Cosio F G, Hoidal J R, Douglas S D, Michael A F
J Lab Clin Med. 1982 Sep;100(3):469-76.
The Fc receptor of human monocytes and pulmonary macrophages has been evaluated quantitatively by binding of radiolabeled soluble IC. On both cell types, binding was mediated by saturable surface receptors specifically inhibited by aggregated human IgG1 and IgG3. The affinity of the Fc receptor was similar on monocytes and pulmonary macrophages from nonsmokers, but macrophages demonstrated four to 13 times more surface receptors than circulating monocytes. No difference in Fc receptor binding of monocytes was observed between cigarette smokers and nonsmokers. However, pulmonary macrophages from smokers demonstrated a significantly lower Fc receptor affinity than did those of nonsmokers, although the number of Fc receptors was the same.
通过放射性标记的可溶性免疫复合物的结合,对人单核细胞和肺巨噬细胞的Fc受体进行了定量评估。在这两种细胞类型上,结合是由可饱和的表面受体介导的,这些受体被聚集的人IgG1和IgG3特异性抑制。非吸烟者的单核细胞和肺巨噬细胞上Fc受体的亲和力相似,但巨噬细胞表面受体的数量比循环单核细胞多4至13倍。吸烟者和非吸烟者的单核细胞在Fc受体结合方面未观察到差异。然而,吸烟者的肺巨噬细胞Fc受体亲和力明显低于非吸烟者,尽管Fc受体的数量相同。