TUMOR CELL DESTRUCTION--PATH FROM BINDING TO LYSIS

肿瘤细胞破坏——从结合到裂解的路径

• 批准号: 3458924
• 负责人: LLOYD GRAY
• 金额: $ 8.68万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 1988
• 资助国家: 美国
• 起止时间: 1988-05-05 至 1993-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3458924
• 关键词: G protein; T lymphocyte; acidity /alkalinity; antibody dependent killer cell; biological signal transduction; calcium transporting ATPase; cinemicrography; cyclic AMP; cytolysis; flow cytometry; fluorescence spectrometry; inositol phosphates; ion transport; laboratory mouse; laboratory rat; membrane channels; membrane potentials; neoplasm /cancer immunology; phosphoproteins

The long term goal of this proposal is to arrive at a comprehensive understanding of the mechanism of signal transduction and lethal hit delivery in cytolytic T lymphocytes (CTL). CTL are an ultimate effector cell in the cellular arm of the immune response and are involved in host defense from neoplasia and viral illness as well as graft rejection and graft-vs-host disease. Thus, the mechanism by which these cells are activated to produce these effects is of fundamental biomedical importance. The Specific Aims of this proposal are: 1. to relate the functionally important transmembrane fluxes of Ca2+, K+ and C1- to one another and to changes in membrane potential and intracellular pH to determine mechanisms of control of these events and the consequences of their occurrence, and; 2. to examine the role of cAMP and inositol polyphosphates (IP) in lytic function and to relate changes in the intracellular concentrations of these second messengers to ion fluxes as well as to determine the possible role of cAMP in control of protein phosphorylation and antigen induced morphologic changes in CTL. These studies will use fluorescence spectroscopy, flow cytofluorimetry, and high resolution cinemicrography to document the involvement of ionic species in CTL mediated lysis and to relate these events to morphological changes which accompany the lytic process. Additionally, various pharmacological agents will be used to inhibit cytolysis by distinct mechanisms. Phosphoprotein analysis, measurement of intracellular cAMP and IP as well as analysis of G protein involvement will be conducted to relate various inhibitory manipulations to known regulatory pathways. These observations will be synthesized into a pathway leading from target cell binding to cytolysis.

该提议的长期目标是实现全面 了解信号转导和致命命中的机制 在细胞溶解T淋巴细胞（CTL）中递送。 CTL是最终效应器 免疫反应的细胞臂中的细胞，并参与宿主 防御肿瘤和病毒疾病以及移植的拒绝和 移植-VS宿主疾病。 因此，这些细胞是 激活以产生这些影响是基本的生物医学重要性。 该提案的具体目的是：1。 Ca2+，K+和C1-的重要跨膜通量彼此，然后 膜电位和细胞内pH的变化以确定机制 控制这些事件及其发生的后果，以及； 2。 检查cAMP和肌醇多磷酸盐（IP）在裂解中的作用 功能并关联这些细胞内浓度的变化 第二使者到离子通量，并确定可能的作用 控制蛋白质磷酸化和抗原诱导形态学的cAMP CTL的变化。 这些研究将使用荧光光谱，流量 细胞荧光法和高分辨率摄影记录 离子物种参与CTL介导的裂解，并将其联系起来 伴随裂解过程的形态变化的事件。 此外，将使用各种药理剂来抑制 通过不同机制的细胞解析。 磷蛋白分析，测量 细胞内营地和IP以及G蛋白受累的分析将 进行以将各种抑制作用与已知调节性联系起来 途径。 这些观察结果将被合成为前进的途径 从靶细胞结合到胞解。