Sigal E, Nadel J A
Cardiovascular Research Institute, University of California, San Francisco 94143-0130.
Am Rev Respir Dis. 1988 Dec;138(6 Pt 2):S35-40. doi: 10.1164/ajrccm/138.6_Pt_2.S35.
Pulmonary epithelial cells may be primarily responsible for initiating or regulating inflammatory responses in the airways, in part by releasing chemical mediators. Among the most potent mediators of inflammation are the lipoxygenase metabolites of arachidonic acid, including the leukotrienes and the other mono- and dihydroxyeicosatetraenoic acids (HETEs). The human airway epithelium contains significant 15-lipoxygenase activity. Although some biologic functions of 15-lipoxygenase metabolites are known, further understanding of the role of this enzyme in the airway requires localization in tissue and studies of expression, regulation, and biologic activity. Towards these aims, we purified and characterized 15-lipoxygenase from eosinophil-enriched leukocytes. First, we studied cofactors that may be involved in regulating enzymatic activity. We discovered that calcium and phosphatidylcholine both enhanced, but ATP inhibited, the 15-lipoxygenase activity of highly enriched enzyme. Second, we isolated to homeogeneity, for the first time, human 15-lipoxygenase. This led to the determination of the N-terminal amino acid sequence and the discovery of homology among various mammalian lipoxygenases. Further research using purified lipoxygenase is expected to increase our understanding of the biologic roles and biochemical features of 15-lipoxygenation of arachidonic acid.
肺上皮细胞可能主要负责引发或调节气道中的炎症反应,部分原因是通过释放化学介质。花生四烯酸的脂氧合酶代谢产物是最强的炎症介质之一,包括白三烯以及其他单羟基和二羟基二十碳四烯酸(HETEs)。人呼吸道上皮含有显著的15-脂氧合酶活性。尽管已知15-脂氧合酶代谢产物的一些生物学功能,但要进一步了解该酶在气道中的作用,需要在组织中定位并研究其表达、调节和生物学活性。为了实现这些目标,我们从富含嗜酸性粒细胞的白细胞中纯化并鉴定了15-脂氧合酶。首先,我们研究了可能参与调节酶活性的辅助因子。我们发现钙和磷脂酰胆碱均增强了高度纯化酶的15-脂氧合酶活性,但ATP则抑制该活性。其次,我们首次将人15-脂氧合酶分离至同质。这使得能够确定其N端氨基酸序列,并发现各种哺乳动物脂氧合酶之间的同源性。预计使用纯化的脂氧合酶进行的进一步研究将增进我们对花生四烯酸15-脂氧合作用的生物学作用和生化特征的理解。