grant

Islet and Pancreas Analysis Core

Organization VANDERBILT UNIVERSITY MEDICAL CENTERLocation NASHVILLE, UNITED STATESPosted 1 Dec 1996Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY2025AbbreviationsAcademic Medical CentersAchyroclineAgingAnimalsArchitectureAreaAssayAutoregulationB9 endocrine pancreasBasal Transcription FactorBasal transcription factor genesBioassayBiological AssayBiologyBody TissuesBrittle Diabetes MellitusCell BodyCell Communication and SignalingCell DifferentiationCell Differentiation processCell SignalingCellsCellular MorphologyChromosomal, Gene, or Protein AbnormalityComplementComplement ProteinsComplexConstitutionCytogenetic or Molecular Genetic AbnormalityDetectionDevelopmentDiabetes MellitusDiseaseDisorderDysfunctionEndocrine PancreasEngineering / ArchitectureFunctional disorderFundingGeneral Transcription Factor GeneGeneral Transcription FactorsGeneticGenetic AbnormalityHistologicHistologicallyHomeostasisHormone secretionHumanIDDMImageImage AnalysesImage AnalysisImage EnhancementImmunologyIn VitroIndividualInfrastructureInsulin-Dependent Diabetes MellitusIntermediary MetabolismIntracellular Communication and SignalingInvestigatorsIslands of LangerhansIslands of Langerhans TransplantationIslands of Pancreas TransplantationIslets of LangerhansIslets of Langerhans GraftingIslets of Langerhans TransplantationJuvenile-Onset Diabetes MellitusKetosis-Prone Diabetes MellitusLocationMaintenanceMarcelaMeasurementMetabolicMetabolic ProcessesMetabolismMiceMice MammalsModern ManMolecularMolecular AbnormalityMurineMusNIDDKNational Institute of Diabetes and Digestive and Kidney DiseasesNesidioblastsPancreasPancreaticPancreatic IsletsPancreatic Islets TransplantationPars endocrina pancreatisPhenotypePhysiologicPhysiologicalPhysiological HomeostasisPhysiologyPhysiopathologyProceduresProcessPublishingRadioimmunoassayRadioimmunoassay ImmunologicResearchResearch PersonnelResearch ResourcesResearchersResolutionResourcesRodentRodentiaRodents MammalsServicesSignal TransductionSignal Transduction SystemsSignalingStandardizationSudden-Onset Diabetes MellitusT1 DMT1 diabetesT1DT1DMTechniquesTechnologyTissuesTrainingTranscription Factor Proto-OncogeneTranscription factor genesType 1 Diabetes MellitusType 1 diabetesType I Diabetes MellitusUniversity Medical CentersWorkanalytical toolautologous islet transplantationbeta cell developmentbio-imagingbioimagingbiological signal transductionblood glucose regulationcell morphologycell typecellular differentiationcomplementationcostdevelopmentaldiabetesendocrine pancreas developmentflexibilityflexibleglucose controlglucose homeostasisglucose regulationhormonal secretionhuman tissueimage evaluationimage interpretationimage-based methodimagingimaging methodimaging modalityin vivoindexinginsulin dependent diabetesinsulin dependent type 1isletislet auto transplantationislet beta cell transplantationislet cell transplantislet cell transplantationislet developmentislet transplantationjuvenile diabetesjuvenile diabetes mellitusketosis prone diabetesmolecular aberrationsmultiplexed imagingpancreas developmentpathophysiologyphysiologic stressesphysiologic stressorphysiological stressesprogramsprotein expressionresolutionsresponsesuccesstranscription factortype 1 and type 2 diabetestype I and type II diabetestype I diabetestype one diabeteswhole slide imaging
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Full Description

Islet and Pancreas Analysis Core: Project Summary/Abstract
The Islet and Pancreas Analysis (IPA) Core was established in 2007 as a result of growing demand for murine

islets from Vanderbilt Diabetes Research Center (VDRC) investigators. Over the last funding cycle, the IPA

Core provided services to 47 different investigators (40 Vanderbilt and 7 external nonprofit) by assisting with

4,120 procedures. Research programs within the VDRC encompass the fields of pancreatic islet biology,

development, and function in normal homeostasis and disease, including a broad spectrum of islet-related

processes raging from intracellular signaling, physiological response and adaptation, the immunology of type 1

diabetes, the function of islet-enriched transcription factors, and the maintenance of normal hormone-secreting

status and cell fate. Essential to rigorous research in these areas is the ability to robustly isolate murine islets

and to assay the complex physiological function of both murine and human islets. Vanderbilt has been a

national leader in developing islet functional assays, as evidenced by the selection of the NIDDK-supported

Integrated Islet Distribution Program (IIDP) to house the Human Islet Phenotyping Program (HIPP) at

Vanderbilt under direction of Marcela Brissova, IPA Core Director. The HIPP's location at Vanderbilt has

greatly benefitted VDRC Investigators, allowing newly developed procedures to be seamlessly implemented

through the IPA Core. In addition to offering functional assays, the IPA Core also provides VDRC investigators

with high-resolution, whole-slide image scanners that enable simultaneous analysis of both tissue architecture

and single cell morphology. Numerous VDRC investigators utilize the imaging infrastructure and associated

analytical tools, and in this competitive renewal, the IPA Core proposes the addition of multiplex imaging to

perform high impact, tissue-based studies. While access to this technology is cost-prohibitive and technically

challenging for individual labs, offering it as a core service will significantly enhance the impact of histological

analysis of mouse and human tissue. The IPA Core is also working closely with the Animal Metabolic

Physiology Core (AMPC) to standardize islet transplantation techniques, a valuable experimental resource that

will complement existing ex vivo assays and allow more investigators to perform in vivo studies. Through its

centralized resources and expertise, the IPA Core provides VDRC investigators with reliable and standardized

procedures that facilitate discoveries related to islet biology, cell signaling, and metabolism. The continued

excellence of the IPA Core is crucial to sustain rigorous and impactful work in the areas of pancreas and islet

development and physiology by VDRC investigators.

Grant Number: 5P30DK020593-48
NIH Institute/Center: NIH

Principal Investigator: Marcela Brissova

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