Regulation of alveolar epithelial homeostasis in acute lung injury

急性肺损伤中肺泡上皮稳态的调节

• 批准号: 9000737
• 负责人: Jieru Wang
• 金额: $ 23.93万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-04-15 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9000737
• 关键词: AIM2 gene; Acute Lung Injury; Allergic Disease; Alveolar; Alveolar Macrophages; Animal Model; Asthma; Bacteria; Cell Communication; Cell Culture System; Cells; Cessation of life; Child; DNA Virus Infections; Data; Diffuse; Disease; Distal; Economics; Epithelial; Epithelial Cells; Gases; Goals; Homeostasis; Hospitalization; Host Defense; Human; Immune response; Impairment; In Vitro; Infection; Influenza; Influenza A Virus, H1N1 Subtype; Injury; Interleukin-1 beta; Laboratories; Lower respiratory tract structure; Lung; Manuscripts; Measures; Mediating; Molecular; Mus; Pathogenicity; Patients; Play; Primary Cell Cultures; Production; Public Health; Pulmonary Edema; RNA Virus Infections; Regulation; Role; Small Interfering RNA; System; Therapeutic Agents; Tight Junctions; Tissues; Type II Epithelial Receptor Cell; Viral; Virus; Virus Activation; Virus Diseases; cell type; cytokine; improved; in vivo; in vivo Model; influenzavirus; injury and repair; macrophage; mortality; mouse model; novel; novel therapeutics; pandemic disease; pandemic influenza; repaired; seasonal influenza; transmission process; treatment strategy; young adult

DESCRIPTION (provided by applicant): This project aims to determine how human lung epithelial homeostasis is regulated in acute lung injury induced by the 2009 H1N1 pandemic influenza virus. Because of the rapid transmission and high potential for increased pathogenicity of the H1N1 pandemic virus, there is an urgent need to understand the host response against viral infection. This virus targets distal lung cells and causes more severe disease than seasonal influenza virus, including diffuse alveolar damage and pulmonary edema. To define the mechanism of this tissue injury, it is important to study the specific cells that are infected by te virus. Therefore, our studies will focus on the cells in the alveolar region of the human lung. Our approach is novel in that we will study the effect of 2009 H1N1 pandemic virus on primary cultures of human alveolar epithelial cells and alveolar macrophages isolated from the same healthy lung donors. We have preliminary data using this system that suggests the involvement of both the AIM2 inflammasome and the cytokine TSLP in host response to influenza virus infection. The AIM2 inflammasome is important for host defense against bacteria and DNA virus infection, but a role for it in RNA virus infection has not previously been identified. Here we wil determine the function and mechanism of the AIM2 inflammasome in primary human ATII cells and in a mouse model during H1N1 influenza-induced epithelial injury. We hypothesize that AIM2 is the primary inflammasome induced by influenza virus in alveolar epithelial cells. AIM2 deficient cells and AIM2 deficient mice will have more impairment of the epithelial barrier during influenza infection. TSLP plays a key role in allergic diseases such as asthma, but its effect on the epithelial barrier is not yet defined. We will determine the role of TSLP in protecting the alveolar epithelial barrier during influenza infection using both in vitro and in vivo models. We hypothesize that inflammasome activation will enhance the TSLP production by alveolar epithelial cells. Influenza-stimulated TSLP will improve the damaged barrier by influenza both in vitro and in vivo through enhancing the tight junctions between cells and/or stimulating epithelial proliferation. In addition, the cell-cell interaction between alveolar epithelial cells and macrophages will enhance the release of TSLP by epithelial cells. Our study will reveal novel mechanisms for the regulation of the alveolar epithelial barrier during acute lung injury by influenza, thereby uncovering potential novel therapeutic strategies for reducing influenza-induced mortality.

描述（由申请人提供）：本项目旨在确定2009年H1N1流感病毒诱导的急性肺损伤中人类肺上皮细胞的稳态是如何调节的。由于H1N1大流行性病毒的快速传播和致病性增加的高潜力，迫切需要了解宿主对病毒感染的反应。这种病毒靶向远端肺细胞，引起比季节性流感病毒更严重的疾病，包括弥漫性肺泡损伤和肺水肿。为了确定这种组织损伤的机制，研究被te病毒感染的特定细胞是很重要的。因此，我们的研究将集中在人肺的肺泡区域中的细胞。我们 该方法是新颖的，因为我们将研究2009年H1N1大流行病毒对从相同健康肺供体分离的人肺泡上皮细胞和肺泡巨噬细胞的原代培养物的影响。我们使用该系统的初步数据表明，AIM 2炎性小体和细胞因子TSLP参与宿主对流感病毒感染的反应。AIM 2炎性小体对于宿主防御细菌和DNA病毒感染是重要的，但它在RNA病毒感染中的作用以前尚未确定。在这里，我们将确定AIM 2炎性体在原代人类ATII细胞和H1N1流感诱导的上皮损伤的小鼠模型中的功能和机制。我们推测AIM 2是流感病毒在肺泡上皮细胞中诱导的主要炎性小体。AIM 2缺陷型细胞和AIM 2缺陷型小鼠在流感感染期间将具有更多的上皮屏障损伤。TSLP在过敏性疾病如哮喘中起关键作用，但其对上皮屏障的作用尚未确定。我们将使用体外和体内模型确定TSLP在流感感染期间保护肺泡上皮屏障的作用。我们推测炎性小体的激活会增强肺泡上皮细胞产生TSLP。流感病毒刺激的TSLP可通过增强细胞间的紧密连接和/或刺激上皮细胞的增殖来改善流感病毒在体外和体内引起的屏障损伤。 增殖此外，肺泡上皮细胞与巨噬细胞之间的细胞-细胞相互作用将促进上皮细胞释放TSLP。我们的研究将揭示流感急性肺损伤期间肺泡上皮屏障调节的新机制，从而揭示降低流感诱导死亡率的潜在新治疗策略。