CONTROLLING NK CELL ANTI-CANCER ACTIVITY: THE ROLE OF NUTRIENTS AND SUPPLEMENTS
CONTROLLING NK CELL ANTI-CANCER ACTIVITY: THE ROLE OF NUTRIENTS AND SUPPLEMENTS
批准号:
8445901
负责人:
MARCO COLONNA
金额:
$16.53万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2014-12-31
关键词:
AddressApplications GrantsAryl Hydrocarbon ReceptorAzoxymethaneBindingBotanicalsCell LineCellsChemicalsChronicColitisColonCountryDataDendritic CellsDevelopmentDietDysplasiaEpithelialEpithelial Cell ProliferationEpithelial CellsFlavonoidsGene MutationHumanImmuneImmunityImmunologic MonitoringIndolesInflammatoryInterferonsInterleukin-12Interleukin-2LaboratoriesLamina PropriaLesionLeukocytesMalignant NeoplasmsMeasuresMediatingMelanoma CellMesenteryMethanolModelingMouse StrainsMucous MembraneMusNatural Killer CellsNutrientNutritionalOligonucleotidesPhenotypePlasticsPlayPositioning AttributeProductionPropertyQuercetinReagentRecording of previous eventsRoleSmall IntestinesSodium Dextran SulfateStimulusStructure of aggregated lymphoid follicle of small intestineSupplementationTestingTherapeuticTransplantationWorkaryl hydrocarbon receptor ligandbasecancer preventioncancer therapycell typechemokinecytokinedietary supplementsfeedingfruits and vegetablesin vivointerleukin-22lymph nodesmelanomamouse modelnovelpolyphenolpublic health relevanceresearch studysubcutaneoustooltranscription factortumortumor growthtumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Natural killer cells are generally viewed as a first line of defense in cancer immunosurveillance and are critical players in immune-mediated cancer rejection. We have recently described a new subset of unconventional NK cells that reside in mucosal tissues and are characterized by production of large amounts of IL-22. We refer to this novel cell subset as NK-22. Although the origin of these cells is still unclear and their relationship to conventional NK cells a matter of debate, we and others have shown that these cells can acquire features typical of conventional NK cells when exposed to inflammatory cytokines. Moreover, recent work has suggested that a similar cell type plays a critical role in initiating tumor rejection. Our preliminary data show that NK-22 are highly dependent on the transcription factor aryl hydrocarbon receptor (AHR) for their development. AHR is known to bind dietary compounds such as indol-3-carbinol (I3C) and flavonoids that are associated with anti-tumor activity. We hypothesize that by engaging AHR through dietary supplements, we can manipulate the numbers and or the activity of NK-22. In Specific Aim 1 we will test the effect of I3C and the flavonoid quercetin on NK-22 expansion and function in vivo. In Specific Aim 2 we will determine whether these supplements impact the anti-tumor function of NK-22 in spontaneous and transplantable tumor models. We discovered NK-22, contributed to the initial characterization of their development and function and have generated unique NK-22 specific reagents as well as mouse strains lacking NK-22 or AHR in several immune and non-immune cell types. Therefore, we are in a unique position to directly test the impact of specific dietary supplements allegedly associated with anti-cancer activity on tumor surveillance by innate immune cells. !
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