课题基金 / 基金详情

IMMUNOREGULATORY T CELL GLYCOPROTEINS: GENE CLONING

IMMUNOREGULATORY T CELL GLYCOPROTEINS: GENE CLONING
免疫调节 T 细胞糖蛋白:基因克隆
批准号:
3132272
负责人:
COLLEEN Elizabeth HAYES
金额:
$7.7万
依托单位国家:
美国
项目类别:
财政年份:
1985
资助国家:
美国
项目状态:
已结题
起止时间:
1985-02-01 至 1989-01-31

项目摘要

项目成果

COLLEEN Elizabeth HAYES的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Immunity protects animals from infectious diseases. Certain T lymphocytes regulate immunity in a highly-selective manner. These cells distinguish self tissue from foreign antigen. Membrane glycoproteins encoded by a gene cluster termed H-2 in the mouse occur on accessory cells and B lymphocytes with which regulatory T cells interact. These glycoproteins are involved in the process by which foreign antigen is rendered immunogenic, and thereby influence regulatory T cell induction. The molecular basis for immune regulation is not completely understood. Isolating and characterizing important immunoregulatory molecules has proven difficult. An alternative approach is to isolate the genes involved in regulating immunity by gene cloning. Proteins encoded by these genes can then be obtained in sufficient quantity to permit biochemical characterization and biological investigation. The specific aim of this proposal is to clone the genes encoding two important T lymphocyte membrane glycoproteins. Neither glycoprotein has been isolated from T cells and characterized biochemically. One, the I-J glycoprotein, demarcates a suppressive class of T lymphocytes responsible for impeding immunity. The other, I-At glycoprotein, characterizes and augmenting class of T lymphocytes responsible for enhancing immunity. The regulating activities of augmenting and suppressive T lymphocytes are antagonistic. Our preliminary results suggest that both glycoproteins participate in the process by which T cells distinguish foreign antigen; they may form part of a T cell receptor structure that binds antigen. We plan to achieve our goal by producing cell lines that biosynthesize significant quantities of the I-J and I-At glycoproteins. Messenger RNA derived from the cell lines will serve as a template for cDNA synthesis; cDNA will be cloned using an innovative scheme designed to facilitate eukaryotic gene expression in bacteria. Translated proteins will be detected immunochemically. Should this scheme prove unsuitable, alternative strategies are proposed.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
VITAMIN D COMPOUNDS FOR INFLAMMATORY BOWEL DISEASE
  • 批准号:
    6016975
  • 项目类别:
  • 资助金额:
    $16.98万
  • 财政年份:
    1999
  • 负责人:
    COLLEEN Elizabeth HAYES
  • 依托单位:
VITAMIN A INFLUENCE ON INTERFERON GAMMA GENE EXPRESSION
  • 批准号:
    2549275
  • 项目类别:
  • 资助金额:
    $10.23万
  • 财政年份:
    1993
  • 负责人:
    COLLEEN Elizabeth HAYES
  • 依托单位:
VITAMIN A INFLUENCE ON INTERFERON-GAMMA GENE EXPRESSION
  • 批准号:
    2146076
  • 项目类别:
  • 资助金额:
    $11.73万
  • 财政年份:
    1993
  • 负责人:
    COLLEEN Elizabeth HAYES
  • 依托单位:
VITAMIN A INFLUENCE ON INTERFERON-GAMMA GENE EXPRESSION
  • 批准号:
    2146077
  • 项目类别:
  • 资助金额:
    $12.19万
  • 财政年份:
    1993
  • 负责人:
    COLLEEN Elizabeth HAYES
  • 依托单位:
国内基金
海外基金
Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
  • 批准号:
    2022J011295
  • 项目类别:
    省市级项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2022
  • 负责人:
    王亚伟
  • 依托单位:
结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究