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PRODUCTION OF MONOCYTE COLONY STIMULATING FACTOR BY HUMAN MELANOMA CELLS

PRODUCTION OF MONOCYTE COLONY STIMULATING FACTOR BY HUMAN MELANOMA CELLS
人黑色素瘤细胞产生单核细胞集落刺激因子
批准号:
3804760
负责人:
D S WEBB
金额:
$0.0万
依托单位:
--
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:
至

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中文摘要
翻译
在检测人类肿瘤细胞产生各种细胞因子时 株,我们发现测试的6个黑色素瘤细胞系中有6个 结构性产生M-CSF。在测试的5个细胞系中,这一点 产量相对较低(细胞融合时为1-5 ng/ml)。 而其中一株黑色素瘤细胞株RPMI5971释放了大约20- 多出100倍的M-CSF。在几个细胞系中,PMA的添加是 发现M-CSF的产量增加了10倍。此外,我们还有 初步证据表明,当M-CSF存在于足够高的浓度时 浓度,可能会抑制这些细胞的增殖。工作 目前正在研究通过这些细胞产生M-CSF的特性 并确定该细胞因子在黑色素瘤细胞系中是否起作用 调节这些细胞的生长。
英文摘要
While examining the production of various cytokines by human tumor cell lines, we have discovered that 6 of 6 melanoma cell lines tested constitutively produced M-CSF. In 5 of the cell lines tested, this production was relatively low (1-5 ng/ml when the cells were confluent) while 1 of the melanoma cell lines, RPMI 5971, released approximately 20- 100x more M-CSF. In several of the cell lines, the addition of PMA was found to increase M-CSF production 10-fold. In addition, we have preliminary evidence that M-CSF, when present in high enough concentrations, may act to inhibit the proliferation of these cells. Work is currently in progress to characterize the production of M-CSF by these melanoma cell lines and to determine if this cytokine plays a role in regulating the growth of these cells.
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REGULATION OF ADHESION MOLECULE EXPRESSION ON HUMAN MONOCYTES BY CYTOKINES
  • 批准号:
    3811207
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    D S WEBB
  • 依托单位:
    --
LFA-3, CD44, AND CD45--PHYSIOLOGIC TRIGGERS OF MONOCYTE TNF AND IL-1 RELEASE
  • 批准号:
    3811206
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    D S WEBB
  • 依托单位:
    --
ENHANCEMENT OF ICAM-1 SENSITIZES TUMOR CELLS TO MONOCYTE-MEDIATED LYSIS
  • 批准号:
    3804743
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    D S WEBB
  • 依托单位:
    --
LFA-3, CD44, AND CD45--PHYSIOLOGIC TRIGGERS OF MONOCYTE TNF AND IL-1 RELEASE
  • 批准号:
    3804742
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    D S WEBB
  • 依托单位:
    --
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