Bartlett S P, Burton R C
J Immunol. 1982 Mar;128(3):1070-5.
In vitro culture of normal lymphohemopoietic cells is a complex event leading to the generation of a diverse group of effector cells. When murine spleen cells are cultured by themselves in fetal calf serum containing medium for up to 9 days, at least 3 distinct subpopulations of cytotoxic effectors can be distinguished on the basis of tumor target cell preference and expression of cell surface alloantigens. Fresh spleen cell suspensions contain 2 distinct NK cell types: NK-1.2+ NKA cells, which preferentially lyse lymphoma targets, and NK-1.2- NKB cells, which lyse nonlymphoma, mainly solid tumor targets. These NK cells account for all the cytolytic activity on day 0 of culture. NK-1.2+ NKA cells are very labile, and greater than or equal to 80% of their activity is lost within 48 hr of culture. By contrast, the activity of NKB cells increases in culture, up to 4-fold by day 6, and solid tumor target cells resistant to lysis by fresh spleen cells now become susceptible. In addition, an NK-1.2-, H-2+, Thy-1.2+, Ly-1.2+, Ly-2.2+ cytotoxic effector cell arises in culture from, or is dependent upon the presence of, NK-1.2-, Thy-1.2+ cells. This spontaneously arising "Tc" has a peak of activity between day 3 and 6 of culture, and kills a variety of lymphohemopoietic tumor cell types.
正常淋巴造血细胞的体外培养是一个复杂的过程,会导致产生多种效应细胞。当小鼠脾细胞在含胎牛血清的培养基中单独培养长达9天时,根据肿瘤靶细胞偏好和细胞表面同种异体抗原的表达,至少可以区分出3个不同的细胞毒性效应细胞亚群。新鲜脾细胞悬液包含2种不同类型的自然杀伤(NK)细胞:优先裂解淋巴瘤靶标的NK-1.2 + NKA细胞,以及裂解非淋巴瘤(主要是实体瘤靶标)的NK-1.2 - NKB细胞。这些NK细胞在培养第0天占所有细胞溶解活性。NK-1.2 + NKA细胞非常不稳定,其活性在培养48小时内损失超过或等于80%。相比之下,NKB细胞的活性在培养过程中增加,到第6天增加至4倍,并且对新鲜脾细胞裂解具有抗性的实体瘤靶细胞现在变得易感。此外,一种NK-1.2 - 、H-2 + 、Thy-1.2 + 、Ly-1.2 + 、Ly-2.2 + 细胞毒性效应细胞在培养中从NK-1.2 - 、Thy-1.2 +细胞产生或依赖于其存在而产生。这种自发产生的“Tc”在培养第3天至第6天之间具有活性峰值,并杀死多种淋巴造血肿瘤细胞类型。