Yaegashi Y, Nielsen P, Sing A, Galanos C, Freudenberg M A
Max-Planck-Institut für Immunbiologie, Freiburg, Germany.
J Exp Med. 1995 Mar 1;181(3):953-60. doi: 10.1084/jem.181.3.953.
The interferon (IFN) gamma production of splenocytes from closely related C57BL/10ScSn (Sn) and C57BL/10ScCr (Cr) mice was compared. Concanavalin A and CD3 monoclonal antibodies induced high levels of IFN-gamma in both Sn and Cr splenocytes. By contrast, treatment with gram-negative bacteria induced IFN-gamma only in Sn splenocytes; in Cr splenocytes, the IFN-gamma response was heavily impaired. The IFN-gamma induction by bacteria requires the cooperation of IFN-gamma-producing cells with macrophages. Depletion of macrophages from Sn splenocytes resulted in the loss of ability to produce IFN-gamma after bacterial stimulation. Reconstitution with new Sn macrophages restored the IFN-gamma responsiveness, whereas reconstitution with Cr macrophages failed to do so. Normal function of IFN-gamma-producing cells and a defective function of macrophages of Cr mice was demonstrated by evidence showing that whole or macrophage-depleted Cr splenocytes, when supplemented with Sn macrophages, acquire the ability to produce IFN-gamma in response to bacteria. A similar effect was achieved by supplementing Cr splenocytes with supernatants of bacteria-stimulated Sn macrophages or with recombinant murine IFN-beta or IFN-alpha. Preincubation of active macrophage supernatants with antibodies to IFN-beta suppressed the helper activity for Cr splenocytes. Moreover, the bacteria-induced production of IFN-gamma by Sn splenocytes could be inhibited by antibodies to murine IFN-beta. The results provide evidence that IFN-beta is an important cofactor of IFN-gamma induction, which is not induced in Cr mice by gram-negative bacteria.
比较了亲缘关系较近的C57BL/10ScSn(Sn)和C57BL/10ScCr(Cr)小鼠脾细胞中干扰素(IFN)γ的产生情况。伴刀豆球蛋白A和CD3单克隆抗体在Sn和Cr脾细胞中均诱导产生高水平的IFN-γ。相比之下,用革兰氏阴性菌处理仅在Sn脾细胞中诱导IFN-γ产生;在Cr脾细胞中,IFN-γ反应严重受损。细菌诱导的IFN-γ产生需要产生IFN-γ的细胞与巨噬细胞协同作用。从Sn脾细胞中清除巨噬细胞导致细菌刺激后产生IFN-γ的能力丧失。用新的Sn巨噬细胞重建可恢复IFN-γ反应性,而用Cr巨噬细胞重建则未能恢复。通过证据表明,当补充Sn巨噬细胞时,完整的或去除巨噬细胞的Cr脾细胞获得了对细菌产生IFN-γ的能力,从而证明了Cr小鼠产生IFN-γ的细胞功能正常而巨噬细胞功能缺陷。用细菌刺激的Sn巨噬细胞的上清液或重组鼠IFN-β或IFN-α补充Cr脾细胞也可获得类似效果。用抗IFN-β抗体预孵育活性巨噬细胞上清液可抑制对Cr脾细胞的辅助活性。此外,抗鼠IFN-β抗体可抑制Sn脾细胞由细菌诱导的IFN-γ产生。结果提供了证据表明IFN-β是IFN-γ诱导的重要辅助因子,革兰氏阴性菌在Cr小鼠中不会诱导IFN-γ产生。