ROLE OF MYB FOR AIRWAY EPITHELIAL CELL DIFFERENTIATION

MYB 在气道上皮细胞分化中的作用

• 批准号: 9268062
• 负责人: Steven Brody
• 金额: $ 38.13万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-05-15 至 2019-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9268062
• 关键词: Address; Adult; Affect; Asthma; Basal Cell; Candidate Disease Gene; Cell Differentiation process; Cells; Chromatin; Chronic; Chronic Obstructive Airway Disease; Data; Development; Disease; Distal; Elements; Epithelial; Epithelial Cells; Epithelium; Failure; Gene Expression; Health; Human; In Vitro; Individual; Injury; Lead; Link; Lung; Lung diseases; Maintenance; Metaplasia; Mitotic; Modeling; Molecular; Mus; Natural regeneration; One-Step dentin bonding system; Pathogenesis; Pathologic; Pathway interactions; Population; Process; Proliferating; Role; Secretory Cell; Stem cells; Symptoms; Validation; airway epithelium; base; cdc Genes; cell type; cilium biogenesis; genome-wide; in vivo; injured airway; injury and repair; lung development; lung injury; mouse model; notch protein; novel; progenitor; programs; public health relevance; reconstitution; remediation; repaired; restoration; self-renewal; stem; transcription factor

 DESCRIPTION (provided by applicant): The pathways leading to airway epithelial cell differentiation and renewal are undergoing intense study as these programs are essential for repair following lung injury, and may be dysregulated leading to epithelial cell metaplasia in asthma and chronic obstructive airway disease. This project addresses the mechanism of normal restoration of the airway epithelium after injury. The current paradigm for airway epithelial cell regeneration is a one-step process, whereby regulatory factors direct a self-renewing P63+ progenitor cell to a differentiated type. In this project, we establish a new model based on our finding that the transcription factor Myb defines an essential intermediate stage in the progression from progenitor to specialized cell. Our findings suggest that the Myb+P63- cell is obligatory for the differentiation of a ciliated and secretory airway cell types. Myb is transietly expressed during lung development and in our primary-culture models, and is absent in the healthy adult lung. Myb is increased in our mouse models of lung injury and in airways of individuals with chronic obstructive lung disease. Depleting Myb in primary-culture of mouse and human airway epithelial cells abrogates differentiation. Accordingly, we generated mice with airway epithelial cell-specific deletion of Myb, and likewise found a failure to develop ciliated ad secretory cells. Genome-wide gene expression comparison between Myb deficient and sufficient cells identified programs for ciliated and secretory cell differentiation, and a reductin of Sox2 levels. Validation data demonstrated Sox2 was decreased in P63- airway epithelial cells, suggesting a Myb dependent requirement for Sox2. Together, these findings lead us to hypothesize that Myb regulates a program essential for the maintenance, repair and regeneration of differentiated airway epithelial cells. Using Myb targeted deficient mice and primary culture models, we propose to investigate (1) Myb-dependent cellular determinants for repair and regeneration using mouse injury models, and (2) identify Myb-dependent molecular programs for airway epithelial differentiation. The studies will establish a new model for understanding the pathogenesis of airways disease and define key elements as targets for reparative therapies.

 描述（由申请人提供）：气道上皮细胞分化和更新的主要途径正在进行深入研究，因为这些程序对于肺损伤后的修复至关重要，并且可能失调导致哮喘和慢性阻塞性气道疾病中的上皮细胞化生。该项目解决了损伤后气道上皮正常恢复的机制目前气道上皮细胞再生的范例是一步过程，因此调节因素指导自我更新。 P63+ 祖细胞分化为分化类型 在这个项目中，我们基于转录因子 Myb 定义了从祖细胞到特化细胞的过程中的一个重要中间阶段，建立了一个新模型。 Myb 对于纤毛细胞和分泌性气道细胞类型的分化是必需的，在肺发育期间和我们的原代培养模型中短暂表达，并且在我们的小鼠模型中健康成年肺中不存在。在小鼠和人类气道上皮细胞的原代培养物中去除 Myb 会消除肺损伤和慢性阻塞性肺疾病个体的气道分化。因此，我们产生了气道上皮细胞特异性删除 Myb 的小鼠，同样发现了失败。开发纤毛细胞和分泌细胞。Myb 缺陷细胞和充足细胞之间的全基因组基因表达比较确定了纤毛细胞和分泌细胞分化的程序，以及 Sox2 水平的降低。验证数据表明，P63-气道上皮细胞中的 Sox2 减少，表明对 Sox2 的 Myb 依赖性需求，这些发现使我们重新认识到 Myb 使用 Myb 调节分化气道上皮细胞的维持、修复和再生所必需的程序。针对缺陷小鼠和原代培养模型，我们建议研究（1）使用小鼠损伤模型进行修复和再生的 Myb 依赖性细胞决定因素，以及（2）确定 Myb 依赖性分子程序这些研究将建立一个新的模型来了解气道疾病的发病机制，并确定修复治疗目标的关键要素。