Toyohira Y, Yanagihara N, Minami K, Ueno S, Uezono Y, Tachikawa E, Kondo Y, Kashimoto T, Izumi F
Department of Pharmacology, University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.
J Neurochem. 1998 Apr;70(4):1441-7. doi: 10.1046/j.1471-4159.1998.70041441.x.
The aim of this study was to investigate the effect of long-term treatment with interferon (IFN)-alpha on the noradrenaline transporter of bovine adrenal medullary cells. Treatment of cultured adrenal medullary cells with IFN-alpha caused a decrease in uptake of [3H]noradrenaline by the cells in time (4-48 h)- and concentration (300-1,000 U/ml)-dependent manners. IFN-beta also inhibited [3H]noradrenaline uptake to a lesser extent than did IFN-alpha, whereas IFN-gamma had little effect. An anti-IFN-alpha antibody reduced the effect of IFN-alpha on [3H]noradrenaline uptake. Saturation analysis of [3H]noradrenaline uptake showed that the inhibitory effect of IFN-alpha was due to a reduction in the maximal uptake velocity (Vmax) values without altering apparent Michaelis constant (Km) values. Incubation of cells with IFN-alpha caused a translocation of protein kinase C from the soluble to the particulate fraction in the cells. The effect of IFN-alpha on [3H]noradrenaline uptake was diminished in protein kinase C-down-regulated cells. Incubation of cells with IFN-alpha for 48 h significantly reduced the specific binding of [3H]desipramine to crude plasma membranes isolated from cells. Scatchard analysis of [3H]desipramine binding revealed that IFN-alpha decreased the maximal binding (Bmax) values without any change in the dissociation constant (K(D)) values. These findings suggest that IFN-alpha suppresses the function of noradrenaline transporter by reducing the density of the transporter in cell membranes through, at least in part, a protein kinase C pathway.
本研究的目的是调查长期使用α干扰素(IFN)治疗对牛肾上腺髓质细胞去甲肾上腺素转运体的影响。用α干扰素处理培养的肾上腺髓质细胞,导致细胞对[3H]去甲肾上腺素的摄取随时间(4 - 48小时)和浓度(300 - 1000 U/ml)呈依赖性降低。β干扰素对[3H]去甲肾上腺素摄取的抑制作用也小于α干扰素,而γ干扰素几乎没有作用。抗α干扰素抗体可降低α干扰素对[3H]去甲肾上腺素摄取的影响。[3H]去甲肾上腺素摄取的饱和分析表明,α干扰素的抑制作用是由于最大摄取速度(Vmax)值降低,而表观米氏常数(Km)值未改变。用α干扰素孵育细胞导致蛋白激酶C从细胞中的可溶性部分转移到颗粒部分。在蛋白激酶C下调的细胞中,α干扰素对[3H]去甲肾上腺素摄取的影响减弱。用α干扰素孵育细胞48小时可显著降低[3H]地昔帕明与从细胞中分离的粗制质膜的特异性结合。[3H]地昔帕明结合的Scatchard分析表明,α干扰素降低了最大结合(Bmax)值,而解离常数(KD)值没有任何变化。这些发现表明,α干扰素至少部分通过蛋白激酶C途径降低细胞膜上去甲肾上腺素转运体的密度,从而抑制其功能。