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DESCRIPTION (provided by applicant): My goal as a physician-scientist is to improve the lives of children through research on the pathophysiology of diabetes mellitus. To this end I have spent the past several years training in the laboratory of Dr Morris White investigating the etiology of beta-cell dysfunction in diabetes. This proposal will allow me to further train in cell biology and physiology as I transition to a career as an independently funded investigator in the Joslin Diabetes Center. Little is known about the regulation of beta-cell proliferation, although the insulin-like growth factors (IGFs), other growth factors, and the pancreatic transcription factor Pdx1 may play a role. Insulin Receptor Substrate (IRS)-2 related pathways are essential for beta-cell survival: Irs2 knockout (-/-) mice develop beta-cell failure and insulin resistance resulting in death from diabetes. I have previously shown that Irs2 signaling alters levels of Pdx1, a pancreatic transcription factor that promotes beta-cell mass and function. I also found that Pdx1 overexpression can stimulate beta-cell proliferation in mice, as measured by BrdU incorporation into beta-cells. In most tissues mitogenic stimuli increase gene expression of G1 cyclin D-type cyclins, which partner with cyclin dependent kinase (cdk)-4 or -6 to promote cell growth. Remarkably, cdk4-/- mice develop diabetes from inadequate beta-cell growth. From these findings I suspected that one of the D-type cyclins might be an important partner of cdk4 in islet expansion. Supporting this notion I have recently found that cyclin D2-/- mice develop diabetes with impaired beta-cell growth. Further experiments suggest that Pdx1 could regulate beta-cell proliferation by directly binding to the cyclin D2 promoter. This proposal will test the hypothesis that cyclin D2 is essential for normal islet growth and that Pdx1 regulates beta-cell proliferation by regulating cyclin D2 activity by examining the following specific aims: 1. To test if cyclin D2 is an essential regulator of islet growth. 2. To test if Pdx1 influences beta-cell proliferation by regulating cyclin D2.
期刊论文(7)
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会议论文
Development. Esophageal stem cells, where art thou?
发展。食管干细胞,您在哪里?
DOI: 10.1126/science.1227506
发表时间: 2012-08-31
期刊: Science (New York, N.Y.)
影响因子: --
作者: [Kushner JA]
通讯作者: Kushner JA
DOI: 10.2337/db12-0848
发表时间: 2013-05
期刊: Diabetes
影响因子: 7.7
作者: [Rankin MM, Wilbur CJ, Rak K, Shields EJ, Granger A, Kushner JA]
通讯作者: Kushner JA
Cell Lineage and Homeostasis of Pancreatic Beta Cells in the Aged
  • 批准号:
    8164359
  • 项目类别:
  • 资助金额:
    $35.39万
  • 财政年份:
    2011
  • 负责人:
    JAKE ALDEN KUSHNER
  • 依托单位:
Cell Lineage and Homeostasis of Pancreatic Beta Cells in the Aged
  • 批准号:
    8321469
  • 项目类别:
  • 资助金额:
    $34.88万
  • 财政年份:
    2011
  • 负责人:
    JAKE ALDEN KUSHNER
  • 依托单位:
Cell Lineage and Homeostasis of Pancreatic Beta Cells in the Aged
  • 批准号:
    8868872
  • 项目类别:
  • 资助金额:
    $32.34万
  • 财政年份:
    2011
  • 负责人:
    JAKE ALDEN KUSHNER
  • 依托单位:
Cell Lineage and Homeostasis of Pancreatic Beta Cells in the Aged
  • 批准号:
    8529428
  • 项目类别:
  • 资助金额:
    $32.48万
  • 财政年份:
    2011
  • 负责人:
    JAKE ALDEN KUSHNER
  • 依托单位:
国内基金
海外基金
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
  • 批准号:
    32170319
  • 项目类别:
    面上项目
  • 资助金额:
    58.00万元
  • 批准年份:
    2021
  • 负责人:
    董春海
  • 依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
  • 批准号:
    --
  • 项目类别:
    --
  • 资助金额:
    58万元
  • 批准年份:
    2021
  • 负责人:
    董春海
  • 依托单位:
ID1 (Inhibitor of DNA binding 1) 在口蹄疫病毒感染中作用机制的研究
番茄EIN3-binding F-box蛋白2超表达诱导单性结实和果实成熟异常的机制研究
  • 批准号:
    31372080
  • 项目类别:
    面上项目
  • 资助金额:
    80.0万元
  • 批准年份:
    2013
  • 负责人:
    杨迎伍
  • 依托单位: