Lipid Signaling in Chemotaxis

趋化作用中的脂质信号传导

• 批准号: 8325132
• 负责人: Miho Iijima
• 金额: $ 30.54万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-30 至 2014-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8325132
• 关键词: 1-Phosphatidylinositol 3-Kinase; Actins; Arthritis; Asthma; Atherosclerosis; Binding; Binding Proteins; Biochemistry; Biological Assay; Biological Models; Cell membrane; Cells; Cellular biology; Chemicals; Chemotactic Factors; Chemotaxis; Complex; Cytoskeleton; Defect; Development; Dictyostelium; Dictyostelium discoideum; Disease; Eukaryotic Cell; Event; Experimental Models; Genes; Genetic; Goals; Guanine Nucleotide Exchange Factors; Human body; In Vitro; Inflammation; Lead; Life; Link; Lipids; Maintenance; Malignant Neoplasms; Mediating; Molecular; Morphogenesis; Neoplasm Metastasis; Outcome; PH Domain; PTEN gene; Pathogenesis; Pathway interactions; Phosphatidylinositols; Phospholipase A2; Phosphoric Monoester Hydrolases; Phosphorylation; Physiological; Play; Postdoctoral Fellow; Process; Production; Protein Binding; Proteins; Proteomics; Regulation; Research; Research Proposals; Role; Signal Pathway; Signal Transduction; Signaling Molecule; Source; Surface; Tissues; Translating; Two-Hybrid System Techniques; Work; Wound Healing; Yeasts; axon guidance; base; cancer therapy; cell motility; cellular imaging; extracellular; genetic regulatory protein; genome wide association study; genome-wide; human Huntingtin protein; human disease; in vivo; insight; member; novel; phosphoinositide-3,4,5-triphosphate; polymerization; professor; public health relevance; ran-binding protein 1; response; rho GTP-Binding Proteins; tripolyphosphate; tumor

DESCRIPTION (provided by applicant): Chemotaxis, a process in which cells migrate toward higher concentrations of chemoattractants, is important for a variety of physiological events such as axon guidance, wound healing, and tissue morphogenesis. Inappropriate chemotaxis leads to many human diseases including tumor metastasis, asthma, arthritis and atherosclerosis. The long-term goal of our research is to reveal the molecular mechanism of chemotaxis and to understand the pathogenesis of chemotaxis- related human diseases. Using Dictyostelium discoideum as our experimental model system, we have demonstrated that phosphatidylinositol 3,4,5 triphosphate (PIP3) plays a critical role for intracellular signaling in chemotaxis. PIP3 is highly enriched at the leading edge of cells and activates downstream signaling events such as remodeling of the actin cytoskeleton. We have demonstrated that the intracellular level and localization of PIP3 are regulated by a lipid phosphatase, PTEN. PTEN is located at the rear end of chemotaxing cells and restricts the production of PIP3 at the leading edge. The local accumulation of PIP3 stimulates actin polymerization to extend pseudopods toward the source of chemoattractant. To date, it is unknown how the localization and activity of PTEN are regulated, and how PIP3 signaling is translated into reorganization of the actin cytoskeleton. In this research proposal, we will use a combination of genetics, biochemistry, cell biology and proteomics to achieve the following specific aims: 1) To determine how phosphorylation regulates the localization and activity of PTEN; 2) To define the functions of two proteins required for chemotaxis - Huntingtin and GxcT, a novel guanine nucleotide exchange factor for Rho GTPases; 3) To identify novel components that link PIP3 signaling and the actin cytoskeleton using proteomic approaches as well as genome-wide characterization of PH-domain containing proteins. The outcomes of our research are expected to provide novel insights into molecular mechanisms of chemotaxis and may lead to development of chemotaxis-based treatments for cancer and inflammation. PUBLIC HEALTH RELEVANCE: We study chemotaxis, a process in which cells sense extracellular chemical compounds and move toward the source of chemicals. Chemotaxis is highly relevant to development and maintenance of healthy human body as well as the pathogenesis of many diseases such as cancer, asthma, arthritis and atherosclerosis. The long-term goal of our study is to understand how chemotaxis works and how defects in chemotaxis cause human diseases using a variety of approaches including genetics, biochemistry, cell biology and proteomics.

描述(申请人提供)：趋化是细胞向更高浓度的趋化物质迁移的过程，对于轴突引导、伤口愈合和组织形态形成等各种生理事件非常重要。不适当的趋化作用会导致许多人类疾病，包括肿瘤转移、哮喘、关节炎和动脉粥样硬化。我们研究的长期目标是揭示趋化的分子机制，了解与趋化相关的人类疾病的发病机制。以盘基网柄菌为实验模型系统，我们证明了磷脂酰肌醇3，4，5-三磷酸(PIP3)在趋化作用的细胞内信号转导中起着关键作用。PIP3在细胞前沿高度富含，并激活下游信号事件，如肌动蛋白细胞骨架的重塑。我们已经证明了PIP3在细胞内的水平和定位是由一种脂质磷酸酶PTEN调节的。PTEN位于趋化细胞的后端，在前沿限制PIP3的产生。PIP3的局部积聚刺激肌动蛋白聚合，使伪足向趋化物质的来源延伸。到目前为止，还不清楚PTEN的定位和活性是如何调节的，以及PIP3信号是如何翻译成肌动蛋白细胞骨架的重组的。在这项研究中，我们将结合遗传学、生物化学、细胞生物学和蛋白质组学来实现以下具体目标：1)确定磷酸化如何调节PTEN的定位和活性；2)确定趋化所需的两个蛋白质-Huntingtin和GxcT的功能，GxcT是一种新的Rho GTP酶的鸟嘌呤核苷酸交换因子；3)使用蛋白质组学方法鉴定连接PIP3信号和肌动蛋白细胞骨架的新组件，并对含有PH结构域的蛋白质进行全基因组表征。我们的研究结果有望为趋化的分子机制提供新的见解，并可能导致基于趋化的癌症和炎症治疗的发展。 公共卫生相关性：我们研究趋化性，这是一个细胞感觉到细胞外化合物并向化学物质来源移动的过程。趋化性与健康人体的发育和维持以及癌症、哮喘、关节炎和动脉粥样硬化等多种疾病的发病密切相关。我们研究的长期目标是使用包括遗传学、生物化学、细胞生物学和蛋白质组学在内的各种方法来了解趋化作用是如何工作的，以及趋化作用缺陷是如何导致人类疾病的。