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人胎盘外膜上Fcγ结合位点的表达

Expression of Fc gamma binding sites on human extraplacental membranes.

作者信息

Wood G W, Johnson B, Halsey J F, King C R

出版信息

Am J Reprod Immunol (1980). 1983 Jul-Aug;4(1):21-6. doi: 10.1111/j.1600-0897.1983.tb00248.x.

Abstract

Binding sites for the Fc portion of immunoglobulin G (IgG) molecules (Fc gamma BS) were identified on amnionic epithelial cells and chorionic trophoblast cells in human extraplacental membranes using direct immunofluorescence with labeled human IgG. The binding sites are similar to FC gamma BS on placental trophoblast in their specificity and high degree of relative binding affinity for IgG monomers. Neither immunoglobulin A (IgA) nor IgM bound to a significant degree to the membranes. Binding was completely inhibited with unlabeled IgG but not F(ab')2 fragments of IgG. Studies on isolated amnion cells demonstrated that the binding sites are expressed on the cell membrane. At the level of sensitivity of the immunohistologic methods used, aggregated IgG or antigen-antibody complexes failed to bind amnionic epithelial cells or chorionic trophoblasts. This is in contrast to Fc gamma BS on macrophages which, being present in the same tissue, failed to exhibit significant binding of deaggregated IgG but bound complexes avidly.

摘要

利用标记的人免疫球蛋白G(IgG)进行直接免疫荧光法,在人胎盘外膜的羊膜上皮细胞和绒毛膜滋养层细胞上鉴定出了免疫球蛋白G(IgG)分子Fc部分的结合位点(FcγBS)。这些结合位点在特异性以及对IgG单体的相对结合亲和力高度方面,与胎盘滋养层上的FcγBS相似。免疫球蛋白A(IgA)和免疫球蛋白M(IgM)均未大量结合至这些膜上。未标记的IgG可完全抑制结合,但IgG的F(ab')2片段则不能。对分离出的羊膜细胞的研究表明,这些结合位点表达于细胞膜上。在所使用的免疫组织学方法的灵敏度水平上,聚集的IgG或抗原 - 抗体复合物未能结合羊膜上皮细胞或绒毛膜滋养层细胞。这与巨噬细胞上的FcγBS形成对比,巨噬细胞存在于同一组织中,未表现出对解聚IgG的显著结合,但能 avidly结合复合物。 (注:avidly这个词在中文里不太好找到完全对应的词,这里保留英文未翻译,建议根据上下文进一步确定其准确含义后处理)

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