UC Irvine AD Translational Center for Disease Model Resources-Microbiome Supplement
UC Irvine AD Translational Center for Disease Model Resources-Microbiome Supplement
批准号:
9932650
负责人:
FRANK M LAFERLA
金额:
$39.04万
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:
2017-09-15 至 2022-08-31
关键词:
3xTg-AD mouseAgeAlzheimer disease preventionAlzheimer&aposs DiseaseAlzheimer&aposs disease modelAnimal Disease ModelsAnimal DiseasesAnimal ModelAnimalsAppearanceAreaBehaviorBiochemicalCecumDataData CollectionDementiaDevelopmentDiseaseDisease ProgressionDisease modelElderlyEnsureExposure toFutureGenderGene ExpressionGenerationsGoalsHumanInflammationInvestigationMeasuresMicrobeModelingMultivariate AnalysisMusNeurodegenerative DisordersNeurofibrillary TanglesOnset of illnessPathologyPhysiologyPlayProcessReproducibilityResourcesRoleSamplingSenile PlaquesSiteStudy modelsTimeTransgenic Organismsaging brainanimal facilitybasecohortdesignearly onsetfecal metabolomefecal microbiomegerm free conditionmetabolomemicrobialmicrobial communitymicrobiomemicrobiome analysismouse modelneuroinflammationneuron losssex
中文摘要
项目总结/文摘
英文摘要
Project Summary/Abstract
Alzheimer’s disease (AD) is characterized by the progressive appearance of amyloid plaques and
neurofibrillary tangles, leading to neuroinflammation, neuronal loss and dementia. Microbial
exposures modulate inflammation, and are now known to impact the onset and progression AD in
both animal models and humans. However, the microbiomes of the UCI MODEL-AD animals are not
currently being studied. Characterizing longitudinal microbiomes of MODEL-AD animals will have
important impact in understanding disease progression as well ensuring the rigor and reproducibility
of AD studies in animal cohorts that may have different microbiomes in different animal facilities or
even different cages. Microbes and their metabolites may be part of AD prevention and treatment in
the future. We therefore propose to pilot the generation of microbiome and metabolome data from
fecal and cecal samples in young as well as older mice to characterize (a) longitudinal microbial
community composition, (b) longitudinal metabolite composition, and (c) disease-associated microbes
and metabolites. We will include cohorts of the early onset 5xFAD, late onset hAb-KI, the triple
transgenic (3xTg-AD) mice that develop both plaque and tangle pathology, and several collaborative
crosses along with WT controls. This will allow us to determine if there are microbes associated with
each model, which timepoints and sample types are most associated with AD relevant physiology,
and whether microbiome and metabolome markers will be useful in future studies. Microbiome data
from UCI will be compared with microbiome data being generated at the other MODEL-AD sites.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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依托单位:
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依托单位:
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依托单位:
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