grant

Single-cell epigenomics and transcriptomics of diabetic gastroparesis in humans

Organization MAYO CLINIC ROCHESTERLocation ROCHESTER, UNITED STATESPosted 30 Sept 2021Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2025AddressAffectAutonomic nervous systemB220BehaviorBiopsyBlood leukocyteBody TissuesCD45Cell BodyCellsChromatinChronicCollaborationsComplementComplement ProteinsComplications of Diabetes MellitusDataDiabetes ComplicationsDiabetes MellitusDiabetes-Related ComplicationsDiabetic ComplicationsDiseaseDisorderDistressDuodenumDysfunctionEndocrineEnteralEntericEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessFunctional disorderFutureGP180GastrectomyGastric EmptyingGastric StasisGastroparesisGene ExpressionGenesGrowth AgentsGrowth FactorGrowth SubstancesHarvestHistologicHistologicallyHumanHyperglycemiaIGF1IGF1 geneIGFIImmuneImmunesImmunityImmunologic SubtypingImmunophenotypingImpairmentInflammatoryInnate ImmunityInterstitial Cell of CajalInvoluntary MuscleLY5LeukocytesLeukocytes Reticuloendothelial SystemLinkMarrow leukocyteMetabolicMiceMice MammalsMissionMitochondriaModern ManMolecularMurineMusMuscleMuscle TissueNative ImmunityNatural ImmunityNerve CellsNerve UnitNeural CellNeurocyteNeuronsNon-Specific ImmunityNonspecific ImmunityNuclearOrganOxidative StressPBMCPTPRCPTPRC genePathogenesisPathway interactionsPatientsPeripheralPeripheral Blood Mononuclear CellPhenotypePhysiopathologyProteins Growth FactorsProteomicsRNA SeqRNA sequencingRNAseqRoleSignal PathwaySmooth MuscleStomachSymptomsT200ThickThicknessTissuesUpper GIUpper GI TractUpper Gastrointestinal TractUpper digestive tract structureWhite Blood CellsWhite Cellbench bed sidebench bedsidebench to bed sidebench to bedsidebench to clinicbench to clinical practicecell typecomplementationdelayed gastric emptyingdepositorydesigndesigningdiabetesdiabeticdiabetic gastroparesisepigeneticallyepigenomeepigenomicsexperimentexperimental researchexperimental studyexperimentsgastricgastrointestinal symptomgenome scalegenome-widegenomewideglobal gene expressionglobal transcription profileglycemic controlhistone modificationhyperglycemicimprovedin vivoineffective therapiesineffective treatmentinflammatory environmentinflammatory milieuinsulin signalingmitochondrialmitochondrial dysfunctionmuscularneuronalnew markernitrosative stressnon-ulcer dyspepsianonulcer dyspepsianovel biomarkernovel markerpathophysiologypathwaypreventpreventingrepositorysocial rolestomach emptyingtranscriptometranscriptome sequencingtranscriptomic sequencingtranscriptomicswhite blood cellwhite blood corpuscle
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Full Description

PROJECT SUMMARY/ABSTRACT
Similar to other complications of diabetes mellitus (DM), diabetic gastroenteropathy (DGE) reflects organ-

specific dysfunctions likely due to DM-related endocrine, metabolic and immune/inflammatory disturbances.

Therapies for DGE are ineffective and address the symptoms, not the disease itself. Hence, and aligned with

the mission of RFA-DK-20-030, this proposal seeks to uncover the cellular and molecular mechanisms of DGp

and its relative, non-ulcer dyspepsia, in carefully phenotyped patients. We focus on the links between

dysimmunity, ICC, glycemia, and mitochondrial dysfunction.

The specific aims are as follows: Aim 1. To analyze the relationship between the transcriptome and

epigenome of single gastric immune cells, gastric emptying (GE), and glycemia in DM and non-DM patients

with upper GI symptoms. Aim 2. To determine the relationship between the transcriptome and epigenome of

single circulating PBMCs and single gastric immune cells in DM and non-DM patients with upper GI symptoms.

Aim 3. To investigate the relationship between the transcriptome and epigenome of single gastric ICC and

immune cells and single circulating PBMCs in DM and non-DM patients with upper GI symptoms.

These studies will be investigated with in vivo (i.e., assessment of the DM phenotype, gastrointestinal

symptoms, and GE) followed by ex vivo assessments (i.e., transcriptome and epigenome of single circulating

PBMCs, single gastric CD45+ cells, and single ICC) in 45 patients undergoing sleeve gastrectomy (i.e., 15

patients in each of 3 groups: non-DM + normal GE, DM + normal GE, DM + delayed GE). This proposal is

anchored by, and builds on, an established bench-to-bedside collaboration between Drs. Bharucha and Ordog

which, through their complementary expertise, has enhanced our understanding of diabetic gastroparesis. It

seeks to better understand the pathogenesis, and through the studies in peripheral immune cells also identify

novel biomarkers, of DGE.

Grant Number: 5R01DK131455-05
NIH Institute/Center: NIH

Principal Investigator: ADIL BHARUCHA

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