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DESCRIPTION (provided by applicant): Production of proinflammatory cytokines by macrophages significantly contributes to the pathogenesis of many inflammatory diseases including arthritis. Therefore, understanding the signaling mechanisms involved in the regulation of expression of pro-inflammatory molecules by macrophages is pivotal to developing drugs to combat inflammatory diseases. Recent studies have implicated Toll-like receptors (TLRs) in the initiation and maintenance of inflammation in a number of human diseases. Of particular importance is the role of TLR4, which critically regulates cytokine production and is therefore a drug target in inflammatory diseases. Hence, understanding the biochemical mechanisms by which TLR4-stimulated signaling pathways affect expression of inflammatory molecules is highly significant. Recent studies have demonstrated a critical role for non-visual arrestins (ARR2 and ARR3) in the regulation of TLR signaling and pathophysiology. Arrestins (ARRs) are scaffolding proteins originally discovered for their role in G- protein coupled receptor (GPCR) desensitization. Evidence indicates that ARR2 and 3 interact with distinct proteins and consequently regulate TLR4 signaling and inflammatory gene expression in macrophages and in vivo in mice. The objective of this application is to understand the biochemical mechanisms by which ARR2 and ARR3 regulate TLR4 signaling in macrophages and to test how this relates to inflammation in mice. To accomplish this objective, we will test the following hypotheses: (a) ARR2 and 3 play a crucial role in TLR4 signaling, and inflammatory mediator production in macrophages, and (b), this occurs via distinct protein-protein interactions, and (c) ARR2 and 3 are critically involved in TLR4-mediated inflammatory response in mice in vivo. Our studies should provide important insight into the mechanisms of TLR4 signaling in macrophages as well as provide potential therapeutic strategies for targeting TLR4 signaling in a variety of inflammatory diseases. PUBLIC HEALTH RELEVANCE: Toll-like receptor-4 activation in macrophages plays an important role in the development of various inflammatory diseases. Major objective of this application is to understand the regulation of TLR4-stimulated signaling pathways in macrophages and test as to how it relates to inflammatory diseases.
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GPCR Kinase-5 in Inflammatory Bowel Disease
  • 批准号:
    8511928
  • 项目类别:
  • 资助金额:
    $21.09万
  • 财政年份:
    2013
  • 负责人:
    Narayanan Parameswaran
  • 依托单位:
GPCR Kinase-2 in TNFalpha Signaling in Macrophages
  • 批准号:
    7860603
  • 项目类别:
  • 资助金额:
    $37.42万
  • 财政年份:
    2009
  • 负责人:
    Narayanan Parameswaran
  • 依托单位:
Arrestins in TLR4 Signaling in Macrophages
  • 批准号:
    7741415
  • 项目类别:
  • 资助金额:
    $29.91万
  • 财政年份:
    2009
  • 负责人:
    Narayanan Parameswaran
  • 依托单位:
GPCR Kinase-2 in TNFalpha Signaling in Macrophages
  • 批准号:
    7633012
  • 项目类别:
  • 资助金额:
    $37.51万
  • 财政年份:
    2009
  • 负责人:
    Narayanan Parameswaran
  • 依托单位:
国内基金
海外基金
AT1R-G蛋白/β-arrestins通路偏好性激活在急性肾损伤中的作用及其机制
  • 批准号:
    82104272
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    贾英丽
  • 依托单位:
催产素受体Gαq与β-arrestins偏爱型信号通路在产后抑郁症中的作用
  • 批准号:
    82104148
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    朱佳蕾
  • 依托单位:
β-arrestins在DC细胞迁移及自身免疫疾病中的作用及机制研究
  • 批准号:
    31871404
  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
    2018
  • 负责人:
    杜昌升
  • 依托单位:
β-arrestins调节小胶质细胞M1/M2表型转化及其在阿尔兹海默病进程中的作用
  • 批准号:
    81703488
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.1万元
  • 批准年份:
    2017
  • 负责人:
    方吟荃
  • 依托单位: