Zocchi M R, Poggi A
Istituto Scientifico San Raffaele, Milan, Italy.
Cell Immunol. 1991 Aug;136(1):105-12. doi: 10.1016/0008-8749(91)90385-o.
We have observed that the CD28 molecule was present on the cell surface of a large fraction of resting CD3- thymocytes (40 to 100%). Interestingly, the majority (greater than 90%) of surface CD3-CD28-cells reacted in the cytoplasm with anti-CD28 (CK248, 9.3) and anti-CD3 epsilon chain mAbs (Leu4, OKT3). Along this line, we found that CD28 surface expression could be induced within 18 hr on CD3-CD28- thymocytes using very low doses of phorbol-13-myristate-12-acetate (PMA). This event was accompanied by the appearance of CD25 and CD69 activation antigens but not of CD3/TCR complex. These results were further confirmed by immunoprecipitation studies. It is noteworthy that the T-cell activation pathway initiated via the CD28 molecule is functional in resting CD3- thymocytes in the presence of PMA and/or IL2. Finally, stimulation of CD3- immature thymocytes via CD28 gave rise to a large fraction (about one-third) of CD3-CD8+ cells.
我们观察到,大部分静止的CD3 - 胸腺细胞(40%至100%)的细胞表面存在CD28分子。有趣的是,大多数(超过90%)表面CD3 - CD28 - 细胞在细胞质中与抗CD28(CK248,9.3)和抗CD3 ε链单克隆抗体(Leu4,OKT3)发生反应。据此,我们发现使用极低剂量的佛波醇 - 13 - 肉豆蔻酸酯 - 12 - 乙酸酯(PMA)可在18小时内诱导CD3 - CD28 - 胸腺细胞表面表达CD28。这一事件伴随着CD25和CD69激活抗原的出现,但未出现CD3/TCR复合物。免疫沉淀研究进一步证实了这些结果。值得注意的是,在PMA和/或IL2存在的情况下,通过CD28分子启动的T细胞激活途径在静止的CD3 - 胸腺细胞中具有功能。最后,通过CD28刺激CD3 - 未成熟胸腺细胞产生了很大一部分(约三分之一)CD3 - CD8 + 细胞。