Kanagawa O, Chiller J M
J Immunol. 1985 Jan;134(1):397-403.
Functionally inducible CTL hybridomas were constructed by fusing alloantigen-specific T cells (C57BL/6 alpha-DBA/2) with cells from the rat thymoma line W/FU (C58NT)D. A cloned hybridoma line (KSH.4.13.6) that was specifically cytolytic in the presence of activated rat spleen cell supernatant fluid (rat Con A SN) lost activity when transferred to normal medium. However, a cytolytic activity could be reinduced by culturing KSH.4.13.6 cells in medium containing rat Con A SN or secondary mixed leukocyte culture SN. By using various sources of SN, it was found that cytolytic induction required two different factors. PMA-induced EL-4 SN and SN from antigen-activated cloned T cells, neither of which were capable of inducing cytolytic activity alone, were able to synergize in the cytolytic induction of KSH.4.13.6 IFN-gamma and IL 1 failed to induce cytolytic activity even in the presence of EL-4 SN. Furthermore, this hybridoma produced macrophage activating factor (MAF) upon culture in rat Con A SN, although MAF production could not be induced by either specific antigen or lectins. The kinetics of induction and loss of cytolytic activity mediated by rat Con A SN were similar to those of the induction of MAF production. However, EL-4 SN, which by itself was incapable of inducing cytolytic activity, was able to induce MAF production in the KSH.4.13.6 hybrid to an extent similar to that induced by rat Con A SN. These results suggest that the induction of cytolytic activity and of MAF production in this cloned hybridoma cell line are regulated by different mechanisms. Such a functionally inducible T cell hybrid may provide a tool for biochemical and molecular analysis of T cell function and regulation, and of the characterization of cytokines required for CTL differentiation.
通过将同种异体抗原特异性T细胞(C57BL/6α-DBA/2)与大鼠胸腺瘤系W/FU(C58NT)D的细胞融合,构建了功能可诱导的CTL杂交瘤。一个克隆的杂交瘤系(KSH.4.13.6)在活化的大鼠脾细胞上清液(大鼠伴刀豆球蛋白A上清液)存在时具有特异性细胞溶解活性,但转移到正常培养基中时活性丧失。然而,通过在含有大鼠伴刀豆球蛋白A上清液或二次混合白细胞培养上清液的培养基中培养KSH.4.13.6细胞,可以重新诱导细胞溶解活性。通过使用各种来源的上清液,发现细胞溶解诱导需要两种不同的因子。佛波酯诱导的EL-4上清液和抗原活化的克隆T细胞的上清液,单独一种都不能诱导细胞溶解活性,但它们能够在KSH.4.13.6的细胞溶解诱导中协同作用。干扰素-γ和白细胞介素1即使在EL-4上清液存在的情况下也不能诱导细胞溶解活性。此外,该杂交瘤在大鼠伴刀豆球蛋白A上清液中培养时产生巨噬细胞活化因子(MAF),尽管特异性抗原或凝集素都不能诱导MAF的产生。大鼠伴刀豆球蛋白A上清液介导的细胞溶解活性的诱导和丧失动力学与MAF产生的诱导动力学相似。然而,本身不能诱导细胞溶解活性的EL-4上清液能够在KSH.4.13.6杂交瘤中诱导MAF的产生,其程度与大鼠伴刀豆球蛋白A上清液诱导的程度相似。这些结果表明,该克隆杂交瘤细胞系中细胞溶解活性和MAF产生的诱导受不同机制调控。这种功能可诱导的T细胞杂交瘤可能为T细胞功能和调控的生化及分子分析以及CTL分化所需细胞因子的表征提供一种工具。