Mesenchymal stromal cell matricellular protein expression and bronchopulmonary dy

间充质基质细胞基质细胞蛋白表达与支气管肺疾病

• 批准号: 8165200
• 负责人: Antonia Petrova Popova
• 金额: $ 14.78万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-12 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8165200
• 关键词: Actins; Alveolar; Alveolus; Area; Aspirate substance; Bioinformatics; Biological Markers; Biology; Bronchopulmonary Dysplasia; Cell Proliferation; Cells; Childhood; Childhood Asthma; Chronic lung disease; Clinical; Clinical Investigator; Clinical Research; Collagen; Confidence Intervals; Coupled; Data; Deposition; Development; Disease; Doctor of Medicine; Dysplasia; Enrollment; Enzyme-Linked Immunosorbent Assay; Experimental Designs; Extracellular Matrix Proteins; Fellowship; Fiber; Fibroblast Growth Factor; Fibrosis; Gene Expression; Genes; Goals; Growth Factor Overexpression; Health; Immunoblotting; Incidence; Infant; Informed Consent; Lasers; Lung; Measures; Medicine; Mentors; Mentorship; Mesenchymal; Messenger RNA; Methods; Michigan; Microscopy; Modeling; Mus; Myofibroblast; NADPH Oxidase; Neonatal; Odds Ratio; Outcome; Paper; Pathogenesis; Patients; Phenotype; Pilot Projects; Plasminogen Activator; Play; Premature Infant; Proteins; Public Health Schools; Publishing; Pulmonology; Regression Analysis; Research; Research Personnel; Role; Sampling; Signal Transduction; Smooth Muscle Actin Staining Method; Stromal Cells; Supervision; Testing; Training; Training Programs; Transforming Growth Factors; Translating; Universities; Vascular Endothelial Cell; Work; base; biobank; career; connective tissue growth factor; experience; human tissue; improved; inhibitor/antagonist; insight; lung injury; mRNA Expression; overexpression; patient oriented research; periostin; programs; protein expression; receptor binding; response; skills; statistics

DESCRIPTION (provided by applicant): Antonia P. Popova, M.D., a pediatric pulmonologist, is focusing her career on bronchopulmonary dysplasia (BPD), a chronic lung disease of prematurely-born infants. During her fellowship, Dr. Popova published 4 papers on BPD and lung mesenchymal stromal cells. During the proposed training, Dr. Popova will continue work with her Mentor, Marc Hershenson, and receive additional scientific direction from Co-Mentor Stephen Weiss, an expert in matrix biology. However, her main goal will to be to acquire skills needed to become an independent investigator in the conduct of patient-oriented research, and to translate basic discoveries to the clinical problem of BPD. To achieve this, Dr. Popova will enroll in the School of Public Health Clinical Research Masters Program and receive additional mentorship from Dr. Fernando Martinez, an established pulmonary clinical investigator. She will also take coursework in computational medicine and bioinformatics under the supervision of a third Co-Mentor, Dr. Santiago Schnell. Dr. Popova's general hypothesis is that mesenchymal stromal cell myofibroblastic differentiation and matricellular protein expression play critical roles in BPD pathogenesis. To test this, she proposes the three Specific Aims, each of which is paired with Specific Training Objectives: 1. Measure the gene expression of lung mesenchymal stromal cells, focusing on matricellular proteins. Specific hypothesis: Mesenchymal stromal cells maintain a stable phenotype of myofibroblastic differentiation that is coupled with matricellular protein expression. Tracheal aspirates of premature infants will be examined for matricellular protein expression and mesenchymal stromal cells. Stromal cell mRNA and protein expression will be measured by microarray and ELISA/immunoblotting. Training Objective: Develop experience and understanding in experimental design, informed consent, and management of a research team. 2. Correlate neonatal lung mesenchymal stromal cell matricellular protein expression with clinical outcomes. Specific hypothesis: Expression of the matricellular proteins predicts BPD development. Relative odds of BPD as a function of tracheal aspirate protein expression and mesenchymal stromal cell gene expression will be calculated using multivariate regression analysis. Training Objectives: Acquire experience and understanding in the areas of experimental design, statistics, computational medicine and bioinformatics. 3. Examine expression and localization of matricellular proteins in the lungs of premature infants. Specific hypothesis: Matricellular protein expression is increased in the lungs of infants with BPD. Using University of Rochester neonatal lung biorepository samples, matricellular protein expression will be assessed by laser capture microscopy, qPCR and stereology-based quantitative immunohistochemisty. Training Objective: Acquire experience/expertise in methods used to quantify gene expression in small samples of human tissue. Completion of this work will provide insight into the origins of BPD and provide training for Dr. Popova, facilitating her transition to independent investigator in patient-oriented research.

描述（由申请人提供）：Antonia P.波波娃，医学博士，一位儿科肺病学家，正专注于支气管肺发育不良（BPD），一种早产儿的慢性肺病。在研究期间，波波娃博士发表了4篇关于BPD和肺间充质基质细胞的论文。在拟议的培训期间，波波娃博士将继续与她的导师马克·赫申森合作，并接受共同导师斯蒂芬·韦斯（基质生物学专家）的额外科学指导。然而，她的主要目标将是获得所需的技能，成为一个独立的研究人员在以病人为导向的研究行为，并将基本发现转化为BPD的临床问题。为了实现这一目标，波波娃博士将参加公共卫生学院的临床研究硕士课程，并接受费尔南多马丁内斯博士，一个既定的肺部临床研究员额外的指导。她还将在第三位共同导师圣地亚哥施内尔博士的监督下学习计算医学和生物信息学课程。波波娃博士的一般假设是间充质基质细胞成肌纤维细胞分化和基质细胞蛋白表达在BPD发病机制中起关键作用。为了验证这一点，她提出了三个具体目标，每一个都与具体的培训目标配对：1。测量肺间充质基质细胞的基因表达，重点是基质细胞蛋白。具体假设：间充质基质细胞保持稳定的成肌纤维细胞分化表型，其与基质细胞蛋白表达偶联。早产儿的气管吸出物将检查基质细胞蛋白表达和间充质基质细胞。将通过微阵列和ELISA/免疫印迹法测量基质细胞mRNA和蛋白质表达。培训目标：培养实验设计、知情同意和研究团队管理方面的经验和理解。 2.新生儿肺间充质基质细胞基质细胞蛋白表达与临床预后的相关性。具体假设：基质细胞蛋白的表达预测BPD的发展。将使用多变量回归分析计算作为气管抽吸物蛋白表达和间充质基质细胞基因表达的函数的BPD的相对几率。培训目标：在实验设计，统计学，计算医学和生物信息学领域获得经验和理解。 3.检测早产儿肺中基质细胞蛋白的表达和定位。特定假设：BPD婴儿肺部的基质细胞蛋白表达增加。使用罗切斯特大学新生儿肺生物储存库样本，通过激光捕获显微镜、qPCR和基于体视学的定量荧光化学评估基质细胞蛋白表达。培训目标：获得用于定量小样本人体组织中基因表达的方法的经验/专业知识。 这项工作的完成将使人们深入了解BPD的起源，并为波波娃博士提供培训，促进她过渡到以患者为导向的研究的独立研究者。