Yui S, Yang D, Mikami M, Yamazaki M
Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Microbiol Immunol. 1993;37(12):961-9. doi: 10.1111/j.1348-0421.1993.tb01730.x.
We characterized the nature and reaction mode of the cell growth-inhibitory factor (here designated CGIF) from rat peritoneal exudate cells (PEC). The soluble fraction separated from the lysate of Enterococcus faecalis-induced 24 hr PEC completely inhibited Con A-induced thymocyte mitogenesis. Gel filtration chromatography showed that CGIF has a molecular weight of approximately 23-25 kDa. Isoelectric focusing with Rotofor indicates that the factor has an isoelectronic point of 5.8-6.4. CGIF was inactivated by treatment at 70 C, for 30 min or by tryptic digestion, but the activity was not destroyed by the reduction with dithiothreitol. As well as thymocyte proliferation, CGIF completely suppressed 3H-thymidine incorporation of splenocytes which were stimulated by either Con A or LPS, suggesting the factor is effective on both T and B cells. The acting point of the inhibitor appeared to be a later stage of the lymphocyte activation sequence, since it was still effective when added 28.5 hr after the addition of Con A. CGIF also reduced the viability of these cells when added with mitogens such as Con A or LPS. CGIF thus appears to be distinct from interleukin-1 receptor antagonist or transforming growth factor-beta.
我们对来自大鼠腹腔渗出细胞(PEC)的细胞生长抑制因子(此处命名为CGIF)的性质和反应模式进行了表征。从粪肠球菌诱导的24小时PEC裂解物中分离出的可溶性部分完全抑制了伴刀豆球蛋白A诱导的胸腺细胞有丝分裂。凝胶过滤色谱显示CGIF的分子量约为23 - 25 kDa。使用Rotofor进行等电聚焦表明该因子的等电点为5.8 - 6.4。CGIF在70℃处理30分钟或经胰蛋白酶消化后失活,但用二硫苏糖醇还原不会破坏其活性。除了抑制胸腺细胞增殖外,CGIF还完全抑制了由伴刀豆球蛋白A或脂多糖刺激的脾细胞的3H - 胸腺嘧啶核苷掺入,表明该因子对T细胞和B细胞均有效。抑制剂的作用点似乎是淋巴细胞激活序列的后期,因为在加入伴刀豆球蛋白A 28.5小时后添加它仍然有效。当与伴刀豆球蛋白A或脂多糖等有丝分裂原一起添加时,CGIF也会降低这些细胞的活力。因此,CGIF似乎不同于白细胞介素 - 1受体拮抗剂或转化生长因子 - β。