Transcriptional Programming of Asthma Related Pathology in Respiratory Epithelia

呼吸道上皮细胞中哮喘相关病理学的转录编程

• 批准号: 8650303
• 负责人: Jeffrey A Whitsett
• 金额: $ 51.8万
• 依托单位: CINCINNATI CHILDRENS HOSP MED CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-04-01 至 2018-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8650303
• 关键词: Acute; Affect; Allergens; Alternative Splicing; Asthma; Biochemical; Biochemistry; Bioinformatics; Cell Differentiation process; Cells; Cellular biology; ChIP-seq; Chronic; Chronic Obstructive Airway Disease; Chronic lung disease; Clinical; Data; Databases; Development; Diagnosis; Disease; Economic Burden; Epithelial; Epithelial Cells; Exposure to; Family member; Functional RNA; Funding; Gene Expression; Gene Expression Regulation; Genes; Genetic; Genetic Transcription; Goblet Cells; Health; Homeostasis; Host Defense; Human; Hyperactive behavior; Hyperplasia; Immune response; In Vitro; Infection; Inflammation; Inflammatory; Inflammatory Response; Interleukin-13; Laboratories; Literature; Lung; Lung Inflammation; Lung diseases; Mediating; Metaplasia; Modeling; Morbidity - disease rate; Mucous body substance; Mus; Natural Immunity; Pathogenesis; Pathology; Patients; Phosphorylation; Physiological; Physiology; Play; Pneumonia; Process; Production; RNA; RNA Sequences; Recovery; Regulation; Regulator Genes; Respiration Disorders; Respiratory physiology; Rhinovirus; Role; Signal Transduction; Structure; Structure of respiratory epithelium; Systems Biology; Testing; Tissues; Transcriptional Activation; Transcriptional Regulation; Transgenic Mice; Virus Diseases; Work; airborne allergen; airway inflammation; airway remodeling; base; chemokine; chromatin immunoprecipitation; cytokine; health economics; in vivo; insight; interest; microbial; mortality; mouse model; mutant; novel; pathogen; programs; public health relevance; repaired; research study; respiratory; respiratory virus; response; thyroid transcription factor 1; trafficking; transcription factor

DESCRIPTION (provided by applicant): This renewal application seeks funding to define a transcriptional network that determines AEC differentiation, goblet cell metaplasia/hyperplasia, and inflammation related to the pathogenesis of asthma, other chronic pulmonary disorders, and acute viral infection by rhinovirus. The application is based on novel data demonstrating the critical roles of the proposed transcriptional network that is centered on an Ets family member, SPDEF (SAM pointed domain ets-like factor) that regulates goblet cell differentiation and inflammatory processes in the lung. Our preliminary data demonstrate that differentiation of AECs in conducting airways is mediated by a cell intrinsic transcriptional program in which SPDEF and FOXA family members and TTF-1 (thyroid transcription factor-1, aka Nkx2.1) play fundamental roles. Preliminary data support the concept that Spdef drives mucus cell metaplasia, eosinophilic chemokine, and TH2 cytokine expression from AECs in response to allergens and rhinoviral infection. The application will utilize transgenic mouse models in which Spdef is deleted or expressed; bioinformatics, in vitro cultures of human bronchial epithelial cell (HBECs), and biochemistry to determine mechanisms by which SPDEF controls mucus metaplasia and innate immunity. Aim 1 will identify the mechanisms by which the transcription factor SPDEF is regulated at transcriptional and post-transcriptional levels during mucus metaplasia induced by rhinovirus and aeroallergen exposure. Mechanisms controlling its regulation and function will be identified. Aim 2 will test the hypothesis that SPDEF regulates transcription of genes critical for mucus cell differentiation, innate immunity, and inflammation i the respiratory epithelium, identifying transcriptional targets in AECs. Aim 3 will identify physiological and inflammatory consequences of SPDEF in mouse models in vivo, identifying the effects of the network on pulmonary physiology, inflammatory responses, and tissue remodeling during viral infection and TH2 stimulation. The present application represents my laboratory's increasing interest in the transcriptional control of conducting airway epithelial cel differentiation in health and disease. These studies will provide insights into the pathogenesis of mucus cell metaplasia and hyperproduction associated with asthma, COPD, and acute infections that commonly complicate these disorders, providing the basis for the development of new strategies to diagnose and treat chronic respiratory diseases that are common causes of morbidity and mortality world- wide.

描述（由申请人提供）：本更新申请寻求资金以定义一个转录网络，该网络确定AEC分化、杯状细胞化生/增生以及与哮喘、其他慢性肺部疾病和鼻病毒急性病毒感染发病机制相关的炎症。该应用基于新的数据，证明了所提出的转录网络的关键作用，该转录网络以Ets家族成员SPDEF（SAM指向结构域ets样因子）为中心，调节肺中的杯状细胞分化和炎症过程。我们的初步数据表明，传导气道中AEC的分化是由细胞内在转录程序介导的，其中SPDEF和FOXA家族成员以及TTF-1（甲状腺转录因子-1，又名Nkx2.1）发挥着重要作用。初步数据支持Spdef驱动粘液细胞化生、嗜酸性粒细胞趋化因子和TH 2细胞因子从AEC表达以响应过敏原和鼻病毒感染的概念。该申请将利用Spdef缺失或表达的转基因小鼠模型;生物信息学，人支气管上皮细胞（HBEC）的体外培养物和生物化学来确定SPDEF控制粘液化生和先天免疫的机制。目的1将确定在鼻病毒和空气过敏原暴露诱导的粘液化生过程中转录因子SPDEF在转录和转录后水平的调节机制。将确定控制其调节和功能的机制。目的2将检验SPDEF调节呼吸道上皮中对粘液细胞分化、先天免疫和炎症至关重要的基因转录的假设，确定AEC中的转录靶点。目的3将确定SPDEF在体内小鼠模型中的生理和炎症后果，确定病毒感染和TH 2刺激期间网络对肺生理学，炎症反应和组织重塑的影响。本申请代表了我的实验室对健康和疾病中进行气道上皮细胞分化的转录控制的日益增长的兴趣。这些研究将提供深入了解的发病机制， 与哮喘、慢性阻塞性肺病和急性感染相关的粘液细胞化生和过度分泌，这些疾病通常使这些疾病复杂化，为诊断和治疗慢性呼吸道疾病的新策略的发展提供了基础，这些疾病是世界范围内发病和死亡的常见原因。