Tanaka M
Nagoya National Hospital, Hematological Disease Center, Japan.
Thromb Res. 1989 Oct 15;56(2):201-11. doi: 10.1016/0049-3848(89)90162-x.
Cell lysates of the human monoblastic leukemia cell line, THP-1, have procoagulant activity (PCA) that is Ca++-dependent and not demonstrable in either Factor VII-, or Factor X-deficient plasma. The PCA of THP-1 cells was enhanced by human recombinant tumor necrosis factor-alpha (TNF-alpha) up to five fold. There was a dose-dependent increase in PCA when THP-1 cells were cultured with concentrations of TNF-alpha, up to 10 U/ml. PCA of cell lysates or whole cell preparations was measured in comparison to a rabbit brain thromboplastin standard. The effect of TNF-alpha was enhanced by recombinant human interferon-gamma (IFN-gamma). Cycloheximide inhibited the induction of PCA by THP-1 cells, which shows that the protein synthesis is essential to mediate the effect of TNF-alpha. THP-1 cells and U937 cells bound 125I-labeled TNF specifically. The numbers of receptors per cell were found to be 1,890 and 1,550 for THP-1 and U937 cells, respectively. Other lymphoid and myeloblastic leukemia cell lines examined did not have TNF receptors, indicating that the effect of TNF-alpha is mediated by the receptors on the cell surface.
人单核细胞白血病细胞系THP - 1的细胞裂解物具有促凝血活性(PCA),该活性依赖于Ca++,且在因子VII或因子X缺乏的血浆中无法检测到。人重组肿瘤坏死因子-α(TNF-α)可使THP - 1细胞的PCA增强达五倍。当THP - 1细胞与浓度高达10 U/ml的TNF-α一起培养时,PCA呈剂量依赖性增加。与兔脑凝血活酶标准品相比,测量了细胞裂解物或全细胞制剂的PCA。重组人干扰素-γ(IFN-γ)增强了TNF-α的作用。放线菌酮抑制THP - 1细胞诱导PCA,这表明蛋白质合成对于介导TNF-α的作用至关重要。THP - 1细胞和U937细胞特异性结合125I标记的TNF。发现THP - 1细胞和U937细胞每细胞的受体数量分别为1890和1550。所检测的其他淋巴细胞和髓母细胞白血病细胞系没有TNF受体,这表明TNF-α的作用是由细胞表面的受体介导的。