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Role of dynamin for podocytes structure and function

动力对足细胞结构和功能的作用

基本信息

批准号：
8534113
负责人：
Sanja Sever
金额：
$ 35.64万
依托单位：
MASSACHUSETTS GENERAL HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-09-15 至 2016-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8534113
关键词：
Actins Adaptor Signaling Protein Affect Affinity Antibodies Applications Grants Arginine Binding C-terminal Clathrin Clathrin-Coated Vesicles Complex Cytoskeleton Data Down-Regulation Dynamin Endocytosis Epithelial Cells Fluorescence Microscopy Foot Process Functional disorder Gelsolin Glomerular Capillary Goals Guanosine Triphosphate Phosphohydrolases Higher Order Chromatin Structure In Vitro Integral Membrane Protein Intercellular Junctions Kidney Diseases Kidney Glomerulus Laboratories Link Lipids Mediating Membrane Microfilaments Molecular NCK adaptor protein 1 NPHS2 protein Phenotype Phosphorylation Play Proline Proteins Recruitment Activity Regulation Role SH3 Domains Signal Transduction Staging Structure Testing United States Work base blood filtration coated pit in vitro Assay mutant nephrin neuronal cell body novel podocyte polymerization slit diaphragm small molecule

项目摘要

DESCRIPTION (provided by applicant): The goal of this proposal is to elucidate the molecular mechanism(s) that underlie pathophysiology of proteinuric kidney diseases. Work from this laboratory recently demonstrated direct regulation of actin assembly in vitro and in podocytes by dynamin, and suggested an intricate interplay between dynamin's oligomerization cycle and actin cytoskeleton dynamics. Our findings motivate the hypothesis that signaling at the slit diaphragm alters dynamin oligomerization cycle through direct dynamin-Nck interactions, which in turn initiates actin polymerization in the membrane vicinity. In Specific Aim 1 we test whether clustering of Nck on the membrane promotes dynamin oligomerization into rings, which in turn drives actin polymerization in cultured podocytes. Using small molecules that specifically promote or inhibit dynamin oligomerization, as well as our novel actin binding domain mutants of dynamin, we test whether dynamin oligomerization cycle and actin-binding interactions are essential and/or sufficient for Nck-dependent polymerization of cortical actin cytoskeleton. In Specific Aim 2 we test whether direct interactions between dynamin and Nck alter the dynamin oligomerization cycle and dynamin-dependent actin polymerization using in-vitro assays. In Specific Aim 3, using TIR-FM we test whether direct dynamin-actin interactions are essential for clathrin mediated endocytosis.

描述（由申请人提供）：本提案的目的是阐明蛋白尿肾病病理生理基础的分子机制。该实验室最近的工作证明了动力蛋白在体外和足细胞中直接调节肌动蛋白的组装，并表明动力蛋白的寡聚周期和肌动蛋白细胞骨架动力学之间存在复杂的相互作用。我们的发现激发了一种假设，即狭缝隔膜上的信号通过直接动力蛋白- nck相互作用改变动力蛋白寡聚化周期，而动力蛋白寡聚化周期反过来又启动膜附近的肌动蛋白聚合。在特异性目的1中，我们测试了Nck在膜上的聚集是否促进动力蛋白寡聚化成环，从而驱动培养足细胞中的肌动蛋白聚合。利用小分子特异性促进或抑制动力蛋白寡聚化，以及我们的新动力蛋白结合域突变体，我们测试了动力蛋白寡聚化周期和肌动蛋白结合相互作用对于nck依赖的皮质肌动蛋白细胞骨架聚合是否必要和/或充分。在特异性目标2中，我们测试了动力蛋白和Nck之间的直接相互作用是否会改变动力蛋白寡聚化周期和动力蛋白依赖的肌动蛋白聚合。在Specific Aim 3中，我们使用TIR-FM测试了动力蛋白-肌动蛋白的直接相互作用是否对网格蛋白介导的内吞作用至关重要。