grant

Control of adipose immune-stromal niche topography in obesity

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 1 Sept 2024Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY202521+ years old3-D3-Dimensional3DAbdominal obesityAdipocytesAdipose CellAdipose tissueAdultAdult HumanAdult-Onset Diabetes MellitusAdvisory CommitteesAffectAmericanAndroid fat distributionAnimal FeedAnimalsApoplexyAppearanceArchitectureAsystoleAutoregulationAwardB cell differentiation factorB cell growth factorB cell stimulating factor 2B-Cell Differentiation FactorB-Cell Differentiation Factor-1B-Cell Differentiation Factor-2B-Cell Growth Factor-1B-Cell Growth Factor-IB-Cell Proliferating FactorB-Cell Stimulating FactorB-Cell Stimulating Factor-1B-Cell Stimulation Factor-1B-Cell Stimulatory Factor-1B-Cell Stimulatory Factor-2B220BCDFBCDF-1BCGFBCGF-1BCSF 1BSF-1BSF-2BSF1BSF2BinetrakinBiological Response ModifiersBiometricsBiometryBiomodulatorsBiostatisticsBlood capillariesBody TissuesBrain Vascular AccidentCD124CD45Caloric IntakeCardiac ArrestCardiac infarctionCardiovascularCardiovascular Body SystemCardiovascular DiseasesCardiovascular Organ SystemCardiovascular systemCell BodyCell Communication and SignalingCell Mediated ImmunologyCell SignalingCell TherapyCell-Mediated ImmunityCellsCellular ImmunityCentral obesityCentripetal obesityCerebral StrokeCerebrovascular ApoplexyCerebrovascular StrokeCharacteristicsChronicClinical PathologyCollaborationsCollagenConfocal MicroscopyCrownsDataData ScienceDepositDepositionDevelopmentDevelopment PlansDiabetes MellitusDiseaseDisorderDistressDoctor of PhilosophyEctopic lymphoid organEctopic lymphoid structureEnergy IntakeEngineering / ArchitectureEnvironmentEpidemicEventExpenditureFat CellsFatsFatty TissueFatty acid glycerol estersFellowshipFibroblastsFibrosisFlow CytofluorometriesFlow CytofluorometryFlow CytometryFlow MicrofluorimetryFlow MicrofluorometryFoundationsFundingFutureGP180GoalsHPGFHealthHeart ArrestHeart VascularHematopoieticHepatocyte-Stimulating FactorHigh Fat DietHomeostasisHumanHybridoma Growth FactorHyperglycemiaIFN-beta 2IFNB2IL-1IL-13IL-4IL-6IL1IL13IL1RIL1R1IL1R1 geneIL1RAIL4 ProteinIL4RIL4R geneIL4RAIL6 ProteinImmuneImmune MediatorsImmune Mediators/ModulatorsImmunesImmunityImmunologyImmunomodulationInfiltrationInflammationInflammatoryInsulin ResistanceInterleukin IInterleukin-1Interleukin-13Interleukin-4Interleukin-4 PrecursorInterleukin-6Intracellular Communication and SignalingInvestigationKetosis-Resistant Diabetes MellitusKnock-outKnockoutKnowledgeLY5LeannessLinkLipocytesLoxP-flanked alleleLymphatic cellLymphocyteLymphocyte Stimulatory Factor 1Lymphocyte-Stimulating HormoneLymphocyticLymphoidLymphoid CellMCGF-2MGI-2MacrophageMacrophage Cell FactorMast Cell Growth Factor-2Mature LipocyteMature fat cellMaturity-Onset Diabetes MellitusMeasuresMentorshipMetabolicMetabolic dysfunctionMiceMice MammalsModern ManMolecularMurineMusMyeloid Differentiation-Inducing ProteinMyocardial InfarctMyocardial InfarctionMyofibroblastNIDDMNational Institutes of HealthNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusObese MiceObesityOutcomeOvernutritionPTPRCPTPRC genePathologicPeritonealPh.D.PhDPhysiciansPhysiological HomeostasisPlasmacytoma Growth FactorPopulationProfibrotic factorProfibrotic signalProliferatingReceptor ProteinRegulatory T-LymphocyteResearchResearch EthicsResidenciesRisk FactorsSamplingScientistSignal TransductionSignal Transduction SystemsSignalingSlow-Onset Diabetes MellitusStable Diabetes MellitusStrokeStructureSurfaceSurvey InstrumentSurveysT Helper FactorT cell infiltrationT-Cell Growth Factor 2T2 DMT200T2DT2DMTask ForcesTertiary lymphoid structureTestingThickThicknessThinnessTimeTissue ExpansionTissuesTraining ProgramsTregTruncal obesityType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesUnited States National Institutes of HealthVisceralWeightWorkadiposeadiposityadult onset diabetesadulthoodadvisory teamangiogenesisanimal foodantibody conjugatebiological signal transductionbrain attackcaloric dietary contentcapillarycardiac infarctcardiovascular disordercareer developmentcell based interventioncell mediated interventioncell mediated therapiescell-based therapeuticcell-based therapycellular therapeuticcellular therapycerebral vascular accidentcerebrovascular accidentcirculatory systemcoronary attackcoronary infarctcoronary infarctioncorpulencecytokinedevelopmentaldiabetesflow cytophotometryfloxedfloxed alleleglucose toleranceheart attackheart infarctheart infarctionhelminth infectionhelminthic infectionhemopoietichyperglycemicimmune modulationimmune regulationimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryin vivoinfected with helminthinsulin resistantinsulin toleranceinterferon beta 2ketosis resistant diabeteslymph celllymphocyte activating factormaturity onset diabetesmulti-modalitymultidisciplinarymultimodalitynovelob/ob mouseobese individualsobese peopleobese personobese populationobese subjectsobesity developmentobesity interventionobesity managementobesity preventionobesity therapyobesity treatmentprevent obesityprogramspromoterpromotorreceptorregulatory T-cellsresponsespatial and temporalspatial temporalspatiotemporalstrokedstrokestertiary lymphoid organtherapeutic agent developmenttherapeutic developmenttherapeutic targetthree dimensionaltissue maptissue mappingtransfusion medicinetype 2 DMtype II DMtype two diabetesvisceral obesityweightswhite adipose tissueyellow adipose tissue
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Full Description

