Reid G K, Kargman S, Vickers P J, Mancini J A, Léveillé C, Ethier D, Miller D K, Gillard J W, Dixon R A, Evans J F
Department of Pharmacology, Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.
J Biol Chem. 1990 Nov 15;265(32):19818-23.
Previous studies involving transfection of cDNAs for 5-lipoxygenase-activating protein (FLAP) and 5-lipoxygenase into osteosarcoma cells have shown that both these proteins are essential for leukotriene synthesis (Dixon, R. A. F., Diehl, R. E., Opas, E., Rands, E., Vickers, P. J., Evans, J. F., Gillard, J. W., and Miller, D. K. (1990) Nature 343, 282-284). In the present study we show that FLAP is present in a variety of cells known to produce leukotrienes, but is absent from a number of cells which do not synthesize leukotrienes. Furthermore, differentiation of the human promyelocytic HL-60 cell line towards granulocytic cells following exposure to dimethylsulfoxide is associated with the concurrent induction of both FLAP and 5-lipoxygenase and an increased capacity to synthesize leukotrienes. Cellular leukotriene synthesis in this system is functionally dependent on FLAP as shown by its inhibition by the leukotriene biosynthesis inhibitor MK-886, a compound which specifically binds to FLAP.
先前涉及将5-脂氧合酶激活蛋白(FLAP)和5-脂氧合酶的cDNA转染到骨肉瘤细胞中的研究表明,这两种蛋白对于白三烯的合成都是必不可少的(狄克逊,R.A.F.,迪尔,R.E.,奥帕斯,E.,兰兹,E.,维克斯,P.J.,埃文斯,J.F.,吉拉德,J.W.,以及米勒,D.K.(1990年)《自然》343卷,282 - 284页)。在本研究中,我们表明FLAP存在于多种已知可产生白三烯的细胞中,但在许多不合成白三烯的细胞中不存在。此外,人早幼粒细胞HL - 60细胞系在暴露于二甲基亚砜后向粒细胞分化,这与同时诱导FLAP和5-脂氧合酶以及增加合成白三烯的能力有关。该系统中的细胞白三烯合成在功能上依赖于FLAP,白三烯生物合成抑制剂MK - 886对其的抑制作用表明了这一点,MK - 886是一种与FLAP特异性结合的化合物。