Pestel J, Joseph M, Santoro F, Capron A
Ann Immunol (Paris). 1979 Jul-Aug;130C(4):507-16.
When unstimulated rat peritoneal macrophages are exposed in vitro to IC formed with BSA and specific rat anti-BSA IgG antibodies, an exocytosis of the lysosomal beta-G occurs. The maximal release of beta-G into the serum-free medium is induced, without cell lysis, by IC after a 6-h contact with the adherent cell population. This phenomenon is dose-dependent, and the percentage of beta-G in the medium is higher with IC in Ab excess than with other types of IC. In this homologous model (rat macrophages and rat antibodies) the Ag/Ab ratio of IC seems to represent an important factor of macrophage activation.
当未受刺激的大鼠腹膜巨噬细胞在体外暴露于由牛血清白蛋白(BSA)和特异性大鼠抗牛血清白蛋白IgG抗体形成的免疫复合物(IC)时,溶酶体β-葡萄糖苷酶(β-G)会发生胞吐作用。在与贴壁细胞群体接触6小时后,免疫复合物在不引起细胞裂解的情况下,可诱导β-G最大程度地释放到无血清培养基中。这种现象具有剂量依赖性,并且在抗体过量的免疫复合物作用下,培养基中β-G的百分比高于其他类型的免疫复合物。在这个同源模型(大鼠巨噬细胞和大鼠抗体)中,免疫复合物的抗原/抗体比例似乎是巨噬细胞激活的一个重要因素。