Mitotic Rounding and Planar Spindle Alignment in Proliferating Epithelia

增殖上皮细胞中的有丝分裂圆整和平面纺锤体排列

基本信息

批准号：
9119141
负责人：
MATTHEW C GIBSON
金额：
$ 29.04万
依托单位：
STOWERS INSTITUTE FOR MEDICAL RESEARCH
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-08-01 至 2020-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9119141
关键词：
Abnormal Cell Actins Address Adopted Animal Model Animals Apical Architecture Area Biochemical Biological Assay Biology Carcinoma Cell Polarity Cell Proliferation Cell division Cell physiology Cells Cellular biology Complex Data Defect Development Disease Disseminated Malignant Neoplasm Drosophila genus Early Diagnosis Early treatment Elements Epithelial Epithelial Cell Proliferation Epithelial Cells Epithelium Event Experimental Models Foundations Genetic Genetic Models Health Homeostasis Human Image Intercellular Junctions Interphase Knowledge Lead Life Maintenance Malignant Neoplasms Mammals Mesenchyme Metaphase Mitosis Mitotic Mitotic spindle Modeling Molecular Molecular Genetics Morphogenesis Morphology Myosin ATPase Organ Pathogenesis Pathologic Processes Pathology Pathway interactions Physiology Process Proliferating Prophase Proteins Proteomics Rho-associated kinase Role Site Structure Surface System Testing Tissues Tumor Suppressor Proteins base epithelial to mesenchymal transition genetic analysis genetic profiling human disease imaginal disc imaging modality in vivo in vivo Model innovation insight moesin monolayer neoplastic novel polarized cell research study src Homology Region 2 Domain tumor

项目摘要

DESCRIPTION (provided by applicant): Mitotic Rounding and Planar Spindle Alignment in Proliferating Epithelia Project Summary During development and homeostasis of multicellular animals, adherent layers of proliferating epithelial cells provide the spatial and structural contet essential for nearly all aspects of organ morphogenesis and physiology. In humans, defects in the control of epithelial cell proliferation can result in a wide range of pathologies, including te approximate 80% of cancers derived from epithelia (carcinomas). Nevertheless, despite the central importance of understanding epithelial proliferation in development and disease, precisely how mitotic division is spatially and temporally coordinated with the maintenance of epithelial architecture remains poorly understood. In this proposal, we take advantage of Drosophila imaginal discs as a genetic model to uncover fundamental molecular and cellular mechanisms that coordinate cell proliferation with epithelial apico-basal polarization in vivo. In Aim 1 we use genetic analysis and innovative live imaging methods to investigate how mitotic epithelial cells disassemble their complex interphase morphologies at prophase entry and subsequently round up at the apical epithelial surface. In Aim 2 we use genetic, biochemical, and proteomic approaches to interrogate interactions between the mitotic spindle poles and the junction-localized tumor suppressors Scribble and Discs Large during planar spindle alignment in vivo. Lastly, in Aim 3 we investigate the molecular and cellular features of epithelial-to-mesenchymal transitions (EMTs) that result from defective planar orientation of the mitotic spindle during epithelial cell division. At the conclusion of these studies, we will have greatly expanded our fundamental knowledge of epithelial cell division and planar spindle orientation developed a novel genetically-tractable model for abnormal EMT events that result from defective spindle orientation in vivo, and provided detailed mechanistic insight into the molecular genetic control of both of these processes.

描述（由申请人提供）：增殖上皮细胞中的有丝分裂圆形和平面纺锤体排列项目摘要在多细胞动物的发育和稳态过程中，增殖上皮细胞的粘附层提供了器官形态发生和生理学的几乎所有方面所必需的空间和结构内容。对人类来说，上皮细胞增殖控制缺陷会导致多种病理，包括大约 80% 的癌症源自然而，尽管了解上皮增殖在发育和疾病中的核心重要性，但有丝分裂如何在空间和时间上与上皮结构的维持相协调仍然知之甚少。作为遗传模型来揭示协调细胞增殖与体内上皮顶端基底极化的基本分子和细胞机制。在目标 1 中，我们使用遗传分析和创新的实时成像方法进行研究。有丝分裂上皮细胞如何在前期进入时分解其复杂的间期形态，并随后在顶端上皮表面聚集。在目标 2 中，我们使用遗传、生化和蛋白质组学方法来探究有丝分裂纺锤体极与连接处肿瘤抑制因子之间的相互作用。最后，在目标 3 中，我们研究了体内平面纺锤体排列过程中的大圆盘和大圆盘的分子和细胞特征。上皮细胞向间充质转化（EMT）是由于上皮细胞分裂过程中有丝分裂纺锤体平面方向缺陷引起的。这些研究的结论是，我们将极大地扩展我们对上皮细胞分裂和平面纺锤体方向的基础知识，并开发出一种新的方法。体内纺锤体方向缺陷导致异常 EMT 事件的遗传可处理模型，并提供了分子机制的详细见解这两个过程的遗传控制。