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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
O-连接的 N-乙酰氨基葡萄糖稳态在胰腺 β 细胞发育和功能中的作用
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

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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.
期刊论文(19)
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会议论文
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
12
    Nutrient-sensor O-GlcNAc Transferase Regulation of Autophagy in Homeostatis of Pancreatic Beta-cell Mass and Function
    • 批准号:
      10907874
    • 项目类别:
    • 资助金额:
      $23.25万
    • 财政年份:
      2023
    • 负责人:
      Emilyn Alejandro
    • 依托单位:
    Placental Insulin Signaling and mTOR Nutrient-Sensing Programming of Offspring Metabolic Health
    • 批准号:
      10679756
    • 项目类别:
    • 资助金额:
      $54.0万
    • 财政年份:
      2023
    • 负责人:
      Emilyn Alejandro
    • 依托单位:
    Placental Insulin Signaling and mTOR Nutrient-Sensing Programming of Offspring Metabolic Health
    • 批准号:
      10625938
    • 项目类别:
    • 资助金额:
      $9.3万
    • 财政年份:
      2022
    • 负责人:
      Emilyn Alejandro
    • 依托单位:
    Innate Immune Complement System and Developmental Programming of Functional β Cell Mass
    • 批准号:
      10194574
    • 项目类别:
    • 资助金额:
      $19.36万
    • 财政年份:
      2020
    • 负责人:
      Emilyn Alejandro
    • 依托单位:
    海外基金