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Dynamics of Epithelial Polarity Proteins and the Control of Tissue Architecture

上皮极性蛋白的动力学和组织结构的控制

基本信息

批准号：
8423865
负责人：
James Todd Blankenship
金额：
$ 2.63万
依托单位：
UNIVERSITY OF DENVER (COLORADO SEMINARY)
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：
2011-09-01 至 2016-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8423865
关键词：
Actomyosin Address Adhesions Apical Architecture Behavior Cell Adhesion Cell Polarity Cell membrane Cell surface Cell-Cell Adhesion Cells Cochlea Communities Complex Computational Technique Cytoskeleton Data Development Developmental Process Disease Drosophila genus E-Cadherin Embryo Environment Epithelial Epithelial Cells Epithelium Event Exocytosis F-Actin Funding Generations Genes Genetic Grant Green Algae Human Imaging Techniques Individual Intention Kinetics Life Maintenance Malignant Neoplasms Mediator of activation protein Membrane Membrane Protein Traffic Movement Mutation Neoplasm Metastasis Optics Organ Organism Palate Pathway interactions Positioning Attribute Process Property Proteins Reagent Research Role Screening procedure Shapes Site Skin Structure Techniques Tertiary Protein Structure Testing Tissues Vesicle Work aqueous intercalation molecular dynamics mutant new growth novel programs rab11 protein tissue repair tool trafficking

项目摘要

DESCRIPTION (provided by applicant): Dynamics of Epithelial Polarity Proteins and the Control of Tissue Architecture Epithelial sheets sit at the boundary of the organism and its external environment. The maintenance of these apical and basolateral domains is essential to the barrier function of epithelia, and the loss of apical-basal polarity is associated with the metastasis of many epithelial cancers. While epithelial sheets were once viewed as largely static assemblies, it is now appreciated that these are dynamic structures that can undergo significant reorganizing and renewal events. Indeed, cell neighbor exchange can be harnessed by developmental processes to effect changes in tissue architecture, and cell intercalation can drive epithelial tissue repair. In the Drosophila embryonic epithelium, individual cells are able to either consolidate cell-cell contacts or direct neighbor exchange movements through the asymmetric localization of cell adhesion and polarity proteins. While it is now apparent that actomyosin contraction drives the shrinking and loss of cell-cell interfaces, the means by which epithelial cells create new cell contacts and interfaces is unknown. The main question addressed in this project is the identification of the mechanism by which new cellular interfaces are established and maintained. We hypothesize that an early and essential event in the creation of the new interfaces that drive neighbor exchange will be directed membrane addition. The role of a key mediator of new membrane addition, the exocyst complex, in directing localized vesicular trafficking during tissue elongation will be characterized. We will also generate novel tools by drawing on recently created optical highlighter proteins that will allow the dynamic tracking of specific subpopulations of adhesion proteins. These tools and techniques should be useful to the general Drosophila community. Finally, genetic approaches are underway to identify new components involved in the establishment of distinct properties of cell polarity. The approaches used in these studies will draw on advanced imaging techniques that are just beginning to be applied to Drosophila. The funding of this project will be the first major grant for the newly established lab and will represent an important step towards the founding of an independent research program.

描述(申请人提供)：上皮极性蛋白的动力学和组织结构的控制上皮片位于生物体及其外部环境的边界。这些顶端和基底外侧结构域的维持对上皮细胞的屏障功能至关重要，而顶端-基底端极性的丧失与许多上皮癌的转移有关。虽然上皮片曾经被认为主要是静态的组装，但现在人们意识到，这些是动态的结构，可以经历重大的重组和更新事件。事实上，细胞邻接交换可以被发育过程利用来影响组织结构的变化，而细胞嵌入可以驱动上皮组织修复。在果蝇胚胎上皮中，单个细胞能够通过细胞黏附和极性蛋白的不对称定位来巩固细胞与细胞之间的接触或直接邻近交换运动。虽然现在很明显，肌动球蛋白收缩导致细胞-细胞界面的收缩和丧失，但上皮细胞建立新的细胞接触和界面的方式尚不清楚。本项目涉及的主要问题是确定建立和维护新的蜂窝接口的机制。我们假设，在驱动邻居交换的新界面的创建中，一个早期和基本的事件将是定向的膜加成。一个新的膜添加的关键媒介，外囊复合体，在引导局部囊泡在组织伸长过程中的运输中的作用将被表征。我们还将通过利用最近创建的光学荧光蛋白来生成新的工具，这些蛋白将允许动态跟踪黏附蛋白的特定亚群。这些工具和技术应该对一般的果蝇社区有用。最后，目前正在采用遗传学方法来确定与确定细胞极性的不同属性有关的新成分。这些研究中使用的方法将借鉴先进的成像技术，这些技术刚刚开始应用于果蝇。该项目的资金将是为新成立的实验室提供的第一笔重大赠款，并将代表着朝着建立独立研究计划迈出的重要一步。