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PHAGOCYTE CYTOSKELETON-COMPLEMENT RECEPTOR INTERACTIONS

PHAGOCYTE CYTOSKELETON-COMPLEMENT RECEPTOR INTERACTIONS
吞噬细胞骨架-补体受体相互作用
批准号:
3142005
负责人:
GORDON D. ROSS
金额:
$18.94万
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-08-01 至 1992-07-31

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中文摘要
翻译
白细胞补体(C)系统由八种类型的膜C组成 受体、白细胞合成的各种C组分和血浆C 与白细胞相互作用的成分。 本项目的目标是 来表征白细胞C系统的功能。 具体目标 (1)检测淋巴细胞的体外免疫应答 并确定白细胞C系统是否在识别 旁路途径(AP)激活剂通过因子B裂解, 膜C5或因子H(H)与膜H受体(H-R)的结合, 表征CR对淋巴细胞活化的抑制2 (C3 d-受体)配体,并确定这是否代表一种机制, AP的非激活剂的歧视;(2)检查的作用, 白细胞C系统在巨噬细胞和自然 (3)确定是否血清或效应细胞来源的C3是 沉积在AP激活的肿瘤细胞上,以及这是否代表 效应细胞与肿瘤细胞结合重要机制 受体;(4)检查白细胞C系统在中性粒细胞中的作用 对酵母聚糖和细菌的呼吸爆发响应;以及(5)确定 无论是iC 3b还是特定的碳水化合物, 微生物细胞壁触发呼吸爆发, 溶酶体酶通过C受体3型(CR)识别3). (简体中文)
英文摘要
The leukocyte complement (C) system consists of eight types of membrane C receptors, various C components synthesized by leukocytes, and plasma C components that interact with leukocytes. The objective of this project is to characterize the function of the leukocyte C system. The specific aims are as follows: (1) examine the in vitro immune response of lymphocytes and determine if the leukocyte C system has a role in recognition of alternative pathway (AP) activators through either factor B cleavage of membrane C5 or the binding of factor H (H) to membrane H receptors (H-R), characterize the suppression of lymphocyte activation by CR2 (C3d-receptor) ligands and determine if this represents a mechanism for discrimination of nonactivators of the AP; (2) examine the role of the leukocyte C system in the tumoricidal activity of macrophages and natural killer cells; (3) determine whether serum-\or effector cell-derived C3 is deposited onto AP-activating tumor cells and whether this represents an important mechanism for effector cell binding to tumor cells by way of C receptors; (4) examine the role of the leukocyte C system in the neutrophil respiratory burst response to zymosan and bacteria; and (5) determine whether either iC3b or specific carbohydrates contained in the microorganism cell walls trigger a respiratory burst and release of lysosomal enzymes through recognition by C receptor type three (CR3). (CS)
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TARGETING OF PHAGOCYTE & NK CELL CR3 TO TUMOR-BOUND IC3B
  • 批准号:
    6407064
  • 项目类别:
  • 资助金额:
    $6.04万
  • 财政年份:
    2000
  • 负责人:
    GORDON D. ROSS
  • 依托单位:
TARGETING OF PHAGOCYTE & NK CELL CR3 TO TUMOR-BOUND IC3B
  • 批准号:
    6474779
  • 项目类别:
  • 资助金额:
    $11.42万
  • 财政年份:
    2000
  • 负责人:
    GORDON D. ROSS
  • 依托单位:
TARGETING OF PHAGOCYTE & NK CELL CR3 TO TUMOR-BOUND IC3B
  • 批准号:
    6134244
  • 项目类别:
  • 资助金额:
    $22.68万
  • 财政年份:
    2000
  • 负责人:
    GORDON D. ROSS
  • 依托单位:
TARGETING OF PHAGOCYTE & NK CELL CR3 TO TUMOR-BOUND IC3B
  • 批准号:
    6350447
  • 项目类别:
  • 资助金额:
    $25.92万
  • 财政年份:
    2000
  • 负责人:
    GORDON D. ROSS
  • 依托单位:
海外基金