Pueringer R J, Bahns C C, Monick M M, Hunninghake G W
Department of Internal Medicine, Department of Veterans Affairs Medical Center, Iowa City, Iowa 52242.
Am J Physiol. 1992 Apr;262(4 Pt 1):L454-8. doi: 10.1152/ajplung.1992.262.4.L454.
Human alveolar macrophages stimulated with the calcium ionophore A23187 selectively release large amounts of leukotriene B4 (LTB4) and (+/-)-5-hydroxy-(6E, 8Z-11Z, 14Z)-eicosatetraenoic acid. To determine whether LTB4 release by human alveolar macrophages following A23187 stimulation required the de novo production of 5-lipoxygenase, alveolar macrophages were stimulated under conditions that would preclude a role for new enzyme production. We found that A23187-stimulated alveolar macrophages release LTB4 within 10 min following stimulation, that LTB4 release is not inhibited by protein synthesis inhibitors, and that release of LTB4 does not correlate with the de novo synthesis of the first committed enzyme, 5-lipoxygenase. In contrast, LTB4 release correlated with the translocation of 5-lipoxygenase from the cytosol to the membrane fraction of the cells following A23187 stimulation and was inhibited by MK-886. These findings show that A23187 stimulation of alveolar macrophages results in translocation of a preexistent 5-lipoxygenase from the cytosol to the membrane fraction of the cell and that this translocation of 5-lipoxygenase is associated with release of LTB4 from the cells.
用钙离子载体A23187刺激人肺泡巨噬细胞,可选择性地大量释放白三烯B4(LTB4)和(±)-5-羟基-(6E,8Z-11Z,14Z)-二十碳四烯酸。为了确定A23187刺激后人肺泡巨噬细胞释放LTB4是否需要重新产生5-脂氧合酶,在排除新酶产生作用的条件下刺激肺泡巨噬细胞。我们发现,A23187刺激的肺泡巨噬细胞在刺激后10分钟内释放LTB4,LTB4的释放不受蛋白质合成抑制剂的抑制,且LTB4的释放与第一个关键酶5-脂氧合酶的从头合成无关。相反,LTB4的释放与A23187刺激后5-脂氧合酶从细胞溶质转运到细胞膜部分相关,并被MK-886抑制。这些发现表明,A23187刺激肺泡巨噬细胞导致预先存在的5-脂氧合酶从细胞溶质转运到细胞膜部分,且这种5-脂氧合酶的转运与LTB4从细胞中释放相关。