权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Hedgehog-mediated regulation of cell adhesion

Hedgehog 介导的细胞粘附调节

基本信息

批准号：
8795099
负责人：
Xiaoyan Zheng
金额：
$ 24.28万
依托单位：
GEORGE WASHINGTON UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2013
资助国家：
美国
起止时间：
2013-01-01 至 2016-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8795099
关键词：
Adhesions Adhesiveness Adhesives Affect Affinity Animals Anterior Binding Biochemical Biological Brothers Cell Adhesion Cell Adhesion Molecules Cell Aggregation Cell Separation Cell surface Cells Cultured Cells Development Drosophila genus Enhancers Erinaceidae Fibronectins Genes Genetic Genetic Models Genetic Screening Goals Growth Homologous Gene Human Immunoglobulins Lead Light Malignant - descriptor Malignant Neoplasms Mediating Methods Molecular Molecular Profiling Neoplasm Metastasis Oncogenes Pattern Population Positioning Attribute Process Property Protein Family Proteins Refractory Regulation Shapes Signal Transduction System Techniques Time Tissues To specify Wing base cancer cell gain of function genetic approach imaginal disc in vivo morphogens new therapeutic target paracrine promoter receptor receptor internalization research study response segregation smoothened signaling pathway tumor growth tumor progression

项目摘要

Tissue patterning in animal development requires adhesive mechanisms that promote and maintain physical segregation of different cell populations. Many paracrine morphogen signals have been proposed to specify the differences in cell affinity and the formation of sharp and stable boundaries which, in turn, serve to maintain the position and shape of morphogen organizers during the growth of a tissue. The long-term goal of this project is to understand the cellular and molecular mechanisms by which the Hedgehog (Hh) signal defines specific cell affinities and lead to the segregation of Hh-secreting (non-responding) cells and Hh-responding (non-secreting) cells. Increasing evidence indicates that Hh secreted by certain human cancer cells may signal to surrounding tissue and promote tumor growth and metastasis. Furthermore, malignant invasion might be considered a normal process of cell segregation in reverse, in which there is cross-adhesion between cancer cells and tissue cells. Therefore, this study will not only contribute significantly to our knowledge of the molecular and cellular bases of tissue patterning and further understanding of the Hh signal pathway, per se, but will also shed light on the mechanisms of cancer progression, perhaps leading to the discovery of new therapeutic targets in cancers. The Drosophila wing imaginal disc is subdivided into an anterior (A) and a posterior (P) compartment. P cells secrete Hh and, at the same time, are refractory to the Hh signal. In contrast, A cells can receive and respond to Hh, but do not express Hh by themselves. The cells of the two compartments do not intermingle during development. However, A cells unable to respond to the Hh signal no longer segregate from P cells. The current view is that the response to the Hh signal induces a change in the adhesiveness and that this difference leads to the segregation of A cells from P cell. Combining this model genetic system with broad experimental approaches that incorporate powerful biochemical, molecular and cellular techniques, I propose: 1) To investigate how the Hh signal directly alters the affinity differences between Hh-secreting P cells and Hh- responding A cells by modulating cell surface levels of the Ihog family proteins. 2) To identify additional cell adhesion molecules involved in regulating A/P cell segregation. 3) To investigate whether and how the Shh signal alters cell affinity by regulating expression levels of the vertebrate Ihog homologues.

动物发育中的组织图案化需要促进和维持不同细胞群体的物理隔离。许多旁分泌形态原信号已被提出具体说明细胞亲和力的差异以及尖锐而稳定的边界的形成，这反过来又有助于在组织生长过程中保持形态组织者的位置和形状。的长期目标是这个项目是为了了解Hedgehog(HH)信号定义的细胞和分子机制特定的细胞亲和力并导致HH分泌(无反应)细胞和HH反应细胞的分离 (不分泌)细胞。越来越多的证据表明，某些人类癌细胞分泌的HH可能发出信号并促进肿瘤的生长和转移。此外，恶性侵袭可能是被认为是一种正常的细胞分离过程，在这种过程中，癌细胞之间存在交叉粘连细胞和组织细胞。因此，这项研究不仅将大大有助于我们对组织构型的分子和细胞基础以及对HH信号通路的进一步了解，本身，但也将阐明癌症进展的机制，可能导致新的发现癌症的治疗靶点。果蝇翅膀形象盘分为前(A)室和后(P)室。P 细胞分泌HH，同时对HH信号不敏感。相比之下，A细胞可以接收和回答HH，但不要自己表达HH。两个隔间的单元格不混合。在开发过程中。然而，不能响应HH信号的A细胞不再与P细胞分离。目前的观点是，对HH信号的响应导致了粘附性的变化，这差异导致A细胞和P细胞的分离。将该模型遗传系统与BREADS相结合融合了强大的生物化学、分子和细胞技术的实验方法，我建议： 1)研究HH信号如何直接改变HH分泌的P细胞和HH-1细胞之间的亲和力差异。通过调节Ihog家族蛋白的细胞表面水平来响应A细胞。2)识别附加单元参与调节A/P细胞分离的黏附分子。3)调查Shh是否以及如何信号通过调节脊椎动物Ihog同源物的表达水平来改变细胞亲和力。