The Role of C3a and C5a in BEA Induced Nephritis

C3a 和 C5a 在 BEA 诱发肾炎中的作用

• 批准号: 6648320
• 负责人: MICHAEL C BRAUN
• 金额: $ 12.54万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-08-21 至 2007-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6648320
• 关键词: B lymphocyte; T lymphocyte; anaphylatoxins; antigen presenting cell; complement receptor; cytokine; disease /disorder model; epithelium; immunopathology; laboratory mouse; leukocyte activation /transformation; molecular pathology; monocyte; nephritis; protein biosynthesis; protein structure function; receptor expression; renal tubule

DESCRIPTION (provided by applicant):Throughout his clinical fellowship in pediatric nephrology and his postdoctoral training in immunology the candidate's interests have been focused on the relationship of complement and host immune response. This proposal represents an excellent opportunity for the candidate to work in a well regarded research environment which will contribute immensely to the candidate's knowledge of complement biology as well as immunologic aspects of renal injury. This proposal is based on two distinct, but interrelated findings; first, that the receptors for the anaphylatoxins, C3a and C5a, are highly expressed in proximal tubular epithelium, and second thatC3a and C5a have the capacity to attenuate CD4+ Thl T-cell responses. Based on the hypothesis that C3a and C5a, acting directly on proximal tubular epithelial cells and on the adaptive immune response, promote renal injury, we propose to define the role of C3a and C5a in the murine 2-Bromoethylamine (BEA) nephritis model. Initially, we will characterize both the expression and function of the C3a and C5a receptors in primary murine proximal tubular epithelial cells. Second, immunologic responses with respect to antigen presenting cell and T-cell function, as well as T-cell dependent B-cell activation will be defined in C3a and C5a receptor deficient mice. Lastly, functional and histological differences between C3a and C5a receptor deficient mice and wildtype littermate controls will be defined in both the acute tubular necrosis phase and the chronic tubulointerstitial disease phase of BEA induced nephritis. In addition, mononuclear cells will be isolated from renal tissue, phenotyped, and functionally characterized by patterns of cytokine production both at the protein and mRNA levels. The candidate's and the sponsor's interests are in understanding the role of the anaphylatoxins in immune mediated pathogenesis. The efforts of the proposal will have direct application to human disease. At the completion of this Award, the candidate will be prepared to continue as a highly productive independent investigator in the area of renal immunopathogenesis

描述（由申请人提供）：在他的儿科肾脏学临床研究和免疫学博士后培训期间，候选人的兴趣一直集中在补体和宿主免疫反应的关系上。该提案为候选人提供了一个极好的机会，可以在一个受人尊敬的研究环境中工作，这将极大地促进候选人对补体生物学以及肾损伤免疫学方面的知识。这一建议基于两个截然不同但相互关联的发现；首先，过敏毒素受体C3a和C5a在近端小管上皮中高度表达，其次，C3a和C5a具有减弱CD4+ Thl t细胞反应的能力。基于C3a和C5a直接作用于近端小管上皮细胞和适应性免疫反应，促进肾损伤的假设，我们提出确定C3a和C5a在小鼠2-溴乙胺（BEA）肾炎模型中的作用。首先，我们将描述C3a和C5a受体在原代小鼠近端小管上皮细胞中的表达和功能。其次，在C3a和C5a受体缺陷小鼠中，抗原提呈细胞和t细胞功能以及t细胞依赖的b细胞激活方面的免疫应答将被定义。最后，在BEA引起肾炎的急性肾小管坏死期和慢性肾小管间质病期，将定义C3a和C5a受体缺陷小鼠与野生型同窝对照之间的功能和组织学差异。此外，单个核细胞将从肾组织中分离出来，在蛋白质和mRNA水平上通过细胞因子产生模式进行表型和功能表征。候选人和赞助者的兴趣在于了解过敏毒素在免疫介导的发病机制中的作用。该提案的努力将直接应用于人类疾病。在完成本奖项后，候选人将准备继续作为肾脏免疫发病机制领域的高效独立研究者