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Regulation of CXCR4 Signaling

Regulation of CXCR4 Signaling
CXCR4 信号传导的调节
批准号:
7303450
负责人:
Jeffrey L Benovic
金额:
$29.45万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-11 至 2012-05-31

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DESCRIPTION (provided by applicant): The chemokine receptor CXCR4 is an essential GPCR that has been implicated in a number of human diseases including HIV, WHIM syndrome, and cancer. The detailed mechanisms involved in the regulation of CXCR4 function and its role in cancer are currently poorly understood. Agonist- dependent signaling of GPCRs is principally regulated by GPCR kinases (GRKs) and arrestins with GRK phosphorylation of an activated GPCR often being the initial step in the regulatory process. CXCR4 is rapidly phosphorylated following agonist activation, although the specific sites of phosphorylation, the kinases involved, and the functional roles are not well defined. In this application, we propose to use molecular, biochemical, and cellular strategies to better characterize the mechanisms that regulate CXCR4 expression and function in normal and cancer cells. Our initial studies suggest that GRKS may play the major role in agonist-specific phosphorylation of CXCR4 in HEK293 cells. In addition, enhanced Ca2+ mobilization is observed when GRKS, GRK6, arrestin-2, or arrestin-3 are knocked down while ERK1/2 activation is enhanced by the loss of GRK2 but decreased by the loss of GRKS, GRK6, arrestin-2, or arrestin-3. These initial studies suggest that GRKs and arrestins may differentially regulate CXCR4 signaling. We will test the hypothesis that site-specific phosphorylation of CXCR4 mediates the kinetics and specificity of signaling by addressing several important questions. What specific residues in CXCR4 are phosphorylated in response to agonist stimulation and what kinases mediate site-specific phosphorylation? What are the functional roles of CXCR4 phosphorylation and what mechanisms underlie the functional effects of site-specific phosphorylation? Are any of these mechanisms dysfunctional in cancer? Our studies should provide important insight into the mechanisms involved in CXCR4 regulation as well as provide potential therapeutic approaches for controlling CXCR4 function.
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Training Grant in Cellular, Biochemical and Molecular Sciences
  • 批准号:
    10655637
  • 项目类别:
  • 资助金额:
    $42.44万
  • 财政年份:
    2022
  • 负责人:
    Jeffrey L Benovic
  • 依托单位:
Structural and dynamic analysis of GRK interaction with G protein-coupled receptors
  • 批准号:
    9913308
  • 项目类别:
  • 资助金额:
    $52.91万
  • 财政年份:
    2018
  • 负责人:
    Jeffrey L Benovic
  • 依托单位:
Regulation of G protein-coupled receptor signaling and trafficking
  • 批准号:
    10214632
  • 项目类别:
  • 资助金额:
    $50.7万
  • 财政年份:
    2017
  • 负责人:
    Jeffrey L Benovic
  • 依托单位:
Regulation of G protein-coupled receptor signaling and trafficking
  • 批准号:
    9978885
  • 项目类别:
  • 资助金额:
    $50.7万
  • 财政年份:
    2017
  • 负责人:
    Jeffrey L Benovic
  • 依托单位:
海外基金