The role of O-linked N-Acetylglucosamine Homeostasis in Pancreatic Beta-cell Development and Function
The role of O-linked N-Acetylglucosamine Homeostasis in Pancreatic Beta-cell Development and Function
批准号:
10406255
负责人:
Emilyn Alejandro
金额:
$38.5万
依托单位:
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:
2018-07-01 至 2024-05-31
关键词:
AblationAffectAmericanApoptosisB cell differentiationB-Cell DevelopmentBeta CellBiologicalBirthCause of DeathCell MaintenanceCellsCellular Metabolic ProcessCellular biologyChronic DiseaseClinical TreatmentCuesDataDefectDevelopmentDiabetes MellitusDown-RegulationEmbryoEndocrineEnzymesFunctional disorderGoalsGolgi ApparatusGrantGrowthHealthHigh Fat DietHomeostasisHormonalHumanIndividualInsulinIslet CellLeadLifeLinkMaintenanceMass Spectrum AnalysisMetabolicMetabolic stressModelingModificationMolecularMolecular TargetMusMutateMutationNon-Insulin-Dependent Diabetes MellitusNutrientO-GlcNAc transferasePancreasPathway interactionsPatientsPhenotypePost-Translational Protein ProcessingPredispositionPropertyProteinsRegulationReportingRoleSignal TransductionSignaling ProteinSiteStressStructure of beta Cell of isletTestingTimeUnited StatesWild Type Mousebiological adaptation to stresscell growthearly onsetendocrine pancreas developmentendoplasmic reticulum stressexhaustgenome wide association studyglucose metabolismglycosylationhomeodomainimprovedinsulin secretioninsulin signalingisletoverexpressionpancreas developmentpeptide O-linked N-acetylglucosamine-beta-N-acetylglucosaminidaseprogenitorresponseself-renewalsensortranscription factor
中文摘要
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英文摘要
Type 2 diabetes (T2D) is the most common chronic disease affecting human health. Recent longitudinal and genome-wide association studies provide strong evidence that the ability of pancreatic β-cells to fulfill insulin demand through development, growth, survival, and function is a key determinant of whether an individual will develop T2D ! under various nutrient conditions. However, there are no effective clinical treatments that target β-cell growth and maintenance of their differentiated identity as insulin producing-cells. We propose that OGT (O-GlcNAc Transferase), a nutrient-sensor expressed at a very high level in β-cells, has key developmental regulatory properties and the ability to integrate signaling networks to regulate β-cell plasticity in response to insulin demand and nutrient stress. OGT is the sole enzyme adding a single O-GlcNAc post-translational modification (O-GlcNAcylation) onto proteins to orchestrate and fine-tune glucose metabolism, and β-cell growth and maintenance of identity under stress responses to nutrient changes and hormonal cues. We hypothesize that OGT tightly controls the O-GlcNAcylation state of downstream targets, including Pdx1, to promote β-cell development and function. Thus, our long-term goal is to define the mechanisms of how OGT integrates signaling networks impinging on β-cell plasticity (development and identity) to promote functional β-cells. We will test our hypothesis with the following Aims: 1. To establish the molecular mechanisms of how OGT regulates β-cell development and mass. 2. To delineate the mechanisms of how OGT regulates β-cell mass and identity under metabolic stress. The impact of this grant will show the central role of OGT in β-cell development and mass maintenance, and illustrate the translational relevance of OGT during time windows critical to metabolic health . Finally, these results will advance the field of β-cell biology and will open new horizons for therapies for patients with diabetes.
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DOI:
10.3390/cells10102801
发表时间:
2021-10-19
期刊:
Cells
影响因子:
6
作者:
[Mohan R, Jo S, Da Sol Chung E, Oribamise E, Lockridge A, Abrahante-Lloréns JE, Ruan HB, Yang XY, Alejandro EU]
通讯作者:
Alejandro EU
DOI:
10.1530/jme-18-0059
发表时间:
2019-02-01
期刊:
Journal of molecular endocrinology
影响因子:
3.5
作者:
[Hart B, Morgan E, Alejandro EU]
通讯作者:
Alejandro EU
DOI:
10.1016/j.jbc.2021.100297
发表时间:
2021-01
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Essawy A, Jo S, Beetch M, Lockridge A, Gustafson E, Alejandro EU]
通讯作者:
Alejandro EU
DOI:
10.3390/ijms22136918
发表时间:
2021-06-28
期刊:
International journal of molecular sciences
影响因子:
5.6
作者:
[Moore M, Avula N, Jo S, Beetch M, Alejandro EU]
通讯作者:
Alejandro EU
DOI:
10.1530/joe-23-0069
发表时间:
2023-12-01
期刊:
JOURNAL OF ENDOCRINOLOGY
影响因子:
4
作者:
[Jo, Seokwon, Alejandro, Emilyn U.]
通讯作者:
Alejandro, Emilyn U.
共 12 条
Nutrient-sensor O-GlcNAc Transferase Regulation of Autophagy in Homeostatis of Pancreatic Beta-cell Mass and Function
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批准号:10907874
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项目类别:
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资助金额:$23.25万
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财政年份:2023
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负责人:Emilyn Alejandro
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依托单位:
Placental Insulin Signaling and mTOR Nutrient-Sensing Programming of Offspring Metabolic Health
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批准号:10679756
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资助金额:$54.0万
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财政年份:2023
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负责人:Emilyn Alejandro
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依托单位:
Placental Insulin Signaling and mTOR Nutrient-Sensing Programming of Offspring Metabolic Health
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批准号:10625938
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项目类别:
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资助金额:$9.3万
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财政年份:2022
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负责人:Emilyn Alejandro
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Innate Immune Complement System and Developmental Programming of Functional β Cell Mass
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批准号:10194574
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资助金额:$19.36万
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财政年份:2020
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负责人:Emilyn Alejandro
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依托单位:
The role of O-linked N-Acetylglucosamine Homeostasis in Pancreatic Beta-cell Development and Function
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批准号:10158468
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项目类别:
-
资助金额:$38.5万
-
财政年份:2018
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负责人:Emilyn Alejandro
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依托单位:
The role of O-linked N-Acetylglucosamine Homeostasis in Pancreatic Beta-cell Development and Function
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批准号:9922900
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项目类别:
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资助金额:$38.5万
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财政年份:2018
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负责人:Emilyn Alejandro
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依托单位:
O-linked-N-acetylglucosamine Post-translational Modification in Pancreatic Beta-cells Regulating ER Stress and Mitochondrial Function
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批准号:9387765
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项目类别:
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资助金额:$19.15万
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财政年份:2017
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负责人:Emilyn Alejandro
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依托单位:
Mechanisms of Developmental Programing of beta-cell Susceptibility to Glucolipotoxicity
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批准号:9285779
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项目类别:
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资助金额:$15.12万
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财政年份:2014
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负责人:Emilyn Alejandro
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依托单位:
Mechanisms of Developmental Programing of beta-cell Susceptibility to Glucolipotoxicity
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批准号:8804376
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项目类别:
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资助金额:$13.39万
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财政年份:2014
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负责人:Emilyn Alejandro
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依托单位:
Mechanisms of Developmental Programing of beta-cell Susceptibility to Glucolipotoxicity
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批准号:9176214
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项目类别:
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资助金额:$12.28万
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财政年份:2014
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负责人:Emilyn Alejandro
-
依托单位:
Mechanisms of Developmental Programing of beta-cell Susceptibility to Glucolipotoxicity
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批准号:9507001
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项目类别:
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资助金额:$0.14万
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财政年份:2014
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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批准号:7907023
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项目类别:
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资助金额:$0.42万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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批准号:7323709
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项目类别:
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资助金额:$2.12万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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批准号:7475370
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项目类别:
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资助金额:$0.79万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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批准号:7486173
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项目类别:
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资助金额:$2.15万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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批准号:7664649
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项目类别:
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资助金额:$0.42万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
Anti-apoptotic role of raf-1 in beta-cell insulin signaling
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项目类别:
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资助金额:$2.31万
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财政年份:2007
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负责人:Emilyn Alejandro
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依托单位:
海外基金