MAST CELL CYSTEINE PROTEASES IN LUNG INFLAMMATION

肺部炎症中的肥大细胞半胱氨酸蛋白酶

• 批准号: 6388547
• 负责人: Paul j WOLTERS
• 金额: $ 12.18万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-08-04 至 2004-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6388547
• 关键词: cysteine endopeptidases; enzyme structure; genetically modified animals; inflammation; laboratory mouse; lung disorder; mast cell; protein purification; protein structure function

Mast cell cysteine, metalloprotease, and serine proteases may play a significant role in the pathogenesis of inflammatory lung diseases. The long-term objective of this proposal is to identify the cysteine proteases present in mast cells, and to characterize their roles in mast cell dependent inflammation. We hypothesize that tissue mast cells are a major source of dipeptidyl peptidase I (DPPI) and a newly identified 60-kDa cysteine protease and that these proteases participate in inflammation by hydrolyzing extracellular proteins. Specific aims are : 1. To explore structure-function relationships of DPPI; 2. To identify cells expressing DPPI in normal and inflamed lung tissues; 3. To characterize substrate specificity of DPPI, and 4. To characterize a nove1 60 kDa cysteine protease found in mast cells. To achieve these goals: 1. Proteolytic processing of proDPPI will be studied in recombinantly expressed DPPI. 2. DPPI's expressed with mutated propeptides will be assayed for their dipeptidyl peptidase and endoprotease activity, 3. Expression of DPPI by specific cell types in normal and inflamed dog lungs will be determined by immunohistochemistry and in situ hybridization. 4. DPPI will be studied for its ability to hydrolyze extracellular peptides and proteins. 5. Mast cell functional characteristics and proteolytic activities will be studied in DPPI knockout mice. 6. A novel mast cell cysteine protease will be purified and characterized. Dr. Wolters has completed training in internal medicine and pulmonary and critical care medicine. He has demonstrated a firm commitment to a career in academic medicine and an interest in studying the pathophysiology of lung diseases. The research training plan includes: an intensive laboratory experience, didactic coursework, weekly seminars, and journal clubs. The research training will be overseen by an advisory committee including the sponsor (Dr. Caughey) and experts on cysteine proteases (Dr. McKerrow), immunohistopathology (Dr. McDonald), and pulmonary diseases (Dr. Matthay), who will guide the candidates development into an independent investigator in pulmonary research.

肥大细胞半胱氨酸、金属蛋白酶和丝氨酸蛋白酶可能在炎症性肺疾病的发病机制中起重要作用。 该提案的长期目标是鉴定肥大细胞中存在的半胱氨酸蛋白酶，并表征其在肥大细胞依赖性炎症中的作用。 我们假设组织肥大细胞是二肽基肽酶I（DPPI）和一种新鉴定的60 kDa半胱氨酸蛋白酶的主要来源，这些蛋白酶通过水解细胞外蛋白参与炎症。 具体目标是：1。探讨DPPI的结构与功能关系; 2.鉴定正常和炎症肺组织中表达DPPI的细胞; 3.表征DPPI的底物特异性，和4.目的：鉴定肥大细胞中一种新的60 kDa半胱氨酸蛋白酶。 为了实现这些目标：1。将在重组表达的DPPI中研究proDPPI的蛋白水解加工。 2.用突变的前肽表达的DPPI将测定其二肽基肽酶和内切蛋白酶活性，3.将通过免疫组织化学和原位杂交测定正常和炎症犬肺中特定细胞类型的DPPI表达。 4.将研究DPPI水解细胞外肽和蛋白质的能力。 5.将在DPPI敲除小鼠中研究肥大细胞功能特征和蛋白水解活性。 6.一种新的肥大细胞半胱氨酸蛋白酶将被纯化和表征。沃尔特斯博士已经完成了内科、肺病和重症监护医学的培训。 他表现出坚定的承诺，在学术医学的职业生涯和研究肺部疾病的病理生理学的兴趣。 研究培训计划包括：密集的实验室经验，教学课程，每周研讨会和期刊俱乐部。 研究培训将由一个咨询委员会监督，该委员会包括申办者（Caughey博士）和半胱氨酸蛋白酶（McKerrow博士）、免疫组织病理学（McDonald博士）和肺部疾病（Matthay博士）专家，他们将指导候选人发展成为肺部研究的独立研究者。