENRY M. JACKSON FDN FOR THE ADV MIL/MED
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-06-15 至 2011-08-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7477883
• 关键词: Affect; Affinity; Antibodies; Binding; Binding Proteins; Biology; Biopsy; Cell Death; Cell Line; Cell Nucleus; Cells; Chemicals; Chemistry; Chronic; Complex; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA; DNA Sequence; Data; Disease; Doctor of Medicine; Doctor of Philosophy; Epithelial Cells; Epithelium; Ethanol; Formaldehyde; Freezing; Gelshift Analysis; Gene Transfer; Genes; Gland; Goals; Heating; Heterogeneous-Nuclear Ribonucleoproteins; IL8 gene; In Vitro; Individual; Infection; Inflammatory; Informatin; Investigation; Laboratories; Length; Life; Location; Lung; Maps; Mass Spectrum Analysis; Methods; Microarray Analysis; Microdissection; Molecular; Mutate; Mutation; NF-kappa B; Nuclear Extract; Nuclear Protein; Nuclear Proteins; Obstruction; Phenotype; Property; Protein Binding; Protein Microchips; Proteins; Proteomics; Radiolabeled; Recovery; Regulation; Research Personnel; Respiratory physiology; Sampling; Signal Pathway; Signal Transduction; Structure of parenchyma of lung; Surface; System; Technology; Testing; Tissues; airway inflammation; aqueous; base; cis acting element; crosslink; cystic fibrosis patients; disorder control; experience; hnRNP A1; in vivo; innovation; link protein; mutant; programs; promoter; protein function; radiotracer; reconstitution; repaired

DESCRIPTION (provided by applicant): Cystic fibrosis (CF) is the most common fatal autosomal recessive disease in the U.S., and is due to mutations in the CFTR gene. CF is characterized by constitutive hypersecretion of proinflammatory IL-8 from airway epithelial cells, and death usually ensues from chronic airway inflammation and loss of lung function. Our long term goal has therefore been to identify the mechanisms by which CFTR mutations cause constitutive IL-8 secretion from CF lung epithelial cells. Our approach is to identify the proteins which bind to the IL-8 promoter in CF lung epithelial cells, and to determine which one(s) might be responsible for the hyper-productive IL-8 phenotype. Preliminary data show that NFkappaB signaling is critical for IL-8 promoter activity in CF cells. In addition, we find that the protein hnRNP[A2B1] binds to the IL-8 promoter, affects NFkappaB action, and further activates IL-8 expression in CF cells. Based on these and other preliminary data we have hypothesized that hnRNP[A2B1], and possibly other proteins binding to the IL-8 promoter, are responsible for regulating constitutive, NFkappaB-dependent hyperexpression of IL-8 in CF lung epithelial cells. To test this hypothesis in vitro and in vivo, we propose the following specific aims: Specific Aim1: To identify proteins which bind to the IL-8 promoter in CF lung epithelial cells, and to determine their mechanisms of action on IL-8 expression. We will use mass spectrometry and crosslinking studies to identify and chemically validate proteins in nuclear extracts of CF lung epithelial cells which bind to the 167 bp IL-8 promoter DNA. Specific Aim 2: To map the locations and determine the molecular mechanism of interaction for proteins binding to the IL-8 promoter in CF lung epithelial cells. We will test the ability of free wildtype and mutant IL-8 promoter DNA sequences to competitively displace proteins from immobilized IL-8 promoter DNA. Specific Aim 3: To investigate the ensemble of proteins associated with the IL-8 promoter in bronchial lung epithelial cells from CF patients. We will prepare nuclear extracts from expanded cultures of CF and non-CF disease control bronchial brush biopsies of CF patients, and determine the proteins which bind to the IL-8 DNA promoter sequence. Significance, innovation, and uniqueness: This proposal is significant in that successful completion will determine those dysfunctional signaling pathway proteins which are responsible, directly or indirectly, for the proinflammatory lung phenotype of CF. The proposal is both unique and innovative by directing the investigation to the biology and chemistry of the IL-8 promoter in CF lung epithelial cells, both in vitro and in vivo.

描述(申请人提供)：囊性纤维化(CF)是美国最常见的致命性常染色体隐性遗传病，由CFTR基因突变引起。慢性支气管炎的特征是呼吸道上皮细胞结构性高分泌促炎性IL-8，死亡通常是由于慢性呼吸道炎症和肺功能丧失所致。因此，我们的长期目标是确定CFTR突变导致CF肺上皮细胞结构性IL-8分泌的机制。我们的方法是在肺上皮细胞中鉴定与IL-8启动子结合的蛋白质，并确定哪一个(S)可能与高产量的IL-8表型有关。初步数据表明，NFkappaB信号通路对CF细胞中IL-8启动子的活性至关重要。此外，我们还发现hnRNP[a2b1]蛋白与IL-8启动子结合，影响NFkappaB的作用，并进一步激活CF细胞中IL-8的表达。基于这些和其他初步数据，我们假设hnRNP[a2b1]，以及可能与IL-8启动子结合的其他蛋白质，负责调节CF肺上皮细胞中依赖于NFkappaB的结构性IL-8的高表达。为了在体外和体内验证这一假说，我们提出了以下具体目标：特异性目的1：在肺上皮细胞中鉴定与IL-8启动子结合的蛋白，并确定它们对IL-8表达的作用机制。我们将使用质谱仪和交联剂研究来鉴定和化学验证与167bpIL-8启动子DNA结合的肺泡巨噬细胞核提取液中的蛋白质。特异目的2：定位肺上皮细胞中IL-8启动子结合蛋白的位置并确定其相互作用的分子机制。我们将测试游离野生型和突变型IL-8启动子DNA序列竞争性置换固定化IL-8启动子DNA中的蛋白质的能力。特异性目的3：研究慢性阻塞性肺疾病患者支气管肺上皮细胞中与IL-8启动子相关的蛋白质集合。我们将从CF和非CF疾病对照患者的支气管刷活检组织中制备核提取液，并确定与IL-8 DNA启动子序列结合的蛋白质。重要性、创新性和独特性：这一建议具有重要意义，因为成功完成这项研究将确定那些功能失调的信号通路蛋白，这些蛋白直接或间接地导致CF的促炎肺表型。该方案通过在体外和体内对CF肺上皮细胞中IL-8启动子的生物学和化学的研究，既是独特的，也是创新的。