Control of Epithelial Polarity

上皮极性的控制

基本信息

批准号：
8919878
负责人：
Keith E Mostov
金额：
$ 33.6万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
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：
2011-07-01 至 2017-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8919878
关键词：
3-Dimensional Abbreviations Adhesives Annexins Apical Basement membrane Binding Canis familiaris Cell Line Cell membrane Cells Cellular biology Charge Collagen Cyst Data Development Enzymes Epithelial Epithelial Cells Extracellular Matrix Face Gel Hepatocyte Growth Factor Image Ions Kidney Life Lipids MDCK cell Membrane Mesenchymal Microscopy Modeling Molecular Molecular Models Movement Nephrons Organ PH Domain PTEN gene Phosphatidylinositol 4,5-Diphosphate Phosphatidylinositols Phospholipase D Phosphoric Monoester Hydrolases Phosphotransferases Polycystic Kidney Diseases Polymeric Immunoglobulin Receptors Positioning Attribute Protein Isoforms Proteins RNA Interference Recruitment Activity Role Scaffolding Protein Signal Transduction Surface Testing Thin Layer Chromatography Tight Junctions Tube Work base cellular imaging inhibitor/antagonist innovation inorganic phosphate inositol 4,5-bisphosphate inositol 4-phosphate inositol-1,4,5-trisphosphate 5-phosphatase matrigel molecular modeling monolayer phosphatidylinositol 3,4,5-triphosphate podocalyxin prevent protein transport research study sialomucin sialomucins sodium-hydrogen exchanger regulatory factor src Homology Region 2 Domain

项目摘要

DESCRIPTION (provided by applicant): Many internal organs, such as the kidney, consist of hollow tubules and spheres lined by a layer of polarized epithelial cells. These cells have an apical plasma membrane domain facing the central lumen and a basolateral plasma membrane facing the underlying basement membrane. These two plasma membrane domains have completely different protein and lipid compositions, and trafficking of proteins and lipids to these distinct membrane surfaces is vital. We have found that the signaling lipid phosphatidyl inositol 3,4,5- trisphosphate (PIP3) is found only at the basolateral plasma membrane and is a key determinant of the identity and formation of this surface. In contrast phosphatidyl inositol 4,5-bisphosphate (PIP2) is concentrated at the apical plasma membrane, where it is a main determinant of this surface. We will test the hypothesis that PIP2 and PIP3 control the development of epithelial polarity, using live cell imaging. We will test the hypothesis that PIP3 is synthesized at the basolateral plasma membrane by a specific isoform(s) of phosphatidyl inositiol 3- kinase. We will test the respective roles of the lipid phosphatases PTEN and SHIP1/2 in preventing PIP3 from accumulating at the apical plasma membrane. We will test the hypothesis that gp135/podocalyxin and proteins with which it interacts are directly involved in formation of the apical surface. Gp135 is a negatively charged, transmembrane sialomucin, which binds via a PDZ motif at its C-terminus to the scaffolding protein NHERF1. We will mislocalize gp135 to the basolateral surface and see if NHERF1 and other proteins follow. Much of the PIP2 at the plasma membrane is synthesized by phosphatidyl inositol 4- phosphate 5-kinase (PI5K). The isoform PI5K1beta is found at the apical plasma membrane and interacts with NHERF1. We will test the involvement of PI5K1beta (as well as the alpha and gamma isoforms) in formation of the apical plasma membrane. We will also test if PTEN is recruited to the apical plasma membrane by its interaction with NHERF. Together, these experiments will help us understand the molecular mechanism of apical plasma membrane and lumen formation.

描述（由申请人提供）：许多内部器官，例如肾脏，由空心小管和球形组成，由一层偏振上皮细胞衬里。这些细胞具有面向中央腔的顶端质膜结构域，并且面向下面的基底膜的基底外侧质膜。这两个质膜结构域具有完全不同的蛋白质和脂质组成，并且将蛋白质和脂质运输到这些不同的膜表面至关重要。我们发现，仅在基底外侧质膜上发现信号脂质磷脂酰肌醇3,4,5-三磷酸（PIP3），并且是该表面身份和形成的关键决定因素。相反，磷脂酰肌醇4,5-双磷酸盐（PIP2）集中在顶端质膜上，在该质膜中，它是该表面的主要决定因素。我们将检验以下假设：PIP2和PIP3使用活细胞成像控制上皮极性的发展。我们将检验以下假设：PIP3是通过磷脂酰inositiol 3-激酶在基底外侧质膜上合成的。我们将测试脂质磷酸酶PTEN酶和Ship1/2在防止PIP3在顶端质膜上积聚的各自作用。我们将检验以下假设：GP135/Podocalyxin和与其相互作用的蛋白质直接参与了顶部表面的形成。 GP135是一种负电荷的跨膜唾液素，它通过其C末端的PDZ基序与脚手架蛋白NHERF1结合。我们将将GP135错误地定位到基底外侧表面，并查看NHERF1和其他蛋白质是否遵循。质膜上的大部分PIP2由磷脂酰肌醇4-磷酸5-激酶（PI5K）合成。同工型PI5K1BETA在顶端质膜上发现并与NHERF1相互作用。我们将测试PI5K1BETA（以及α和γ同工型）在顶端质膜形成中的参与。我们还将通过与NHERF的相互作用来测试PTEN是否被募集到顶端质膜。这些实验将共同帮助我们理解顶端质膜和管腔形成的分子机制。