Laskov R, Lancz G, Ruddle N H, McGrath K M, Specter S, Klein T, Djeu J Y, Friedman H
Hubert H. Humphrey Center for Experimental Medicine and Cancer Research, Hebrew University, Jerusalem, Israel.
J Immunol. 1990 May 1;144(9):3424-30.
Media from murine pre-B and B lymphoma cell cultures, but not from myeloma cell cultures, was cytotoxic to WEHI 164 cells, causing these TNF-sensitive targets to release 51Cr. The cytotoxic activity in the culture medium reached maximum levels approximately 4 days after the cell culture was initiated. The constitutive production of the factors was not influenced by depletion of serum from the medium or by the addition of either phorbol ester or bacterial endotoxin. The factor has a Mr greater than 10 kDa, and its cytotoxicity was abolished by anti-serum against murine TNF. Northern blot analysis with the use of cDNA probes to murine tumor necrosis factor (TNF-alpha) and lymphotoxin (LT, TNF-beta) showed high levels of TNF-mRNA in the pre-B cell lines, lower levels in the mature B cell lines and no TNF-mRNA in the myeloma cell lines. LT mRNA was present in pre-B cell lines, at a much lower concentration in only one of the B cell lines, and was not present in three other B lymphomas or in the myelomas tested. The results show a positive correlation between the presence of TNF and/or LT mRNA and the 51Cr-releasing activity present in the cell culture medium. Our data indicate that TNF and LT can be produced by murine B cells and that the synthesis of these cytokines may be restricted to certain differentiation stages of the B cell lineage.
来自小鼠前B细胞和B淋巴瘤细胞培养物的培养基,而非骨髓瘤细胞培养物的培养基,对WEHI 164细胞具有细胞毒性,使这些对肿瘤坏死因子(TNF)敏感的靶细胞释放51Cr。细胞培养开始后约4天,培养基中的细胞毒性活性达到最高水平。这些因子的组成性产生不受培养基中血清耗竭的影响,也不受佛波酯或细菌内毒素添加的影响。该因子的分子量大于10 kDa,其细胞毒性被抗小鼠TNF血清消除。使用针对小鼠肿瘤坏死因子(TNF-α)和淋巴毒素(LT,TNF-β)的cDNA探针进行的Northern印迹分析显示,前B细胞系中TNF-mRNA水平较高,成熟B细胞系中水平较低,骨髓瘤细胞系中无TNF-mRNA。LT mRNA在前B细胞系中存在,仅在一个B细胞系中浓度低得多,在其他三个B淋巴瘤或所测试的骨髓瘤中不存在。结果显示TNF和/或LT mRNA的存在与细胞培养基中存在的51Cr释放活性之间呈正相关。我们的数据表明,TNF和LT可由小鼠B细胞产生,并且这些细胞因子的合成可能仅限于B细胞谱系的某些分化阶段。