Pulmonary Blood Flow in Lung Development and Congenital Diaphragmatic Hernia

肺发育中的肺血流和先天性膈疝

• 批准号: 8327856
• 负责人: DOUGLAS A POTOKA
• 金额: $ 12.55万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-10 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8327856
• 关键词: Abdomen; Address; Advisory Committees; Affect; Area; Arteries; Award; Back; Basic Science; Biology; Blood Vessels; Blood flow; Cells; Chest; Childhood; Clinical; Complex; Congenital Abnormality; Congenital diaphragmatic hernia; Data; Defect; Dependence; Development; Development Plans; Developmental Biology; Distal; Embryo; Environment; Epithelial; Exhibits; Extracellular Matrix; Faculty; Fetal Development; Generations; Gestational Age; Goals; Infant; Infant Mortality; Injection of therapeutic agent; Institution; K-Series Research Career Programs; Knowledge; Lead; Life; Long-Term Survivors; Lung; Measures; Mentors; Mesenchymal; Mesenchyme; Modeling; Molecular; Molecular Genetics; Morbidity - disease rate; Morphogenesis; Mus; Organogenesis; Oxygen measurement, partial pressure, arterial; Patients; Pattern; Pediatric Surgical Procedures; Perfusion; Pericytes; Platelet-Derived Growth Factor; Play; Process; Pulmonary Hypertension; Recruitment Activity; Research; Research Personnel; Respiratory Diaphragm; Respiratory distress; Respiratory physiology; Role; Secondary to; Signal Pathway; Signal Transduction; Smooth Muscle Myocytes; Structure; Surgeon; Survivors; Techniques; Time; Translating; Trees; Tube; Ultrasonography; Viscera; Work; airway epithelium; angiogenesis; career development; design; effective therapy; experience; in utero; in vivo; lung development; meetings; mortality; neonate; nitrofen; novel; postnatal; precursor cell; prenatal; progenitor; research study; symposium; tissue oxygenation; vasculogenesis

DESCRIPTION (provided by applicant): This is an application for a K08 Career Development Award studying the role of embryonic pulmonary blood flow in normal lung development and the development of lung abnormalities seen in congenital diaphragmatic hernia (CDH). CDH is a birth defect occurring in approximately 1 out of 2,500 live-born infants. In CDH, there is a defect in the diaphragm allowing persistence of abdominal viscera in the chest cavity during fetal development. CDH is associated with varying degrees of lung hypoplasia, with decreased airway branching, and specific developmental defects of the pulmonary vasculature, including increased muscularization of intrapulmonary arteries. The combination of pulmonary hypertension, secondary to the underlying abnormal pulmonary vasculature, along with pulmonary hypoplasia results in often severe respiratory distress in neonates with CDH resulting in high infant mortality of up to 40%. Furthermore, a significant proportion of CDH survivors suffer from significant long-term morbidity. The potential role of embryonic pulmonary blood flow in modulating airway branching morphogenesis and pulmonary vascular development has not been examined. Also, the molecular mechanisms responsible for the development of pulmonary hypoplasia and pulmonary vascular abnormalities in CDH are incompletely understood. The overriding hypothesis for this proposal is that normal lung airway and vascular development is specifically dependent upon adequate embryonic pulmonary blood flow and that deficiencies in embryonic pulmonary blood flow contribute to lung developmental defects in CDH. To address this hypothesis, a novel technique of ultrasound-guided in utero embryonic mouse intracardiac injection utilizing a well-described murine model of CDH will be employed to pursue the following specific aims: 1) to demonstrate the dependence of airway branching morphogenesis on embryonic pulmonary blood flow in the developing lung; 2) to determine whether pulmonary arterial wall maturation is dependent upon embryonic pulmonary blood flow within the maturing vessel; and 3) to measure patterns of deficient embryonic pulmonary blood flow in CDH and determine whether defects in airway branching morphogenesis and vessel maturation in developing CDH lung are related to deficient embryonic pulmonary blood flow. Airway branching morphogenesis and pulmonary arterial wall maturation will be examined in relation to early embryonic pulmonary blood flow and tissue oxygenation in wide-type mice and in a murine model of CDH. The candidate is a pediatric surgeon who has been working closely with the mentor since becoming full-time faculty. The candidate benefits from a well-established and successful mentor and a very supportive research and practice environment. In addition, the candidate will have regular meetings with a scientific advisory committee compromised of experts in lung development and pulmonary vascular biology within the institution. The candidate's immediate goals are to obtain increased knowledge and proficiency in advanced experimental developmental biology concepts and techniques and to be able to design and conduct increasingly sophisticated experiments to address hypothesis-driven questions. The candidate's long-term goals are to become a productive independent investigator who is able to contribute significantly to the fields of developmental biology and pediatric surgery and eventually translate basic science findings back to the clinical realm. To achieve these goals a structured career development plan over the award period has been developed consisting of: gaining increased experience with advanced experimental techniques; course work; participation in conferences, symposia, and national meetings; frequent meetings with the mentor for guidance; and a gradual increase in independence over the award period.

