Phospholipase D signaling
Phospholipase D signaling
批准号:
8708111
负责人:
Jie Chen
金额:
$37.43万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-08-01 至 2016-07-31
关键词:
1-Phosphatidylinositol 3-KinaseAmino AcidsBinding SitesBiochemicalCancer Cell Growth RegulationCell Culture SystemCell ProliferationCell physiologyCellular biologyClinicalCollectionComplexCuesD CellsDataFutureGoalsGrowthGrowth FactorGuanosine Triphosphate PhosphohydrolasesHandKnowledgeLaboratoriesLinkLipidsMalignant NeoplasmsMammalian CellMammalsMediatingMediator of activation proteinModelingMolecularMonomeric GTP-Binding ProteinsNutrientPathway interactionsPhosphatidic AcidPhospholipase DPhosphotransferasesPoint MutationPositioning AttributeProteinsPublishingRaptorsReagentRegulationReportingRoleSecond Messenger SystemsSignal PathwaySignal TransductionSirolimusTestingTherapeuticTimeVesicleWorkbasecell growthcell growth regulationcell motilitycombatdrug developmentexperiencehuman diseaseinhibitor/antagonistinterestmTOR proteinmutantnovelresponsesecond messengertooltraffickingtumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Phospholipase D (PLD) and its enzymatic product, the lipid second messenger phosphatidic acid (PA), are critically involved in the regulation of a wide range of mammalian cellular processes, including vesicle trafficking, cell migration, and cell growth/proliferation. Work from our laboratory in recent years has uncovered a connection between PLD/PA and the mammalian target of rapamycin (mTOR) signaling network - a master regulator of cell growth by integrating growth factor and nutrient signals, and an attractive target for drug development against several human diseases including cancer. This pathway from PLD to mTOR has provided a mechanism for the involvement of PLD in cell growth regulation and cancer, and at the same time has implicated the existence of a regulatory network involving PLD1 that is yet to be delineated. In the proposed studies we aim to dissect the molecular wiring of PLD1 signaling, with an emphasis on the role of PLD/PA in the regulation of the rapamycin-sensitive mTOR complex (mTORC1) in response to mitogenic and amino acid signals. Guided by working hypotheses based on our most recent findings, we propose to investigate the mechanisms underlying (1) mitogenic regulation of PLD, (2) amino acid regulation of PLD, and (3) PA regulation of mTORC1. Our experience with both PLD and mTOR signaling studies, our compelling preliminary data, and the unique tools available to us situate us in an ideal position to tackle those important issues. Knowledge gained in these studies will likely have significant impact on our understanding of a signaling network of mechanistic and clinical importance.
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批准号:10729695
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Effect of Local Health Departments on Health Care Disparities for Individuals with Mental Health Disorders
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依托单位:
Single-Molecule Dissection of mTOR Complexes
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批准号:8469719
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资助金额:$14.0万
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财政年份:2013
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依托单位:
Single-Molecule Dissection of mTOR Complexes
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批准号:8738558
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资助金额:$22.09万
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财政年份:2013
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依托单位:
Phospholipase D signaling
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依托单位:
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海外基金