Basal cells in airway and alveolar remodeling

基底细胞在气道和肺泡重塑中的作用

• 批准号: 10615164
• 负责人: Barry R Stripp
• 金额: $ 60.5万
• 依托单位: CEDARS-SINAI MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-05-01 至 2026-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10615164
• 关键词: 3-Dimensional; Acceleration; Acute; Acute Lung Injury; Alveolar; Alveolus; Animal Model; Basal Cell; Basal Cell Hyperplasia; Behavior; Biological Assay; Cell Proliferation; Cell Transplantation; Cells; Cessation of life; ChIP-seq; Chemotaxis; Choristoma; Chronic lung disease; Clustered Regularly Interspaced Short Palindromic Repeats; Data; Development; Distal; Economic Burden; Epithelial Cells; Functional disorder; Genes; Genetic; Genetic Models; Goals; Human; Hyperplasia; Impairment; In Vitro; Individual; Infection; Inflammation; Influenza; Influenza A Virus, H1N1 Subtype; Injury; Intervention; LCN2 gene; Ligands; Link; Lung; Lung diseases; Mediating; Mitogens; Modeling; Molecular; Mus; Natural regeneration; Organoids; Pathway interactions; Patients; Play; Predisposition; Process; Proliferating; Protein Isoforms; Pulmonary Fibrosis; Regenerative capacity; Role; Secretory Cell; Serous; Site; Source; Specific qualifier value; Stratification; Structure of parenchyma of lung; Testing; Therapeutic; Tissues; Transfection; Viral Respiratory Tract Infection; Virus Diseases; WNT Signaling Pathway; Work; alveolar epithelium; cell injury; cell motility; cell type; epithelial stem cell; idiopathic pulmonary fibrosis; improved outcome; in vitro Model; in vivo; influenzavirus; injured; insight; knock-down; loss of function; lung injury; lung repair; mouse model; novel; programs; pulmonary function; pulmonary function decline; recruit; repaired; respiratory infection virus; severe injury; stem cell function; stem cells; three dimensional cell culture; transcription factor

Abstract Acute respiratory viral infections represent an enormous societal and economic burden with the potential for persistent declines in lung function among recovering patients. Severe infections trigger abnormal repair processes and inflammation leading to remodeling of small airways and alveoli, impaired pulmonary function and death in particularly susceptible individuals. These features of lung injury, repair and remodeling of small airways and alveoli, are recapitulated in mouse models of H1N1 influenza (PR8) virus infection, wherein alveolar injury leads to expansion of basal cells (BC) in airways and replacement of damaged alveolar epithelium. In preliminary studies we provide evidence that nascent BC are derived from a serous-like subset of airway secretory cells (intralobar serous or IS). We have identified an unexpected role for TAp63 in the specification of nascent BC and that Lcn2 expression by “activated” AT2 cells of the PR8-infected lung contributes to BC recruitment to injured alveoli. Finally, we show that recruitment of nascent BC to damaged alveolar regions impacts the proliferative activity and clonal behavior of surviving alveolar type 2 (AT2) cells. Aims of this proposal seek to test the overarching hypothesis that PR8-elicited nascent BC that ultimately colonize damaged alveolar regions are derived from IS cells through a fate transition that is regulated by TAp63. Furthermore, we hypothesize that AT2-derived Lcn2 mediates BC recruitment to injured alveoli where they regulate local Wnt signaling and inhibit AT2 cell proliferation. Aim 1 will examine the role of TAp63 and its downstream targets in IS>BC specification following PR8-induced lung injury. Aim 2 will investigate roles for AT2-derived Lcn2 in recruitment of PR8-elicited BC to injured alveoli. Aim 3 will test the hypothesis that nascent BC recruited to sites of parenchymal injury suppress the regenerative capacity of surviving AT2 cells and will explore roles for BC- derived Wnt ligands in this process. Completion of these aims will provide new insights into cellular and molecular mechanisms of repair in acute lung injury and how persistent activation of these repair pathways might contribute to tissue remodeling in lung disease.

抽象的 急性呼吸道病毒感染造成巨大的社会和经济负担，并有可能造成 康复中的患者肺功能持续下降。严重感染引发异常修复 过程和炎症导致小气道和肺泡重塑，肺功能受损 以及特别易感人群的死亡。肺损伤、修复和重塑的这些特征 在 H1N1 流感 (PR8) 病毒感染的小鼠模型中重现了气道和肺泡，其中肺泡 损伤导致气道中基底细胞（BC）扩张并替换受损的肺泡上皮。在 初步研究，我们提供证据表明新生 BC 源自气道的浆液样子集 分泌细胞（叶内浆液性或IS）。我们发现 TAp63 在规范中具有意想不到的作用 新生 BC 以及 PR8 感染肺的“激活”AT2 细胞的 Lcn2 表达有助于 BC 募集到受伤的肺泡。最后，我们表明新生 BC 募集到受损的肺泡区域 影响存活肺泡 2 型 (AT2) 细胞的增殖活性和克隆行为。本提案的目的 试图检验 PR8 引发新生 BC 最终定植受损肺泡的总体假设 这些区域是通过 TAp63 调节的命运转变衍生自 IS 细胞。此外，我们 假设 AT2 衍生的 Lcn2 介导 BC 募集至受损肺泡，并在其中调节局部 Wnt 信号传导并抑制 AT2 细胞增殖。目标 1 将研究 TAp63 及其下游靶点在 PR8 诱导的肺损伤后 IS>BC 规范。目标 2 将研究 AT2 衍生的 Lcn2 在 PR8 引起的 BC 募集到受伤的肺泡中。目标 3 将检验新生 BC 招募到站点的假设 实质损伤抑制存活 AT2 细胞的再生能力，并将探索 BC- 的作用 在此过程中衍生出Wnt配体。这些目标的完成将为细胞和分子提供新的见解 急性肺损伤的修复机制以及这些修复途径的持续激活如何发挥作用 肺部疾病中的组织重塑。