Fujiwara H, Toossi Z, Ohnishi K, Edmonds K, Ellner J J
J Immunol. 1987 Jan 1;138(1):197-203.
U937, a human macrophage-like cell line, spontaneously produces a factor which inhibited blastogenic responses of human blood T lymphocytes stimulated with tuberculin-purified protein derivative (PPD) or phytohemagglutinin (PHA). We investigated the mechanism of suppressor action of the U937 factor. The U937 suppressor factor inhibited interleukin 2 (IL 2) production by human blood T lymphocytes stimulated with PPD or PHA. IL 1 did not overcome the inhibitory action of the U937 factor on PPD-induced IL 2 production by human blood T lymphocytes. The U937 factor also inhibited the production of IL 2 by a human leukemic cell line, JURKAT, stimulated with PHA. The U937 suppressor factor interfered with the expression of Tac antigen (IL 2 receptor) on PPD- or PHA-stimulated blood T lymphocytes. The inhibitory activity of the U937 factor on Tac expression was not affected by the addition of IL 2 or a crude lymphokine-containing T cell supernatant. Tac expression was more sensitive than IL 2 production to inhibition by U937-conditioned medium. The U937 suppressor factor was precipitable by 33 to 67% saturated ammonium sulfate and was inactivated at pH 2 or pH 11. Sephacryl S-200 Gel filtration analysis of U937 culture supernatants revealed that the inhibitory activities for blastogenesis, IL 2 production, and Tac expression co-purified in fractions with an apparent m.w. between 67,000 and 130,000. These data indicate that U937 spontaneously produces a macromolecular suppressive factor with major locus of action on the production of IL 2 and the expression of the IL 2 receptor.
U937是一种人巨噬细胞样细胞系,可自发产生一种因子,该因子能抑制经结核菌素纯化蛋白衍生物(PPD)或植物血凝素(PHA)刺激的人血T淋巴细胞的增殖反应。我们研究了U937因子的抑制作用机制。U937抑制因子可抑制经PPD或PHA刺激的人血T淋巴细胞产生白细胞介素2(IL - 2)。IL - 1不能克服U937因子对人血T淋巴细胞PPD诱导的IL - 2产生的抑制作用。U937因子也能抑制经PHA刺激的人白血病细胞系JURKAT产生IL - 2。U937抑制因子干扰了经PPD或PHA刺激的血T淋巴细胞上Tac抗原(IL - 2受体)的表达。添加IL - 2或含粗制淋巴因子的T细胞上清液不会影响U937因子对Tac表达的抑制活性。Tac表达比IL - 2产生对U937条件培养基的抑制更敏感。U937抑制因子可被33%至67%饱和度的硫酸铵沉淀,并在pH 2或pH 11时失活。对U937培养上清液进行Sephacryl S - 200凝胶过滤分析表明,对增殖、IL - 2产生和Tac表达的抑制活性在表观分子量介于67,000至130,000之间的组分中共同纯化。这些数据表明,U937自发产生一种大分子抑制因子,其主要作用位点是IL - 2的产生和IL - 2受体的表达。