Matthews N
Immunology. 1981 Sep;44(1):135-42.
Human monocytes incubated in vitro for 20 hr at 37 degrees release a factor which is cytotoxic to a number of human and murine tumour cell lines: untransformed cells appear to be less susceptible. A similar factor is produced under comparable conditions by myelomonocytic leukaemic cells and by macrophages derived from monocytes by in vitro culture for 8 days. Maximum production of the factor occurred in the presence of foetal calf serum or autologous plasma and endotoxin. The factor is newly synthesized in culture as its production is reduced if the monocytes are treated with cycloheximide or actinomycin D or incubated at lower temperatures. Freshly isolated monocytes do not release the factor on freeze--thaw or hypotonic lysis. The monocyte cytotoxin has apparent molecular weights of 34,000 on Ultrogel AcA54 gel filtration and 140,000 on gradient polyacrylamide gel electrophoresis; it has beta 2--gamma 1 electrophoretic mobility in polyacrylamide gel and does not appear to be C3a or arginase.
人单核细胞在37℃体外培养20小时后释放出一种对多种人及鼠肿瘤细胞系具有细胞毒性的因子:未转化的细胞似乎较不易感。在类似条件下,骨髓单核细胞白血病细胞以及通过体外培养8天从单核细胞衍生而来的巨噬细胞也会产生类似因子。该因子在胎牛血清、自体血浆和内毒素存在的情况下产量最高。该因子是在培养过程中新合成的,因为如果用环己酰亚胺或放线菌素D处理单核细胞或在较低温度下培养,其产量会降低。刚分离的单核细胞经冻融或低渗裂解后不会释放该因子。单核细胞细胞毒素在Ultrogel AcA54凝胶过滤中的表观分子量为34,000,在梯度聚丙烯酰胺凝胶电泳中的表观分子量为140,000;它在聚丙烯酰胺凝胶中具有β2-γ1电泳迁移率,似乎不是C3a或精氨酸酶。