Understanding cell biology of Delta-Notch interactions

了解 Delta-Notch 相互作用的细胞生物学

• 批准号: 7015089
• 负责人: GERALDINE A WEINMASTER
• 金额: $ 24.04万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-02-15 至 2008-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7015089
• 关键词: biological signal transduction; cell cell interaction; cell line; cell surface receptors; confocal scanning microscopy; developmental genetics; developmental neurobiology; dynamin; flow cytometry; gene expression; ionophores; ligase; membrane proteins; mixed tissue /cell culture; molecular pathology; multiinfarct dementia; neuropathology; protein localization; proteolysis; receptor binding; receptor mediated endocytosis; stroke; ubiquitin

DESCRIPTION (provided by applicant): Notch signaling regulates a wide variety of mammalian cell fates and processes. The Notch signaling pathway is activated through direct cell-cell interactions that facilitate binding between the transmembrane ligand Delta on a signaling cell and the Notch receptor on a responding cell. Activation of this signaling pathway relies on Delta to induce Notch proteolysis for release of the biologically active Notch intracellular domain (NICD) that regulates expression of Notch target genes. Although the generation and activity of NICD has been intensively studied, little is known regarding the role and fate of the Notch extracellular domain (NECD) generated during Delta-induced Notch signaling. Studies have indicated that NECD removal is necessary for Notch proteolysis to occur; however, the mechanism of NECD release is not well defined. It has been proposed that NECD is released by ADAM shedding, but direct demonstration of ligand-induced NECD shedding has not been reported. Alternatively, NECD has been proposed to be removed through internalization into Delta cells, through a poorly characterized process of trans-endocytosis. However, evidence for transfer of NECD into Delta cells has so far only been obtained for Drosophila cells. The major aim of this proposal is to develop a system that will allow us to image and characterize transfer of NECD to interacting Delta cells using a mammalian cell co-culture assay. For these studies, we will use a combination of fluorophore-conjugated antibodies and tagged forms of Delta and Notch to localize transfer of Notch to co-cultured Delta cells using confocal microscopy. Given that the Notch extracellular domain accumulates in brains of CADASIL patients, understanding the fate of NECD is relevant to this inherited vascular dementia. Any information gained regarding the fate and role of the NECD during Notch signaling is expected to have biological and health related significance for understanding the molecular basis of stroke and dementia in CADASIL. Consistent with the NINDS Exploratory/Developmental Grant (R21) Program, experiments are proposed to initiate studies on the role of endocytosis in Delta induced Notch signaling to provide requisite data for longer-term, program specific funding (R01).

描述(申请人提供)：Noch信号调节多种哺乳动物细胞的命运和过程。Notch信号通路是通过直接的细胞-细胞相互作用来激活的，这种相互作用促进了信号细胞上的跨膜配体Delta与反应细胞上的Notch受体之间的结合。这一信号通路的激活依赖于Delta诱导Notch蛋白降解，从而释放具有生物活性的Notch胞内域(NICD)，NICD调节Notch靶基因的表达。虽然NICD的产生和活性已经得到了广泛的研究，但关于在Delta诱导的Notch信号转导过程中产生的Notch胞外区(NECD)的作用和命运还知之甚少。研究表明，NECD的去除是Notch蛋白降解所必需的；然而，NECD的释放机制尚未很好地确定。有人提出NECD是由Adam Shedding释放的，但还没有直接证明配体诱导的NECD脱落的报道。或者，NECD已被提议通过内化到Delta细胞，通过一个特征不佳的跨内吞过程来去除。然而，到目前为止，仅在果蝇细胞中获得了NECD转移到Delta细胞的证据。这项建议的主要目的是开发一种系统，使我们能够使用哺乳动物细胞共培养试验来成像和表征NECD向相互作用的Delta细胞的转移。在这些研究中，我们将使用荧光团结合的抗体和标记形式的Delta和Notch来利用共聚焦显微镜定位Notch的转移到共培养的Delta细胞。鉴于Notch细胞外域在CADASIL患者的大脑中积累，了解NECD的命运与这种遗传性血管性痴呆有关。任何关于NeCD在Notch信号转导过程中的命运和作用的信息都有望对理解CADASIL中中风和痴呆的分子基础具有生物学和健康相关的意义。与NINDS探索性/发育资助(R21)计划一致，我们建议开展实验，研究内吞作用在Delta诱导的Notch信号中的作用，为长期的、计划特定的资助(R01)提供必要的数据。