Fox E J, Cook R G, Lewis D E, Rich R R
J Clin Invest. 1986 Jul;78(1):214-20. doi: 10.1172/JCI112554.
To define molecular signals elaborated by inducer populations supporting growth or differentiation of T8+ cells, we collected supernatants of pokeweed mitogen (PWM)-stimulated cultures depleted of T8+ cells. When added to purified T8+ cells, these supernatants caused significant proliferation. PWM plus interleukin 2 (IL-2) in amounts equivalent to those in the supernatant could not reconstitute the response caused by the supernatant. T8+ cells activated by supernatants obtained from PWM-pulsed T4+ cells suppressed fresh PWM cultures. Although exhibiting little proliferation, T8+ cells cultured for 6 d in PWM plus IL-2 still suppressed a fresh PWM response. The supernatants therefore contain an additional T suppressor cell growth factor (TsGF). Elaboration of TsGF required radiosensitive T4+Leu8+ cells. Molecular weight determination by high performance liquid chromatography gave a single peak of TsGF activity at approximately 8,000. Finally, whereas TsGF in the absence of IL-2 could not support the proliferation of T suppressor cells, it did cause T8+ cells to become strongly IL-2 receptor-positive.
为了确定由支持T8 +细胞生长或分化的诱导细胞群体产生的分子信号,我们收集了去除T8 +细胞的商陆丝裂原(PWM)刺激培养物的上清液。当将这些上清液添加到纯化的T8 +细胞中时,会引起显著的增殖。与上清液中含量相当的PWM加白细胞介素2(IL-2)无法重建上清液引起的反应。从PWM刺激过的T4 +细胞获得的上清液激活的T8 +细胞抑制新鲜的PWM培养物。尽管增殖很少,但在PWM加IL-2中培养6天的T8 +细胞仍然抑制新鲜的PWM反应。因此,上清液中含有一种额外的T抑制细胞生长因子(TsGF)。TsGF的产生需要对辐射敏感的T4 + Leu8 +细胞。通过高效液相色谱法测定分子量,在约8000处出现单一的TsGF活性峰。最后,虽然在没有IL-2的情况下TsGF不能支持T抑制细胞的增殖,但它确实使T8 +细胞强烈表达IL-2受体阳性。