描述（由申请人提供）：这是一份K 08职业发展奖的申请，研究胚胎肺血流在正常肺发育中的作用以及在先天性膈疝（CDH）中观察到的肺异常的发展。CDH是一种出生缺陷，大约每2，500名活产婴儿中就有1名发生。在先天性心脏病，有一个缺陷，在横膈膜允许持续存在的腹部内脏在胸腔中，在胎儿发育。CDH与不同程度的肺发育不全、气道分支减少和肺血管系统的特定发育缺陷（包括肺内动脉肌化增加）相关。继发于潜在的异常肺血管系统的肺动脉高压与肺发育不良的组合沿着导致患有CDH的新生儿经常严重呼吸窘迫，导致高达40%的高婴儿死亡率。此外，很大一部分CDH幸存者患有严重的长期发病率。胚胎肺血流在调节气道分支形态发生和肺血管发育中的潜在作用尚未研究。另外，CDH中肺发育不良和肺血管异常的分子机制还不完全清楚。这一建议的主要假设是，正常的肺气道和血管的发展是特别依赖于足够的胚胎肺血流和胚胎肺血流的不足，导致肺发育缺陷的CDH。为了解决这一假设，将采用超声引导的子宫内胚胎小鼠心内注射的新技术，该技术利用了良好描述的CDH小鼠模型，以实现以下特定目的：1）证明发育中的肺中气道分支形态发生对胚胎肺血流的依赖性; 2）确定肺动脉壁成熟是否依赖于成熟血管内的胚胎肺血流;和3）测量CDH中胚胎肺血流不足的模式，并确定发育中的CDH肺中气道分支形态发生和血管成熟的缺陷是否与胚胎肺血流不足有关。将在野生型小鼠和CDH小鼠模型中检查气道分支形态发生和肺动脉壁成熟与早期胚胎肺血流和组织氧合的关系。 候选人是一名儿科外科医生，自从成为全职教师以来一直与导师密切合作。候选人受益于一个成熟和成功的导师和一个非常支持的研究和实践环境。此外，候选人将定期与机构内肺发育和肺血管生物学专家组成的科学咨询委员会举行会议。候选人的直接目标是获得更多的知识和熟练掌握先进的实验发育生物学概念和技术，并能够设计和进行越来越复杂的实验，以解决假设驱动的问题。候选人的长期目标是成为一名富有成效的独立研究者，能够为发育生物学和儿科手术领域做出重大贡献，并最终将基础科学发现转化为临床领域。为了实现这些目标，在奖励期内制定了一个结构化的职业发展计划，包括：获得更多的经验，先进的实验技术;课程工作;参加会议，研讨会和国家会议;经常与导师会面指导;以及在奖励期内逐渐增加独立性。