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Modulation of human peripheral blood lymphocyte Fc gamma receptors by immune complexes: recovery of Fc gamma receptors in the presence of normal human serum.

机译:通过免疫复合物调节人外周血淋巴细胞Fcγ受体:在正常人血清存在下恢复Fcγ受体。

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摘要

When normal human peripheral blood lymphocytes (PBL) were incubated at 37 degrees with soluble transferrin anti-transferrin (TAT) complexes a significant reduction in the proportion of PBL bearing receptors for the reacted Fc portion of IgG(Fc gamma R) was found. Following incubation of such complex-treated PBL in normal human serum the proportion of Fc gamma R + PBL, as assessed by rosette formation with chicken erythrocytes (E) presensitized with rabbit antibody (A) was found to be significantly increased. Such serum-mediated recovery of Fc gamma R was not affected by pretreating PBL with cycloheximide. Recovery was found to be species restricted, Ca++ dependent and confined to a serum fraction containing molecules of relatively low molecular weight (less than 90,000 Mr). Following absorption with EA the restorative capacity of human serum was lost. These findings suggest that following modulation of human PBL-Fc gamma R by immune complexes, receptors may be restored to the cell surface from a serum pool of 'fluid-phase' Fc gamma R. The origin and biological significance of serum Fc gamma R is not known but it is conceivable that they play an important role in immunoregulation.
机译:当正常人外周血淋巴细胞(PBL)与可溶性运铁蛋白抗运铁蛋白(TAT)复合物在37度下孵育时,发现反应的IgG Fc部分(Fc gamma R)的PBL受体的比例显着降低。在将这种经复合物处理的PBL在正常人血清中孵育后,发现FcγR + PBL的比例显着增加,该比例通过与用兔抗体(A)预先敏化的鸡红细胞(E)形成玫瑰花结评估。 FcγR的这种血清介导的恢复不受用环己酰亚胺预处理PBL的影响。发现回收是受物种限制的,Ca ++依赖性的并且被限制在包含相对低分子量的分子(小于90,000 Mr)的血清级分中。用EA吸收后,人血清的恢复能力丧失。这些发现表明,在免疫复合物调节人PBL-FcγR后,受体可能从“流体相” FcγR的血清池中恢复到细胞表面。血清FcγR的起源和生物学意义是未知,但可以想象它们在免疫调节中起重要作用。

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