Sugane K, Kasahara T, Shioiri-Nakano K
Jpn J Exp Med. 1975 Feb;45(1):19-24.
The production of macrophage migration inhibitory factor (MIF) was studied with mouse B spleen cells and with the low density subpopulation of thymus cells (T cells) stimulated by phytomitogens. MIF was released from mouse B cells when stimulated by Sepharose-PWM but was not released by Sepharose-Con A. MIF was produced by the low density subpopulation of thymus cells stimulated by Sepharose-Con A. MIF from B cells could not be distinguished from that of the low density subpopulation of thymus cells by gel filtration on Sephadex G-100 column. The molecular size of both MIF was calculated to be 45,000-55,000 dalton.
用植物有丝分裂原刺激小鼠B脾细胞和低密度胸腺细胞亚群(T细胞),研究巨噬细胞移动抑制因子(MIF)的产生。当用琼脂糖-美洲商陆有丝分裂原(Sepharose-PWM)刺激时,MIF从小鼠B细胞中释放出来,但用琼脂糖-刀豆蛋白A(Sepharose-Con A)刺激时则不释放。MIF由琼脂糖-刀豆蛋白A刺激的低密度胸腺细胞亚群产生。通过Sephadex G-100柱上的凝胶过滤,无法区分来自B细胞的MIF和低密度胸腺细胞亚群的MIF。两种MIF的分子大小经计算为45,000-55,000道尔顿。