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Modeling Nephrotic Syndrome in Drosophila Nephrocytes

果蝇肾细胞肾病综合征建模

基本信息

批准号：
10019519
负责人：
ZHE HAN
金额：
$ 34.76万
依托单位：
UNIVERSITY OF MARYLAND BALTIMORE
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-04-10 至 2023-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10019519
关键词：
Actins Affect Animal Model Autophagocytosis Autophagosome Biological Biological Models Biology Cell physiology Child Collaborations Communities Complement Cytoskeleton DNA Sequence Alteration DNA sequencing Data Defect Disease Disease model Drosophila genus Drug Screening Drug Targeting End stage renal failure FRAP1 gene Funding Gene Mutation Gene Silencing Genes Genetic Genomics Grant Human Kidney Kidney Diseases Label Methods Modeling Molecular Structure Mus Mutation Nephrotic Syndrome Pathogenesis Pathogenicity Pathway interactions Patients Pharmaceutical Preparations Phenotype Play Process Regulation Renal function Renal glomerular disease Reproducibility Research Role Series Signal Pathway Steroid-resistant idiopathic nephrotic syndrome Study models System Technology Testing Therapeutic Effect Time Transgenic Organisms Validation Variant Work Zebrafish base cohort cost disease mechanisms study drug testing effective therapy fly gene replacement genetic variant in vivo inhibitor/antagonist innovation kidney cell live cell imaging novel novel therapeutics podocyte rare genetic disorder screening small molecule targeted treatment tool young adult

项目摘要

PROJECT SUMMARY/ABSTRACT: Nephrotic syndrome (NS) is one of the most frequent causes of End-Stage Renal Disease (ESRD) in children and young adults, but effective treatment is lacking, particularly for Steroid-Resistant Nephrotic Syndrome (SRNS). Rapid advances in DNA sequencing technology have led to the identification of large numbers of genetic variants that are potential causal factors for SRNS. However, lack of in vivo functional data for these candidate SRNS genes and their variants make it difficult to validate their roles in causing the disease. An animal model that carry the exact mutation found in patients for disease mechanism studies and testing of potential targeted therapies is in great demand. We have established a low-cost, high-efficiency Drosophila model system to generate essential functional data for candidate NS genes and variants, and to expedite the identification of novel NS genes. This novel kidney disease model system exploits the remarkable molecular, structural and functional equivalencies of Drosophila nephrocytes and human podocytes. We studied 40 known NS genes in nephrocytes and found that 85% of these genes play conserved roles in kidney cells from flies to humans. We also discovered underlying disease mechanisms by generating personalized fly NS models in which endogenous fly genes were functionally replaced by human homologs carrying patient-derived mutations. We also developed drug testing platform using these fly NS models, and successfully reversed the renal phenotype using targeted therapy informed by disease mechanism. In this renew proposal, we will use the powerful genetic tools in Drosophila to identify new renal genes involved in autophagy and cytoskeleton regulation. We will identify new nephrocyte cytoskeleton markers and components. We will also develop new personalized Drosophila models for candidate NS genes and novel genetic variants for known NS genes, as well as using the fly models to test potential targeted therapies. Our studies will provide the kidney disease research community with a low-cost high-efficiency model system to functionally validate NS associated genes and genetic variants, to identify novel NS genes, and to develop mechanism-based targeted therapies.

项目总结/摘要：肾病综合征（NS）是儿童终末期肾病（ESRD）最常见的病因之一但缺乏有效的治疗，特别是对激素抵抗性肾病综合征（SRNS）。DNA测序技术的快速发展已经导致鉴定出大量的遗传变异是SRNS的潜在致病因素。然而，缺乏这些的体内功能数据，候选SRNS基因及其变体使得难以证实它们在引起疾病中的作用。一个携带在患者中发现的确切突变的动物模型，用于疾病机制研究和潜在的靶向疗法需求巨大。我们建立了一个低成本、高效率的果蝇模型系统，以生成候选NS基因和变体的基本功能数据，并加快新NS基因的鉴定。这种新的肾脏疾病模型系统利用了显着的分子，果蝇肾细胞和人类足细胞的结构和功能等效性。我们研究了40个已知的 NS基因，并发现这些基因中的85%在从苍蝇到人类我们还通过生成个性化的果蝇NS模型发现了潜在的疾病机制，其中内源性果蝇基因在功能上被携带患者源性突变。我们还利用这些苍蝇NS模型开发了药物测试平台，并成功地逆转了肾表型使用靶向治疗告知疾病机制。在这个更新的建议中，我们将使用在果蝇中鉴定参与自噬和细胞骨架的新肾脏基因的强大遗传工具调控我们将确定新的肾细胞骨架标记物和成分。我们还将开发新的候选NS基因和已知NS基因的新遗传变体的个性化果蝇模型，以及使用果蝇模型来测试潜在的靶向治疗。我们的研究将提供肾脏疾病一个低成本高效率的模型系统，以功能验证NS相关基因的研究社区和遗传变异，以确定新的NS基因，并开发基于机制的靶向治疗。