诱导非免疫小鼠巨噬细胞发挥抗弓形虫活性的可溶性t细胞衍生因子的特性

K.K. Sethi , H. Brandis
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引用次数: 11

摘要

特异性刺激的弓形虫免疫t细胞培养的无细胞上清含有一种或多种因子,可以在体外刺激非免疫巯基乙酸盐刺激的小鼠腹腔巨噬细胞(MPM)发挥抗弓形虫活性(抗弓形虫武装因子(anti-toxoplasma arms factor, s) = ATAF)。虽然含有巨噬细胞迁移抑制因子(MIF),但在刀豆蛋白A刺激脾脏淋巴细胞培养或特异性刺激李斯特菌免疫t细胞培养的上清中未发现ATAF。结果发现,弓形虫免疫t细胞与特异性抗原一起孵育16小时,而与特异性抗原一起孵育1或6小时的t细胞产生含ATAF的上清液。此外,t细胞上清液中ATAF的产生是一个活跃的温度依赖过程,因为它需要葡萄糖来产生,并且在37°C而不是4°C的培养中出现。在放线菌素D、艾美汀或嘌呤霉素存在的情况下,用特异性抗原培养弓形虫免疫t细胞上清液中不出现ATAF,秋水仙碱对其产生无影响。研究发现,ATAF活性不受遗传限制,因为它可以诱导与提供免疫t细胞获得ATAF的菌株遗传无关的小鼠毒株的MPM抗弓形虫活性。正常MPM可吸收ATAF,胰蛋白酶化MPM不能吸收ATAF。正常淋巴细胞和胰蛋白酶化淋巴细胞均不能从活性上清液中吸收ATAF。酶处理表明,ATAF对DNase和RNase具有抗性,但暴露于胰蛋白酶或在58°C加热30分钟即可灭活。显然,粗上清中的ATAF可以在-70°C下保存4个月而不失去活性。使用«Diaflo»膜进行的实验表明,原油上清液中ATAF的分子大小在50,000-100,000之间。上述发现扩展了我们之前的观察结果,并进一步定义了ATAF的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of Soluble T-Cell Derived Factor(s) which Can Induce Non-immune Murine Macrophages to Exert Anti-toxoplasma Activity

Cell-free supernatants from cultures of specifically stimulated toxoplasmaimmune T-cells contain factor (or factors) that can in vitro arm non-immune thioglycollate stimulated mouse peritoneal macrophages (MPM) to exert antitoxoplasma activity (anti-toxoplasma arming factor(s) = ATAF). ATAF was not demonstrated in supernatants from cultures of concanavalin A stimulated spleen lymphocyte cultures or specifically stimulated listeria-immune T-cell cultures, although they contained macrophage migration inhibitory factor (MIF). It was found that toxoplama-immune T-cells incubated together with specific antigen for 16 hrs, but not those incubated for 1 or 6 hrs, yield ATAF containing supernatants. Furthermore, production of ATAF in T-cell supernatants was an active temperature dependent process, since it required glucose for its production and appeared in cultures incubated at 37 °C but not at 4°C. ATAF failed to appear in supernatants of toxoplasma-immune T-cells when cultured with specific antigen in presence of actinomycin D, emetine or puromycin but colchicine had no effect on its production. ATAF activity was found to show no genetic restrictions, in that it could induce anti-toxoplasma activity in MPM from mouse strains genetically unrelated to the strain which donated immune T-cells for obtaining ATAF. ATAF could be absorbed out with normal, but not with trypsinized MPM. Neither normal nor trypsinized lymphocytes could absorb out ATAF from active supernatants. Enzyme treatments revealed that ATAF was resistant to DNase and RNase but was inactivated by exposure to trypsin or heating at 58 °C for 30 min. Apparently, ATAF in crude supernatants could be stored at -70 °C for 4 months without loss of its activity. Experiments using «Diaflo» membranes suggest that molecular size of ATAF in crude supernatants lies in the range 50,000–100,000. The above findings have extended our previous observations and further defined the characteristics of ATAF.

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