Kikutani H, Suemura M, Owaki H, Nakamura H, Sato R, Yamasaki K, Barsumian E L, Hardy R R, Kishimoto T
J Exp Med. 1986 Nov 1;164(5):1455-69. doi: 10.1084/jem.164.5.1455.
The expression of Fc epsilon R on human lymphocytes was studied with the anti-Fc epsilon R mAbs. Fc epsilon R was expressed on most mu+,delta+ circulating B cells, whereas T cells did not express Fc epsilon R even in patients with hyper-IgE syndrome. B cells with gamma, alpha, or epsilon phenotype did not express Fc epsilon R, moreover its expression could not be induced, suggesting that the Fc epsilon R expression was correlated with isotype switching. mu+delta+ B cells in bone marrow did not express Fc epsilon R, but PHA-sup (supernatant from PHA-stimulated cell cultures) could induce its expression, and the addition of IgE augmented this induction. Recombinant IL-2, IL-1, IFN-gamma or -beta, or purified B cell differentiation factor (BSF-2 B cell-stimulatory factor 2) could not induce Fc epsilon R expression in bone marrow B cells. IFN-gamma inhibited the Fc epsilon R expression induced by PHA-sup, suggesting that the human counterpart of BSF-1 may be responsible for Fc epsilon R expression in bone marrow B cells. B cells from patients with common variable immunodeficiency and ataxia telangiectasia did not express Fc epsilon R, but PHA-sup could induce its expression, indicating that circulating B cells of these patients are at a differentiation stage similar to B cells in bone marrow. The study showed that Fc epsilon R is a B cell-specific differentiation marker, the expression of which is restricted to a defined stage of B cell differentiation.
应用抗FcεR单克隆抗体研究了人淋巴细胞上FcεR的表达。FcεR在大多数μ⁺、δ⁺循环B细胞上表达,而T细胞即使在高IgE综合征患者中也不表达FcεR。具有γ、α或ε表型的B细胞不表达FcεR,而且其表达不能被诱导,这表明FcεR的表达与同种型转换相关。骨髓中的μ⁺δ⁺B细胞不表达FcεR,但PHA上清液(PHA刺激的细胞培养物的上清液)可诱导其表达,添加IgE可增强这种诱导作用。重组IL-2、IL-1、IFN-γ或-β,或纯化的B细胞分化因子(BSF-2 B细胞刺激因子2)不能诱导骨髓B细胞表达FcεR。IFN-γ抑制PHA上清液诱导的FcεR表达,提示BSF-1的人对应物可能负责骨髓B细胞中FcεR的表达。常见可变免疫缺陷和共济失调毛细血管扩张症患者的B细胞不表达FcεR,但PHA上清液可诱导其表达,这表明这些患者的循环B细胞处于与骨髓B细胞相似的分化阶段。该研究表明,FcεR是一种B细胞特异性分化标志物,其表达限于B细胞分化的特定阶段。