PROJECT SUMMARY
Obesity affects nearly half of the adult US population and is a risk factor for adverse cardiovascular events

such as stroke and cardiac arrest, and Type II diabetes. Obesity promotes inflammation of the visceral adipose

tissue (VAT), which in turn drives hyperglycemia, insulin resistance, and contributes to cardiovascular

inflammation. Therefore, my long-term research goal is understanding the breakdown of tissue homeostatic

mechanisms in the VAT, which may help understand and lead to treatments that constrain the development of

obesity-associated inflammation.

The overall objective of this proposal is to delineate adipose tissue topography using a multimodal

approach through spatial sequencing, thick section confocal microscopy and flow cytometry to identify novel

signaling or cell populations as therapeutic targets for treatment of obesity-associated inflammation. Profiling

stromal and immune cells in the eVAT, I’ve shown their close association and remodeling during high fat diet.

Based on these data, my central hypothesis is that obesity alters eVAT tissue topography, thus bringing

together signaling partners that drive inflammatory and pro-fibrotic reprogramming responsible for resident

lymphoid and body-wide metabolic dysfunction. I propose to study the spatial and temporal relationships among

immune and fibroblasts in obesifying eVAT in two aims. In Aim 1, I will topographically delineate fibroblast

contributions to obese tissue architecture and in Aim 2, I will assess immune cell contribution and identify unique

cellular signatures and interactions in mouse and human adipose using spatial sequencing.

Having completed my MD PhD and residency in Clinical Pathology and fellowship in Cellular Therapy

and Transfusion Medicine, I am now pursuing research as an R38-funded StARR scholar. I am applying for the

K38 StARRTS Award to support my goal of becoming an independent physician-scientist. The exceptional

training program at UCSF, especially in the immunology and obesity fields, will support my effort. Key parts of

my training program leverage several aspects of this environment, including mentorship by Dr Ari Molofsky, an

expert in tissue immune and stromal niches; co-mentorship by Dr Richard Locksley, an expert in Type 2

immunity, and in vivo immunology; co-mentorship by Dr Suneil Koliwad, an expert in obesity-associated

inflammation and diabetes; guidance by a multidisciplinary advisory committee and collaborations with Drs Mike

Rosenblum and Dean Sheppard, experts in spatial sequencing and fibrosis, respectively; coursework in data

science, biostatistics, and research ethics; and professional development activities. Altogether, this career

development plan will establish a strong foundation for me to unravel mechanisms of obesity-associated

inflammation and for advancing towards an independent research program as a physician-scientist.

Grant Number: 5K38HL175025-02
NIH Institute/Center: NIH

Principal Investigator: Joanna Balcerek

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