Core D: Cell Function Analysis Core
核心D:细胞功能分析核心
基本信息
- 批准号:8441164
- 负责人:
- 金额:$ 17.42万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:AdipocytesBiological AssayBiosensorCell SurvivalCell physiologyCellsConsultationsConsumptionCyclic AMP-Dependent Protein KinasesD CellsDetectionDiabetes MellitusDiseaseEndothelial CellsEquipmentEvaluationFunctional disorderFundingGlucoseGoalsHepatocyteHumanImageIslet CellLymphocyteManuscriptsMeasurementMembrane PotentialsMetabolicMetabolismMitochondriaMonkeysMuscle satellite cellNeuronsObesityPathogenesisPathway interactionsPeer Review GrantsPhysiologyProductionProtein Kinase CPublicationsRadiolabeledRegulationResearchResearch PersonnelRetinaRodentRoleServicesSignal TransductionSkeletal MuscleSystemTimeTissuesTrainingUniversitiesWashingtonanalytical toolbasecell typecytochrome cglucose metabolismisletmacrophagemeetingsmetabolic abnormality assessmentmetabolomicsminimally invasivemitochondrial membranepeptide hormoneradiotracer
项目摘要
The overall objective of the Cell Function Analysis Core at the University of Washington Diabetes
Research Center is to provide affiliates with analyses of glucose metabolism, mitochondrial function and
intracellular signaling components critically important in diabetes, obesity and related disorders. To achieve
this goal, the Core aims to: (1) Provide real time functional analysis in flow culture systems of tissues and
cell types important in diabetes research. These have been expanded from just islets, to include retina,
skeletal muscle, stem cells, macrophages, lymphocytes, adipocytes, endothelial cells, neuronal cells and
hepatocytes; (2) Provide static assessment of cellular metabolism and function; (3) Isolate and culture
primary tissue from rodents including islets and islet cells for subsequent morphological and functional
characterization. Further, to procure human and monkey islets for the same purposes; and (4) Offer training
and consultation to affiliates, their trainees and staff as well as develop new analytical tools requested by
affiliates to support their studies of the metabolic regulation of cell function. The expansion of services
provided during the current funding cycle has allowed the Core to better serve the needs of the Center's
research base. As diabetes perturbs cellular metabolism and signaling in a variety of;cell types, the services
of the Cell Function Analysis Core are, and will continue to be, of great value to Diabetes Research Center
affiliate investigators who wish to study these aspects in order to gain a better understanding of physiology
and disease pathophysiology.
RELEVANCE
华盛顿糖尿病大学细胞功能分析中心的总体目标
研究中心为附属机构提供葡萄糖代谢、线粒体功能和
在糖尿病、肥胖症和相关疾病中至关重要的细胞内信号传导组分。实现
该核心旨在:(1)在组织的流动培养系统中提供真实的时间功能分析,
细胞类型在糖尿病研究中很重要。这些已经从仅仅是胰岛扩展到包括视网膜,
骨骼肌、干细胞、巨噬细胞、淋巴细胞、脂肪细胞、内皮细胞、神经元细胞和
肝细胞;(2)提供细胞代谢和功能的静态评估;(3)分离和培养
来自啮齿动物的初级组织,包括胰岛和胰岛细胞,用于随后的形态和功能研究。
特征化此外,采购人类和猴子的胰岛用于相同的目的;以及(4)提供培训
为附属机构、其受训人员和工作人员提供咨询,
支持他们对细胞功能代谢调节的研究。服务的扩展
在目前的供资周期内提供的资金使核心能够更好地满足中心的需求,
研究基地。由于糖尿病扰乱了多种细胞类型的细胞代谢和信号传导,
细胞功能分析核心是,并将继续是,糖尿病研究中心的巨大价值
希望研究这些方面以更好地了解生理学的附属研究者
和疾病病理生理学。
相关性
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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{{ truncateString('IAN R SWEET', 18)}}的其他基金
Mechanism and Assessment of Hypoxia-Induced Islet Death
缺氧引起的胰岛死亡的机制和评估
- 批准号:
6863682 - 财政年份:2004
- 资助金额:
$ 17.42万 - 项目类别:
Mechanism and Assessment of Hypoxia-Induced Islet Death
缺氧引起的胰岛死亡的机制和评估
- 批准号:
6707020 - 财政年份:2004
- 资助金额:
$ 17.42万 - 项目类别:
INTEGRATIVE APPROACH TO UNDERSTAND ETIOLOGY & CAUSES OF TYPE II DIABETES
了解病因的综合方法
- 批准号:
6119782 - 财政年份:1998
- 资助金额:
$ 17.42万 - 项目类别:
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