Young B
Immunology. 1982 May;46(1):37-42.
The first paper in this series reported that it was possible to reconstitute the response of low concentrations of mouse spleen lymphocytes to concanavalin A (Con A) by adding smaller numbers of peritoneal exudate cells (PEC) to the cultures. In this paper it is shown that the role of the PEC in this system can be partially replaced by conditioned medium (CM) prepared from PEC cultures or completely replaced by CM taken from lymphocytes cultured at optimal concentration. These CM were inactive unless fresh Con A was added to the assay cultures. Activity was present in Cm which was incubated with lymphocytes or PEC for the shortest possible time but maximal activity was found after 24 hr of incubation. Activity was also found in Cm prepared in the absence of Con A. Only in the case of lymphocytes cultured at optimal concentration for 24 hr was there substantially more activity in the CM thus prepared if Con A was present. PEC preparations depleted of T lymphocytes produced as much activity in Cm as the untreated control. CM produced by PEC was less sensitive to heat treatment or to freezing and thawing than that produced by lymphocyte cultures.
本系列的第一篇论文报道,通过向培养物中添加少量腹膜渗出细胞(PEC),可以重建低浓度小鼠脾淋巴细胞对刀豆蛋白A(Con A)的反应。本文表明,该系统中PEC的作用可部分由PEC培养物制备的条件培养基(CM)替代,或完全由最佳浓度培养的淋巴细胞产生的CM替代。除非向检测培养物中添加新鲜的Con A,否则这些CM无活性。与淋巴细胞或PEC孵育最短时间的CM存在活性,但孵育24小时后活性最大。在无Con A的情况下制备的CM中也发现了活性。只有在最佳浓度培养24小时的淋巴细胞的情况下,如果存在Con A,由此制备的CM中的活性才会显著增加。去除T淋巴细胞的PEC制剂在CM中产生的活性与未处理的对照一样多。PEC产生的CM比淋巴细胞培养物产生的CM对热处理或冻融更不敏感。