Chiba K, Nishimura T, Hashimoto Y
J Immunol. 1985 Feb;134(2):1019-25.
A lymphokine inhibitory for cellular DNA synthesis (termed STIF) was isolated from the culture supernatants of concanavalin A (Con A)-stimulated SD rat spleen cells. STIF inhibited the DNA synthesis of mouse bone marrow cells as well as mouse leukemia cells. STIF has an apparent m.w. of 45,000 to 50,000 and is separable from IL 2, m.w. 20,000 to 25,000, by Sephacryl S-200 gel filtration, but not from immune interferon (IFN) having the same m.w. as STIF. Con A-Sepharose chromatography of the fraction containing STIF and IFN could separate these lymphokines into Con A-unbound and Con A-bound fractions, respectively. Further fractionation of the STIF fraction by DEAE-Sephadex A-50 or Mono Q-FPLC anion exchange chromatography indicated that the STIF fraction contained two components of STIF activity, both showing the same pI value (5.1 to 5.6) on flat-bed isoelectric focusing. STIF was characterized as a sugar-free lymphokine of trypsin-sensitive protein nature.
从伴刀豆球蛋白A(Con A)刺激的SD大鼠脾细胞培养上清液中分离出一种抑制细胞DNA合成的淋巴因子(称为STIF)。STIF抑制小鼠骨髓细胞以及小鼠白血病细胞的DNA合成。STIF的表观分子量为45,000至50,000,通过Sephacryl S - 200凝胶过滤可与分子量为20,000至25,000的白细胞介素2分离,但不能与具有与STIF相同分子量的免疫干扰素(IFN)分离。对含有STIF和IFN的组分进行Con A-Sepharose层析可分别将这些淋巴因子分离为Con A未结合组分和Con A结合组分。通过DEAE-Sephadex A - 50或Mono Q-FPLC阴离子交换层析对STIF组分进一步分级分离表明,STIF组分含有两种具有STIF活性的成分,在平板等电聚焦上均显示相同的pI值(5.1至5.6)。STIF的特征是一种无糖的、对胰蛋白酶敏感的蛋白质性质的淋巴因子。