Bersani L, Colotta F, Ghezzi P, Mantovani A
Immunol Lett. 1985;11(5-6):351-5. doi: 10.1016/0165-2478(85)90119-1.
Human monocytes kill Actinomycin D-treated WEHI 164 sarcoma cells in a 6 h 51Cr release assay (drug dependent cellular cytotoxicity, DDCC). In the present study we have investigated and characterized the human monocyte production of a cytotoxic factor which mediates DDCC. Cell-free supernatants obtained culturing monocytes for 4-5 h kill Actinomycin D-treated WEHI 164 cells but not untreated tumor cells. A series of antiproteases inhibits the cytotoxic activity of cell-free monocyte supernatants, whereas scavengers of reactive oxygen intermediates were ineffective. The lytic activity was destroyed treating supernatants at 100 degrees C for 5 min or by exposure to acid pH or to proteinase K, whereas it was unaffected by heating at 56 degrees C for 30 min. Upon gel filtration on Sephacryl S200, cytolytic activity eluted in the 33,000 molecular weight range.
在一项6小时的51铬释放试验(药物依赖性细胞毒性,DDCC)中,人单核细胞可杀死经放线菌素D处理的WEHI 164肉瘤细胞。在本研究中,我们对介导DDCC的细胞毒性因子的人单核细胞产生进行了研究和表征。培养单核细胞4 - 5小时获得的无细胞上清液可杀死经放线菌素D处理的WEHI 164细胞,但不能杀死未处理的肿瘤细胞。一系列抗蛋白酶可抑制无细胞单核细胞上清液的细胞毒性活性,而活性氧中间体清除剂则无效。将上清液在100℃处理5分钟、暴露于酸性pH值或蛋白酶K中可破坏其裂解活性,而在56℃加热30分钟则对其无影响。在Sephacryl S200上进行凝胶过滤时,细胞溶解活性在分子量33,000范围内洗脱。