Rabinovitch M, Manejias R E, Nussenzweig V
J Exp Med. 1975 Oct 1;142(4):827-38. doi: 10.1084/jem.142.4.827.
The phagocytic recognition by peritoneal macrophages plated on glass- or plastic-bound immune complexes of bovine plasma albumin (BSA) and anti-BSA was examined. Ingestion but not the attachment of erythrocytes opsonized with an IgG rich antiserum (EA) was markedly inhibited. In contrast, macrophage interactions with complement-coated (EAC) red cells, or ingestion of latex particles, yeast cell walls or glutaraldehyde-treated erythrocytes was not inhibited. Complexes prepared with pepsin-treated anti-BSA IgG were ineffective indicating a requirement for the Fc region. Inhibition of ingestion of EA was not a consequence of macrophage spreading and did not appear to be mediated by solubilized complexes or by cell-derived inhibitors of phagocytosis. Significant restoration of the ability to ingest EA was obtained when macrophages on complex-coated substrates were incubated for 4-8 h in medium enriched with mouse or fetal bovine serum. Restoration was also attained by removing macrophages from complex-coated dishes and replating onto uncoated dishes. The selective inhibition of ingestion of EA may be due to blocking of Fc receptors by the complexes but depletion of receptors by endocytosis of complexes cannot be ruled out. Alternatively, the complexes may have induced selective failure of the interiorization mechanism.
对铺在玻璃或塑料结合的牛血清白蛋白(BSA)和抗BSA免疫复合物上的腹膜巨噬细胞的吞噬识别进行了检测。用富含IgG的抗血清(EA)调理的红细胞的摄取受到显著抑制,但附着不受影响。相比之下,巨噬细胞与补体包被的(EAC)红细胞的相互作用,或乳胶颗粒、酵母细胞壁或戊二醛处理的红细胞的摄取均未受到抑制。用胃蛋白酶处理的抗BSA IgG制备的复合物无效,表明需要Fc区域。EA摄取的抑制不是巨噬细胞铺展的结果,似乎也不是由溶解的复合物或细胞源性吞噬抑制剂介导的。当复合物包被底物上的巨噬细胞在富含小鼠或胎牛血清的培养基中孵育4 - 8小时时,摄取EA的能力得到显著恢复。通过将巨噬细胞从复合物包被的培养皿中移出并重新铺在未包被的培养皿上也能实现恢复。EA摄取的选择性抑制可能是由于复合物阻断了Fc受体,但不能排除复合物通过内吞作用使受体耗竭的可能性。或者,复合物可能诱导了内化机制的选择性失效。