Effects of BMPRII Mutations in Pulmonary Hypertension

BMPRII 突变对肺动脉高压的影响

• 批准号: 6803060
• 负责人: David M RODMAN
• 金额: $ 49.64万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-09-19 至 2007-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6803060
• 关键词: biological signal transduction; bone morphogenetic proteins; cell growth regulation; cell proliferation; gel mobility shift assay; gene mutation; genetically modified animals; human tissue; immunocytochemistry; interleukin 6; laboratory mouse; macrophage; muscle function; phenotype; polymerase chain reaction; pulmonary hypertension; receptor expression; respiratory epithelium; statistics /biometry; vascular smooth muscle; western blottings

DESCRIPTION (provided by applicant): Primary pulmonary hypertension (PPH) is a potentially lethal disorder characterized by pulmonary vasoconstriction and vascular remodeling involving abnormal proliferation of fibroblasts, smooth muscle and endothelial cells. In the year 2000, mutations in the type 2 bone morphogenic protein receptor (BMPR2) were identified as the genetic basis for familial PPH and about 30% of sporadic PPH. BMP signaling had not previously been connected to pulmonary hypertension, and the mechanistic linkage is unknown. We hypothesize that in normal individuals the BMP pathway acts to down-regulate both inflammatory cytokine-mediated positive feedback loops and vascular smooth muscle cell proliferation. Insufficient BMP pathway activity in individuals with BMPR2 mutations leads to insufficient damping of these auto-regulatory loops, resulting in the PPH phenotype. We provide preliminary evidence in cell culture systems supporting this hypothesis and have constructed a unique series of transgenic mice to further test the hypothesis. These mice express a human dominant-negative BMPR2 (dnBMPR2) using the tetracycline gene switch system, allowing both spatial and temporal control of expression. We have successfully bred smooth muscle cell and epithelial cell specific dnBMPR2 expressing mice, and are constructing endothelial cell specific mice at this time. Using our in vitro and transgenic models we will test the following three specific aims: 1: Test the hypothesis that the BMP pathway is a negative modulator of the cytokine interleukin-6 (IL-6) in PA SMC, leading to reduced IL-6-mediated signaling and proliferation. 2: Test the hypothesis that loss of PA SMC BMPR2 function in SM22-dnBMPR2 transgenic mice leads to an exaggerated pulmonary hypertensive response in vivo. 3: Test the hypothesis that loss of BMPR2 function in lung cell types other than SMC also contributes to the development of pulmonary hypertension. Upon completion of our studies, we will have tested the hypothesis that the link between BMP signaling and pulmonary hypertension involves both regulation of the critical cytokine, IL-6, as well as modulation of smooth muscle cell proliferation. We will have also tested the role of four pulmonary cell types, smooth muscle, endothelium, airway epithelium and macrophages in the link between BMPR2 and pulmonary hypertension.

描述（由申请人提供）：原发性肺动脉高压（PPH）是一种潜在致死性疾病，其特征为肺血管收缩和血管重塑，涉及成纤维细胞、平滑肌和内皮细胞的异常增殖。在2000年，2型骨形态发生蛋白受体（BMPR 2）的突变被确定为家族性PPH和约30%的散发性PPH的遗传基础。BMP信号以前没有被连接到肺动脉高压，其机制联系是未知的。我们推测，在正常人中，BMP通路的作用是下调炎症性丝氨酸介导的正反馈回路和血管平滑肌细胞增殖。在BMPR 2突变的个体中，BMP通路活性不足导致这些自动调节环的阻尼不足，从而导致PPH表型。我们在细胞培养系统中提供了支持这一假设的初步证据，并构建了一系列独特的转基因小鼠来进一步验证这一假设。这些小鼠使用四环素基因开关系统表达人显性阴性BMPR 2（dnBMPR 2），允许表达的空间和时间控制。我们已经成功地培育了平滑肌细胞和上皮细胞特异性表达dnBMPR 2的小鼠，目前正在构建内皮细胞特异性小鼠。使用我们的体外和转基因模型，我们将测试以下三个具体的目标：1：测试的假设，BMP途径是一个负调制器的细胞因子白细胞介素-6（IL-6）在PA SMC，导致减少IL-6介导的信号传导和增殖。第二章：检验SM 22-dnBMPR 2转基因小鼠中PA SMC BMPR 2功能丧失导致体内肺动脉高压反应加剧的假设。3：检验BMPR 2功能在除SMC以外的肺细胞类型中的丧失也有助于肺动脉高压的发展的假设。在我们的研究完成后，我们将测试的假设，BMP信号和肺动脉高压之间的联系涉及的关键细胞因子，IL-6的调节，以及平滑肌细胞增殖的调制。我们还将测试四种肺细胞类型（平滑肌、内皮、气道上皮和巨噬细胞）在BMPR 2和肺动脉高压之间的联系中的作用。