Retinal Epithelial Polarity and Cellular Patterning

视网膜上皮极性和细胞图案

• 批准号: 7281182
• 负责人: XIANGYUN WEI
• 金额: $ 31.59万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-30 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7281182
• 关键词: Affect; Affinity Chromatography; Architecture; Biochemical; Biological; Candidate Disease Gene; Cell Polarity; Cells; Complex; Cues; Data; Defect; Development; Disease; Embryo; Engineering; Ensure; Epithelial; Epithelial Cells; Epithelium; Eye; Fishes; Genes; Genetic; Invertebrates; Link; Methods; Molecular; Morphogenesis; Neural Retina; Numbers; Organ; Pattern; Pattern Formation; Play; Protein Binding Domain; Protein Isoforms; Proteins; Research; Research Personnel; Retina; Retinal; Retinal Degeneration; Role; Series; Set protein; Staging; Structure; Structure of retinal pigment epithelium; System; Tertiary Protein Structure; Testing; Tissues; Transgenic Organisms; Yeasts; Zebrafish; cell motility; interest; knock-down; loss of function; programs; protein protein interaction; relating to nervous system; yeast two hybrid system

DESCRIPTION (provided by applicant): Retinal engineering is likely to be the ultimate cure for blinding disorders caused by degeneration of retinal cells. A prerequisite for retinal engineering is understanding the mechanisms of cellular pattern formation in the vertebrate retina. Our long-term research interest is to define these mechanisms. Recent studies suggest that the polarity of the retinal epithelia plays an essential role in neural retinal pattern formation; but the mechanisms involved are largely unknown. We have shown that three zebrafish polarity genes (nok, Pard3, and zLinT) are required to establish the cellular architecture of the mature retina. These proteins all contain well-established protein-protein interaction domains. Our data suggest that zLin7 likely interacts with Nok and that Nok is required for the interactions between the neural retina and the juxtaposed retinal pigmented epithelium (RPE). Our central hypothesis is that Nok, Pard3, and zLin7 associate with other proteins in a developmentally regulated fashion to collectively establish and/or maintain the proper polarity of retinal epithelia and consequently ensure accurate interactions between the neural retina and RPE. These interactions likely enable the proper distribution of cell migration cues required for retinal pattern formation. The major aims of the research to be pursued in this project include: 1) Determine to what extent Nok's function in controlling cellular pattern formation in the neural retina requires Nok's activity in the RPE by making and analyzing transgenic embryos that display mosaic Nok expressions in the eye; 2) Determine whether Nok physically interacts with one or more isoforms of zLin7's and what protein domains are involved in the interaction; 3) Identify and characterize the proteins that interact with Nok, Pard3, and zLin7 complexes during retinal development by using affinity purification, yeast two-hybrid, and candidate genes approaches.

描述（由申请人提供）：视网膜工程很可能是最终治愈由视网膜细胞变性引起的致盲性疾病。视网膜工程的先决条件是了解脊椎动物视网膜中细胞图案形成的机制。我们的长期研究兴趣是确定这些机制。最近的研究表明，视网膜上皮细胞的极性在神经视网膜模式的形成中起着重要的作用，但所涉及的机制在很大程度上是未知的。我们已经证明，三个斑马鱼极性基因（nok，Pard 3和zLinT）是建立成熟视网膜的细胞结构所必需的。这些蛋白质都含有公认的蛋白质-蛋白质相互作用结构域。我们的数据表明zLin 7可能与Nok相互作用，并且Nok是神经视网膜和并列视网膜色素上皮（RPE）之间相互作用所需的。我们的中心假设是，Nok、Pard 3和zLin 7以发育调节的方式与其他蛋白质相关联，共同建立和/或维持视网膜上皮细胞的适当极性，从而确保神经视网膜和RPE之间的准确相互作用。这些相互作用可能使视网膜图案形成所需的细胞迁移线索的适当分布成为可能。本项目的主要研究目标包括：1）通过制备和分析在眼睛中显示嵌合型Nok表达的转基因胚胎，确定Nok在控制神经视网膜中细胞模式形成的功能在多大程度上需要Nok在RPE中的活性; 2）确定Nok是否与zLin 7的一种或多种同种型物理相互作用，以及什么蛋白质结构域参与相互作用; 3）通过亲和纯化、酵母双杂交和候选基因方法鉴定和表征在视网膜发育期间与Nok、Pard 3和zLin 7复合物相互作用的蛋白质。