Systematic dissection of gut cellular circuits [at single cell resolution]
Systematic dissection of gut cellular circuits [at single cell resolution]
批准号:
9753218
负责人:
Daniel Bartholomew Graham
金额:
$179.6万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-01 至 2022-07-31
关键词:
AddressAffectAntigensAtlasesAutoimmunityBacterial InfectionsBindingBiological ProcessBiopsyCell Differentiation processCell LineageCell physiologyCellsClinicalCollaborationsCommunicable DiseasesCommunicationCommunitiesComplexComputational BiologyComputer AnalysisDataData AnalysesDietDietary FactorsDiseaseDissectionEndocrineEndocrine systemEnteralEnvironmentEpithelialEpithelial CellsEpitheliumEvolutionExcisionFood HypersensitivityGap JunctionsGene Expression ProfileGenetic studyGenomic approachGenomicsGut MucosaHealthHematopoieticHomeostasisHumanHuman ActivitiesImmune responseImmunityImmunologyIndividualInfectionInflammationInflammatoryInflammatory Bowel DiseasesInflammatory disease of the intestineInstitutesIntestinesLiquid substanceMalignant NeoplasmsMapsModelingMolecularMolecular GeneticsMucosal ImmunityMucous MembraneMusNeuronsNutrientOrganPathologicPathologyPathway interactionsPatientsPhysiologicalPositioning AttributeResearch PersonnelResolutionSalmonella infectionsSamplingSeriesSiteSmall IntestinesSpecimenStem cellsSystemT-LymphocyteTestingTissuesValidationWorkbody systemcell typegastrointestinal epitheliumgenetic manipulationhelminth infectionhuman diseasehuman pathogeninnovationinsightintercellular communicationmulti-scale modelingnovelpathogenresponsetranscriptomeuptake
中文摘要
点击翻译按钮获取中文摘要
英文摘要
ABSTRACT
The gut serves as a nexus that connects and integrates organ systems throughout the body, with far-reaching
consequences in health and disease. The biological function of the gut as an organ is the result of complex
interactions between dynamic and heterogeneous cell types. Any pathological insult to the gut, such as barrier
breach or infection, must be met with a response that is appropriate and proportional to the insult, such that
homeostasis is re-established. In this application, we propose novel single-cell genomic approaches to
decipher heterogeneous cellular responses to inflammatory challenge. Through a series of functional genetics
studies, we aim to elucidate the molecular basis of mucosal immunity in the context of pathological
inflammation. Towards this end, we propose the following specific aims:
Aim 1. Comprehensively define all cell lineages and dynamic functional states in intestinal inflammation.
Aim 2. Delineate intercellular communication networks that coordinate intestinal inflammation.
Aim 3. Identify disease modifier pathways in human biopsies and integrate with intercellular communication
networks.
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会议论文
Identification and Characterization of Microbial Metabolites in Immunity
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批准号:10629379
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项目类别:
-
资助金额:$79.38万
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财政年份:2022
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负责人:Daniel Bartholomew Graham
-
依托单位:
Identification and Characterization of Microbial Metabolites in Immunity
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批准号:10513037
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项目类别:
-
资助金额:$78.31万
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财政年份:2022
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负责人:Daniel Bartholomew Graham
-
依托单位:
Systematic dissection of gut cellular circuits [at single cell resolution]
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批准号:9380153
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项目类别:
-
资助金额:$179.6万
-
财政年份:2017
-
负责人:Daniel Bartholomew Graham
-
依托单位:
海外基金