Kargman S, Prasit P, Evans J F
Department of Pharmacology, Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.
J Biol Chem. 1991 Dec 15;266(35):23745-52.
We have demonstrated translocation of HL-60 cell 5-lipoxygenase to a membrane compartment in response to both the calcium ionophore A23187 and the receptor-mediated stimulus, N-formyl-methionyl-leucyl-phenylalanine (fMLP). In addition, we have shown inhibition of A23187- and fMLP-induced 5-lipoxygenase translocation by an indole and a quinoline leukotriene synthesis inhibitor, MK-886 and L-674,573, respectively. Selectivity of inhibition of 5-lipoxygenase translocation in both fMLP- or A23187-challenged cells is shown using the indole L-583,916 and quinoline L-671,480, which neither inhibit leukotriene synthesis nor inhibit 5-lipoxygenase translocation. The present study in HL-60 cells is the first demonstration of the selective inhibition of 5-lipoxygenase translocation by quinoline leukotriene synthesis inhibitors, exemplified by L-674,573. Also described here is the first demonstration of 5-lipoxygenase translocation and inhibition in response to a stimulus other than A23187, namely the receptor-mediated stimulus, fMLP.
我们已经证明,HL-60细胞的5-脂氧合酶会响应钙离子载体A23187和受体介导的刺激物N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(fMLP)而转位至膜区室。此外,我们还表明,吲哚类和喹啉类白三烯合成抑制剂MK-886和L-674,573分别可抑制A23187和fMLP诱导的5-脂氧合酶转位。使用吲哚L-583,916和喹啉L-671,480可显示出在fMLP或A23187刺激的细胞中对5-脂氧合酶转位抑制的选择性,这两种物质既不抑制白三烯合成,也不抑制5-脂氧合酶转位。HL-60细胞中的本研究首次证明了喹啉类白三烯合成抑制剂(如L-674,573)对5-脂氧合酶转位的选择性抑制。这里还首次描述了5-脂氧合酶响应除A23187之外的刺激物(即受体介导的刺激物fMLP)而发生的转位和抑制。