Ahmann G B, Nadler P I, Birnkrant A, Hodes R J
J Immunol. 1979 Aug;123(2):903-9.
The ability of subpopulations of murine spleen cells to stimulate a mixed lymphocyte response (MLR) was studied. It was found that T cells (nylon-nonadherent spleen cells) and B cells [G-10 passed and treated with rabbit anti-mouse brain serum (RAMB) and complement (C)] were poor stimulators of an MLR. In contrast, whole spleen cells or B cells plus adherent cells (RAMB +C-treated spleen cells) produced good stimulation. However, a non-T, radiation-resistant splenic adherent cell (SAC) population was up to 20 to 50 times more efficient as a stimulator of an MLR on a per cell basis than an unseparated spleen population. These SAC were shown to express Ia determinants encoded by genes in I-A and I-E/C. These results suggest that Ia+ SAC may be the predominant stimulating cells in spleen cell populations, and the preferential target for T cell recognition in cell interaction events.
对小鼠脾细胞亚群刺激混合淋巴细胞反应(MLR)的能力进行了研究。发现T细胞(尼龙非黏附性脾细胞)和B细胞[经G-10柱处理并用兔抗小鼠脑血清(RAMB)和补体(C)处理]是MLR的弱刺激剂。相比之下,全脾细胞或B细胞加黏附细胞(经RAMB +C处理的脾细胞)产生良好的刺激作用。然而,一种非T、抗辐射的脾黏附细胞(SAC)群体,以每细胞为基础作为MLR刺激剂的效率比未分离的脾细胞群体高20至50倍。这些SAC被证明表达由I-A和I-E/C基因编码的Ia决定簇。这些结果表明,Ia+ SAC可能是脾细胞群体中的主要刺激细胞,并且是细胞相互作用事件中T细胞识别的优先靶标。