课题基金 / 基金详情

项目摘要

项目成果

SANDEEP Kumar TRIPATHY的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):自然杀伤(NK)细胞是通过释放细胞溶解颗粒或免疫刺激细胞因子来破坏异常细胞(病毒感染或恶性细胞)的淋巴细胞。NK细胞在其细胞表面同时表达激活受体和抑制受体。据信,激活和抑制受体的信号平衡调节NK细胞。NK细胞发展其受体库的机制现在开始被理解。我们的实验室最近证明NK细胞上的抑制性Ly49受体与其MHC I类配体在发育早期的相互作用是NK细胞功能成熟的原因(称为“许可”)。这一事件可能发生在骨髓中NK细胞成熟的过程中。在缺乏“许可”的情况下,NK细胞无法进行稳健的免疫活动。免疫系统受到靶细胞刺激后的免疫反应。另一方面,关于激活受体在NK细胞发育中的作用知之甚少。Ly49H受体是一种激活受体,在某些小鼠品系的NK细胞表面表达,它赋予小鼠巨细胞病毒(MCMV)感染的抵抗力。最近,该受体的配体被鉴定为mcmv编码的蛋白m157。核心假设是m157的组成性表达会改变Ly49H+ NK细胞的发育和/或功能。本提案的目标是通过三个具体目标来检验这一假设。Aim 1的研究将确定m157(一种病毒编码蛋白)的表达是否会在缺乏Ly49H的情况下改变NK细胞的发育。这将通过在不表达Ly49H受体的菌株中产生表达m157的转基因小鼠来实现。在Aim2中的研究将确定在Ly49H存在下m157的表达是否会改变NK细胞的发育。这将通过在Aim 1中产生的小鼠与表达Ly49H的小鼠株交配来完成。Aim 3的研究将确定骨髓外m157的表达是否通过以肝脏特异性或肠道特异性方式表达m157来改变NK细胞的发育和/或功能。自然杀伤细胞(NK)在病毒和肿瘤的免疫应答中起着重要作用。对NK细胞发育的深入了解可能会导致基于NK细胞的新型疗法的产生,这些疗法可能被证明对病毒感染和癌症的治疗有用。
英文摘要
DESCRIPTION (provided by applicant): Natural killer (NK) cells are lymphocytes that destroy abnormal cells (virus infected or malignant cells) through the release of cytolytic granules or immune stimulatory cytokines. NK cells express both activating and inhibitory receptors on their cell surface. It is believed that a balance of signaling from both activating and inhibitory receptors regulates the NK cell. The mechanism by which NK cells develop their repertoire of receptors is now beginning to be understood. Our laboratory has recently demonstrated that the interaction of inhibitory Ly49 receptors on NK cells with their MHC class I ligands early in development is responsible for functional maturation of NK cells (termed "licensing"). This event likely takes place as the NK cell matures in the bone marrow. In the absence of "licensing", the NK cell fails to carry out a robust.immune responses upon stimulation by a target cell. On the other hand, little is known about the role of activating receptors in NK cell development. The Ly49H receptor is an activating receptor, expressed on the surface of NK cells in certain strains of mice, which confers resistance to murine cytomegalovirus (MCMV) infection. Recently, the ligand for this receptor has been identified as the MCMV-encoded protein m157. The core hypothesis is that the constitutive expression of m157 will alter the development and/or function of Ly49H+ NK cells. The goal of this proposal is to test this hypothesis via three specific aims. The studies in Aim 1 will determine if the expression of m157, a viral-encoded protein, will alter the development of NK cells in the absence of Ly49H. This will be accomplished by generating an m157-expressing transgenic mouse in a strain that does not express the Ly49H receptor. The studies in Aim2 will determine if expression of m157 in the presence of Ly49H will alter NK cell development. This will be accomplished by mating the mouse generated in Aim 1 with a strain of mouse that expresses Ly49H. The studies in Aim 3 will determine if the expression of m157 outside of the bone marrow alters NK cell development and/or function by expressing ml 57 in a liver-specific or intestine-specific fashion. Natural killer (NK) cells play an important role in the immune response to viruses and tumors. Insight into the development of NK cells could result in the generation of novel NK cell-based therapies that may prove useful in the treatment of viral infection and cancers.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
MECHANISMS OF NATURAL KILLER CELL TOLERANCE
  • 批准号:
    8306743
  • 项目类别:
  • 资助金额:
    $38.0万
  • 财政年份:
    2011
  • 负责人:
    SANDEEP Kumar TRIPATHY
  • 依托单位:
MECHANISMS OF NATURAL KILLER CELL TOLERANCE
  • 批准号:
    8481509
  • 项目类别:
  • 资助金额:
    $35.72万
  • 财政年份:
    2011
  • 负责人:
    SANDEEP Kumar TRIPATHY
  • 依托单位:
MECHANISMS OF NATURAL KILLER CELL TOLERANCE
  • 批准号:
    8680002
  • 项目类别:
  • 资助金额:
    $38.0万
  • 财政年份:
    2011
  • 负责人:
    SANDEEP Kumar TRIPATHY
  • 依托单位:
MECHANISMS OF NATURAL KILLER CELL TOLERANCE
  • 批准号:
    8186484
  • 项目类别:
  • 资助金额:
    $38.0万
  • 财政年份:
    2011
  • 负责人:
    SANDEEP Kumar TRIPATHY
  • 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: