Peters J H, Bessler W G, Schimmelpfeng L
Immunol Commun. 1979;8(4):425-33. doi: 10.3109/08820137909050056.
The sequence of events in mitogenic T-lymphocyte activation was investigated by employing purified mouse peritoneal adherent cells and T-lymphocyte populations. After treatment of adherent cells with the oxidizing agents sodium periodate or neuroaminidase plus galactose oxidase and removal of the mitogens, the cells acquired the ability to stimulate purified T-lymphocytes added subsequently. For this process of T-lymphocyte activation, the additional presence of the membrane interacting substances polyethylene glycol, dextran, nonmitogenic Helix pomatia agglutinin, or inactivated sendai virus was required. Lysates of mitogen-treated peritoneal adherent cells were able to replace the adherent cells in the cultures.
通过使用纯化的小鼠腹腔黏附细胞和T淋巴细胞群体,研究了促有丝分裂T淋巴细胞激活过程中的一系列事件。在用氧化剂高碘酸钠或神经氨酸酶加半乳糖氧化酶处理黏附细胞并去除促有丝分裂原后,这些细胞获得了刺激随后添加的纯化T淋巴细胞的能力。对于T淋巴细胞激活的这一过程,需要膜相互作用物质聚乙二醇、葡聚糖、无促有丝分裂活性的苹果蜗牛凝集素或灭活的仙台病毒的额外存在。经促有丝分裂原处理的腹腔黏附细胞的裂解物能够替代培养物中的黏附细胞。