Pick E, Godny Y, Gold E F
Eur J Immunol. 1975 Aug;5(8):584-7. doi: 10.1002/eji.1830050816.
The role of immunoglobulin-bearing cells in the production of macrophage migration inhibitory factor (MIF) by tuberculin-stimulated lymphocytes of guinea pigs, immunized with complete Freund's adjuvant, was studied. It was found that: (1) pretreatment of lymphocytes with rabbit anti-guinea pig IgG (anti-IgG) does not block antigen-induced MIF production. (2) Passage of lymphocytes through double layer IgG-anti-IgG gelatin bead columns (the preparation of which is described) abolishes MIF formation by the eluted cells. Cells retained on the columns can be recovered and where shown to produce MIF, when stimulated by antigen. (3) Pulsing of lymphocytes with anti-IgG, for 2 h at 37degreesC, results in MIF synthesis by the cells cultured in medium, in the absence of specific antigen. These findings indicate that cells bearing Ig or Ig fragments are either able to secrete MIF themselves, upon stimulation with antigen or anti-IgG, or are required for MIF production by a different cell type.
研究了用完全弗氏佐剂免疫的豚鼠经结核菌素刺激的淋巴细胞产生巨噬细胞移动抑制因子(MIF)过程中,携带免疫球蛋白细胞的作用。结果发现:(1)用兔抗豚鼠IgG(抗IgG)预处理淋巴细胞并不阻断抗原诱导的MIF产生。(2)淋巴细胞通过双层IgG-抗IgG明胶珠柱(文中描述了其制备方法)后,洗脱的细胞不再形成MIF。保留在柱上的细胞可以回收,经抗原刺激后可产生MIF。(3)在37℃用抗IgG脉冲淋巴细胞2小时,可使细胞在无特异性抗原的培养基中培养时合成MIF。这些发现表明,携带Ig或Ig片段的细胞,要么在受到抗原或抗IgG刺激时自身能够分泌MIF,要么是另一种细胞类型产生MIF所必需的。