Holtzman M J, Hansbrough J R, Rosen G D, Turk J
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Biochim Biophys Acta. 1988 Dec 16;963(3):401-13. doi: 10.1016/0005-2760(88)90308-6.
To determine identities of mediators and mechanisms for their release from pulmonary airway epithelial cells, we examined the capacities of epithelial cells from human, dog and sheep airways to incorporate, release and oxygenate arachidonic acid. Purified cell suspensions were incubated with radiolabeled arachidonic acid and/or ionophore A23187; fatty acid esterification and hydrolysis were traced chromatographically, and oxygenated metabolites were identified using high-pressure liquid chromatography and mass-spectrometry. In each species, cellular uptake of 10 nM arachidonic acid was concentrated in the phosphatidylcholine, phosphatidylinositol and phosphatidylethanolamine fractions, and subsequent incubation with 5 microM A23187 caused release of 10-12% of the radiolabeled pool selectively from phosphatidylcholine and phosphatidylinositol. By contrast, the products of arachidonic acid oxygenation were species-dependent and in the case of human cells were also novel: A23187-stimulated human epithelial cells converted arachidonic acid predominantly to 15-hydroxyeicosatetraenoic acid (15-HETE) and two distinct 8,15-diols in addition to prostaglandin (PG) E2 and PGF2 alpha. Cell incubation with exogenous arachidonic acid (2.0-300 microM) led to progressively larger amounts of 15-HETE and the dihydroxy, epoxyhydroxy and keto acids characteristic of arachidonate 15-lipoxygenase. Both dog and sheep cells converted exogenous or endogenous arachidonic acid to low levels of 5-lipoxygenase products, including leukotriene B4 without significant 15-lipoxygenase activity. In the cyclooxygenase series, sheep cells selectively released PGE2, while dog cells generated predominantly PGD2. The findings demonstrate that stereotyped esterification and phospholipase activities are expressed at uniform levels among airway epithelial cells from these species, but pathways for oxygenating arachidonic acid allow mediator diversity depending greatly on species and little on arachidonic acid presentation.
为了确定介质的身份及其从肺气道上皮细胞释放的机制,我们研究了来自人、狗和绵羊气道的上皮细胞摄取、释放和氧化花生四烯酸的能力。将纯化的细胞悬液与放射性标记的花生四烯酸和/或离子载体A23187一起孵育;通过色谱法追踪脂肪酸的酯化和水解过程,并使用高压液相色谱和质谱法鉴定氧化代谢产物。在每个物种中,10 nM花生四烯酸的细胞摄取集中在磷脂酰胆碱、磷脂酰肌醇和磷脂酰乙醇胺组分中,随后与5 μM A23187孵育会导致放射性标记池中有10 - 12%的花生四烯酸选择性地从磷脂酰胆碱和磷脂酰肌醇中释放出来。相比之下,花生四烯酸氧化产物具有物种依赖性,就人类细胞而言,这些产物还是新发现的:A23187刺激的人类上皮细胞将花生四烯酸主要转化为15 - 羟基二十碳四烯酸(15 - HETE)和两种不同的8,15 - 二醇,此外还有前列腺素(PG)E2和PGF2α。用外源性花生四烯酸(2.0 - 300 μM)孵育细胞会导致15 - HETE以及花生四烯酸15 - 脂氧合酶特有的二羟基、环氧羟基和酮酸的生成量逐渐增加。狗和绵羊细胞都将外源性或内源性花生四烯酸转化为低水平的5 - 脂氧合酶产物,包括白三烯B4,且没有明显的15 - 脂氧合酶活性。在环氧化酶系列中,绵羊细胞选择性释放PGE2,而狗细胞主要生成PGD2。这些发现表明,在这些物种的气道上皮细胞中,定型的酯化和磷脂酶活性以统一水平表达,但花生四烯酸的氧化途径导致介质具有多样性,这很大程度上取决于物种,而很少取决于花生四烯酸的呈现方式。