Evans C H, Heinbaugh J A
Immunopharmacology. 1981 Dec;3(4):347-59. doi: 10.1016/0162-3109(81)90027-8.
Guinea pig lymphotoxin inhibits the growth of mouse alpha L929 and guinea pig 104C1 tumor cells with lethal doses (LD 50's) of 0.4 and 200 units lymphotoxin/ml, respectively, in a colony inhibition assay. Refeeding with lymphotoxin-free medium is followed by resumption of 104C1 but not alpha L929 cell growth. This suggests that growth inhibition of alpha L929 is primarily due to cytolytic mechanisms, while that of 104C1 cells is due to cytostatic mechanisms. This is confirmed by radionuclide (3H, 51Cr, and 75Se) release assays with LD 50's of 1.0, 1.9, and 2.4 units lymphotoxin/ml, respectively, for alpha L929 cells, whereas as many as 100 units lymphotoxin/ml produce no radionuclide release from 104C1 cells. The L cell variant L929M is 10-fold more resistant to lymphotoxin colony inhibitory activity and 40-300-fold more resistant to cytolytic lymphotoxin activity as measured by the three radionuclide release assays than are alpha L929 cells. L929 and 2071 L cell variants are more resistant as a result of smaller cytolytic and cytostatic responses and some tumor cells, such as one strain of L1210 mouse leukemia cells, exhibit no detectable cytolytic or cytostatic responses to 100 units of guinea pig lymphotoxin. These observations demonstrate that the divergent susceptibilities of different cells to lymphotoxin result in part from constitutive variations in cellular cytolytic and reversible cytostatic responses to lymphotoxin.
在集落抑制试验中,豚鼠淋巴毒素分别以0.4和200单位淋巴毒素/毫升的致死剂量(LD50)抑制小鼠α-L929和豚鼠104C1肿瘤细胞的生长。用不含淋巴毒素的培养基重新培养后,104C1细胞恢复生长,而α-L929细胞则不然。这表明α-L929细胞的生长抑制主要是由于细胞溶解机制,而104C1细胞的生长抑制是由于细胞静止机制。放射性核素(3H、51Cr和75Se)释放试验证实了这一点,α-L929细胞的LD50分别为1.0、1.9和2.4单位淋巴毒素/毫升,而高达100单位淋巴毒素/毫升的剂量也不会使104C1细胞释放放射性核素。L细胞变体L929M对淋巴毒素集落抑制活性的抗性比α-L929细胞高10倍,对细胞溶解淋巴毒素活性的抗性比α-L929细胞高40至300倍,这是通过三种放射性核素释放试验测得的。L929和2071 L细胞变体由于细胞溶解和细胞静止反应较小而更具抗性,一些肿瘤细胞,如一种L12C10小鼠白血病细胞株,对100单位豚鼠淋巴毒素未表现出可检测到的细胞溶解或细胞静止反应。这些观察结果表明,不同细胞对淋巴毒素的不同敏感性部分源于细胞对淋巴毒素的细胞溶解和可逆细胞静止反应的组成性差异。