Koshihara Y, Mizumura M, Murota S
J Biol Chem. 1982 Jul 10;257(13):7302-5.
Cloned mastocytoma P-815, 2-E-6 cells were used to investigate regulation of 5-lipoxygenase activity. 2-E-6 cells had high 5-lipoxygenase activity with slight 12-lipoxygenase activity. The 5-lipoxygenase activity was increased over 5-fold by treatment of the cells with 1 mM n-butyrate for 18 h. the most effective dose range being 0.1-5.0 mM. Treatment with n-butyrate for 18 h was more effective than treatment for 40 h. Addition of n-butyrate to an untreated cell homogenate had no stimulatory effect. The enhancement of 5-lipoxygenase activity by n-butyrate was accompanied by new synthesis of protein(s). 12-Lipoxygenase activity was not increased so much as 5-lipoxygenase activity by the treatment. This is the first report of stimulation of 5-lipoxygenase activity in cultured cells. The different responses of the two lipoxygenases to n-butyrate treatment strongly suggest that 5-lipoxygenase is a different enzyme from 12-lipoxygenase.
克隆的肥大细胞瘤P-815的2-E-6细胞被用于研究5-脂氧合酶活性的调节。2-E-6细胞具有较高的5-脂氧合酶活性和轻微的12-脂氧合酶活性。用1 mM正丁酸处理细胞18小时后,5-脂氧合酶活性增加了5倍以上,最有效的剂量范围是0.1-5.0 mM。用正丁酸处理18小时比处理40小时更有效。向未处理的细胞匀浆中添加正丁酸没有刺激作用。正丁酸对5-脂氧合酶活性的增强伴随着蛋白质的新合成。处理后,12-脂氧合酶活性的增加不如5-脂氧合酶活性那么多。这是关于培养细胞中5-脂氧合酶活性受刺激的首次报道。两种脂氧合酶对正丁酸处理的不同反应强烈表明5-脂氧合酶与12-脂氧合酶是不同的酶。