Rossio J L, Ruscetti F W, Farrar W L
Lymphokine Res. 1986 Spring;5(2):163-72.
Calcium mobilization is one of the earliest quantitative biochemical events associated with extracellular messenger stimulation of cellular proliferation. Therefore, purified recombinant lymphokines Interleukin 2 (IL 2) and Interleukin 3 (IL 3) were examined for ligand stimulation of calcium mobilization with highly specific interleukin-dependent cloned cell lines. Although IL 2 and IL 3 share neither amino acid structural homologies nor cellular tissue specificity, both recombinant polypeptides induced rapid influx of calcium into quiescent cells bearing specific receptors for the ligand. Neither ligand was capable of stimulating calcium mobilization in the non-homologous target cells which differed in tissue lineage. Stimulation of calcium mobilization demonstrated characteristic threshold dose-response kinetics and was observed under conditions where intracytoplasmic calcium levels were spontaneously depleted upon ligand deprivation. These data confirm that in addition to the activation of protein kinase C, growth regulatory polypeptides of mature T lymphocytes (IL 2) and hematopoietic stem cells (IL 3) share common biochemical features of the ligand-receptor signal transduction apparatus which initiates cellular proliferation.
钙动员是与细胞外信使刺激细胞增殖相关的最早的定量生化事件之一。因此,利用高度特异性的白细胞介素依赖性克隆细胞系,检测了纯化的重组淋巴因子白细胞介素2(IL-2)和白细胞介素3(IL-3)对钙动员的配体刺激作用。尽管IL-2和IL-3既没有氨基酸结构同源性,也没有细胞组织特异性,但两种重组多肽都能诱导钙迅速流入带有该配体特异性受体的静止细胞。两种配体都不能刺激不同组织谱系的非同源靶细胞中的钙动员。钙动员的刺激表现出特征性的阈值剂量反应动力学,并且在配体剥夺后细胞质钙水平自发耗尽的条件下也能观察到。这些数据证实,除了蛋白激酶C的激活外,成熟T淋巴细胞(IL-2)和造血干细胞(IL-3)的生长调节多肽在启动细胞增殖的配体-受体信号转导装置方面具有共同的生化特征。