Beller D I, Unanue E R
J Immunol. 1981 Jan;126(1):263-9.
We have evaluated the biosynthesis and surface expression of I-A antigens by peritoneal macrophages and found that both events terminated during the 1st day in culture, in contrast to the undiminished synthesis and expression of H-2K antigens. This pattern was observed regardless of the means by which the macrophages were elicited, but was subject to modulation for a limited period of time in vitro: phagocytic stimuli were able to augment both I-A synthesis and expression. The loss of I-A and the re-expression after phagocytosis were both reflected in the stimulatory capacity of these macrophages in the mixed leukocyte reaction. Moreover, we found that I-A-bearing macrophages were lost from the exudate in vivo after irradiation. Our data suggest that, as in vitro, this phenomenon is due to the transition of individual macrophages from I-A-positive to I-A-negative, and that constant renewal is required to maintain the I-A-bearing subset in vivo.
我们评估了腹腔巨噬细胞对I-A抗原的生物合成及表面表达情况,发现这两个过程在培养的第1天就终止了,这与H-2K抗原持续合成和表达的情况形成对比。无论巨噬细胞是通过何种方式诱导产生的,均观察到这种模式,但在体外有限的时间段内它可受到调控:吞噬刺激能够增强I-A的合成和表达。I-A的丧失以及吞噬后I-A的重新表达均反映在这些巨噬细胞在混合淋巴细胞反应中的刺激能力上。此外,我们发现受照射后,体内渗出液中带有I-A的巨噬细胞会消失。我们的数据表明,与体外情况一样,这种现象是由于单个巨噬细胞从I-A阳性转变为I-A阴性所致,并且在体内需要持续更新以维持带有I-A的亚群。