Generation of a Cellular Atlas of Adipose Tissue in Mouse and Man
Generation of a Cellular Atlas of Adipose Tissue in Mouse and Man
批准号:
9906217
负责人:
DIANE J MATHIS
金额:
$172.49万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-04-23 至 2023-03-31
关键词:
AddressAdipocytesAdipose tissueAffectAgeAnatomyAnteriorAtlasesBehaviorBiological AssayBiologyBiopsyBody Weight decreasedCell CommunicationCell SeparationCell physiologyCellsCellular StructuresCoculture TechniquesCommunitiesComplexComputational TechniqueCytokine ReceptorsDataDatabasesDevelopmentDiseaseEndothelial CellsFastingFatty acid glycerol estersFibroblastsFractionationFutureGastric BypassGenerationsGenesGoalsGrowthHealthHeterogeneityHigh Fat DietHumanImmuneIndividualIndividual DifferencesKnowledgeLocationMesenteryMetabolicMetabolismModelingMusNutritionalObesityOrganismPathway AnalysisPathway interactionsPlayPopulationResolutionResourcesRoleStressStructureSurfaceT-Cell ActivationTechniquesTechnologyThinnessTissuesVisceralWeight Gainbariatric surgerybasecell typecost effectivedifferential expressionexperimental studyfeedinggenome wide association studyhuman subjectin vivolipid biosynthesismacrophagemanmenmetabolic abnormality assessmentnetwork modelsnext generationnovelresponsesexsingle cell sequencingsingle-cell RNA sequencingsubcutaneousthermal stresstranscriptome
中文摘要
摘要
脂肪组织在调节全身代谢中起关键作用。脂肪储存库本身
是细胞类型的异质混合物,包括免疫细胞、前脂肪细胞、基质细胞、
成纤维细胞、内皮细胞和其他细胞,以及脂肪细胞本身。的相对
已知这些细胞的比例以及它们的激活状态在以下变化中不同:
营养状态尽管长期以来人们认识到脂肪组织的行为是由
通过脂肪垫内各种组成细胞类型之间的相互作用,
不幸的是,这些细胞亚群的身份是不完全的。在这里,我们建议使用单细胞
用于鉴定小鼠不同脂肪库内的新细胞亚群的测序技术
还有人类我们将评估这些不同的细胞如何随性别、年龄和代谢紊乱而变化,
如禁食、高脂肪饮食、胃旁路术和热应激。此外,我们将确定激活
这些细胞在这些不同条件下的状态,并将利用各种实验和
计算技术来表征细胞类型之间发生的相互作用。所得
数据库将是一个社区资源和脂肪组织生物学新时代的起点。
英文摘要
ABSTRACT
Adipose tissue plays a critical role in regulating systemic metabolism. The adipose depots themselves
are heterogeneous mixtures of cell types that include immune cells, preadipocytes, stromal
fibroblasts, endothelial cells, and others, in addition to the adipocytes themselves. The relative
proportions of these cells, as well as their activation state, is known to differ following changes in
nutritional state. Despite a longstanding realization that the behavior of adipose tissue is determined
by interactions between the various component cell types within the fat pad, our knowledge of the
identity of these cellular sub-populations is woefully incomplete. Here we propose to use single cell
sequencing technology to identify novel subpopulations of cells within different adipose depots of mice
and humans. We will assess how these different cells vary with sex, age, and metabolic perturbations,
like fasting, high fat diet, gastric bypass, and thermal stress. Further, we will determine the activation
state of these cells under these different conditions, and will utilize a variety of experimental and
computational techniques to characterize the interactions that occur between cell types. The resulting
database will be a community resource and the starting point for a new era of adipose tissue biology.
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