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Extracellular cues that regulate gamma/delta lineage commitment and effector fat

Extracellular cues that regulate gamma/delta lineage commitment and effector fat
调节 γ/δ 谱系承诺和效应脂肪的细胞外信号
批准号:
9260751
负责人:
Juan Carlos Zuniga-Pflucker
金额:
$27.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:

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中文摘要
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英文摘要
T cells belonging to the yδ-lineage have been shown to serve a unique and critical role within the immune system. yδ T cells are widely distributed throughout mucosal and epithelial cell-rich tissues and are an important early source of IL-17 in response to a number of pathogens, recruiting granulocytes to the site of inflammation. However, how yδ T cells acquire the ability to respond as IL-17-producing cells prior to antigen exposure remains unclear. Additionally, how yδ T cells become specified and assigned to IL-17 or interferon-y (IFNy) effector fates remains to be fully elucidated. Recent evidence supports the notion that T cell receptor (TCR) signals affect the type of effector function that yδ T cells adopt within the thymus, such as becoming interferon-y (IFNy), IL-4 or IL-17 producing cells. Given the critical importance of Notch signaling throughout T cell differentiation, we hypothesized that the final differentiation and effector function selection by yδ T cells is guided by Notch receptor-ligand interactions, which influence the generation of IFNy vs. IL-17 producing cells. We will take advantage of the in vitro model system that we have previously established to elucidate the roles for TCR, Notch and cytokine signals in determining the final effector function of yδ T cells, and gain insight into the molecular basis for these selections by assembling global gene regulatory networks. Our aims are: 1) to address the role of Notch receptor signaling in yδ T cell effector differentiation; 2) to address the role of cytokine receptor signaling in yδ T cell effector differentiation; and, 3) to determine the role of E-proteins, together with Notch and cytokine signals, in specifying yδ T cell effector function. Taken together, our joint experimental approach and findings will provide important insights into the molecular processes controlling yδ T cell development and function, which would not be possible without the combined expertise provided by all members of this program.
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Distinct functions of E protein family members in regulating γδ T lineage commitment and effector fate
  • 批准号:
    10226998
  • 项目类别:
  • 资助金额:
    $30.97万
  • 财政年份:
    2014
  • 负责人:
    Juan Carlos Zuniga-Pflucker
  • 依托单位:
Distinct functions of E protein family members in regulating γδ T lineage commitment and effector fate
  • 批准号:
    10462549
  • 项目类别:
  • 资助金额:
    $30.74万
  • 财政年份:
    2014
  • 负责人:
    Juan Carlos Zuniga-Pflucker
  • 依托单位:
Distinct functions of E protein family members in regulating γδ T lineage commitment and effector fate
  • 批准号:
    10685630
  • 项目类别:
  • 资助金额:
    $30.35万
  • 财政年份:
    2014
  • 负责人:
    Juan Carlos Zuniga-Pflucker
  • 依托单位:
Extracellular cues that regulate gamma/delta lineage commitment and effector fat
  • 批准号:
    8608278
  • 项目类别:
  • 资助金额:
    $35.04万
  • 财政年份:
    2014
  • 负责人:
    Juan Carlos Zuniga-Pflucker
  • 依托单位:
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