Iversen L, Svendsen M, Kragballe K
Department of Dermatology, Marselisborg Hospital, University of Aarhus, Denmark.
Acta Derm Venereol. 1996 Nov;76(6):424-8. doi: 10.2340/0001555576424428.
Leukotriene A4 hydrolase is a key enzyme in the biosynthesis of leukotriene B4, a potent pro-inflammatory compound. The purpose of this study was to determine the capacity of antiinflammatory and anti-proliferative compounds to regulate the levels and activity of leukotriene A4 hydrolase in cultured human keratinocytes. The content of leukotriene A4 hydrolase was determined by Western blot analysis, and the activity of leukotriene A4 hydrolase was expressed as the leukotriene B4 formation after incubation of keratinocyte cultures with leukotriene A4. Leukotriene B4 was measured by revered-phase high performance liquid chromatography. Preincubation for 10 min of the cultured keratinocytes with the leukotriene A4 hydrolase inhibitor RP 64699 (0.1-10 microM) caused a significant dose-dependent inhibition of leukotriene B4 formation (IC50 = 0.7 microM). Cyclosporin A (0.1 micrograms/ml and 1.0 micrograms/ml) had no direct effect on leukotriene A4 hydrolase activity, but after incubation for 72 h there was a decrease in the mean leukotriene B4 formation per culture dish (35% and 48%, respectively). The decreased leukotriene B4 formation was caused mainly by a decrease in the mean leukotriene A4 hydrolase content per mg protein (30.1% at 0.1 micrograms/ml cyclosporin A and 40.0% at 1.0 micrograms/ml cyclosporin A), although keratinocyte proliferation was also slightly decreased. Incubations with 1.25-dihydroxyvitamin D3 (10(-7)-10(-10) M), all-trans retinoic acid (10(-6)-10(-10) M), eicosartienoic acid (10(-6)-10(-8) M), dexamethasone (10(-5)-10(-7) M), interferon-gamma (10 and 100 units/ml) or methotrexate (0.1-10 micrograms/ml) had no effect on either the leukotriene B4 formation or the amount of leukotriene A4 hydrolase in keratinocyte cultures. These results show that cyclosporin A, in contrast to other anti-inflammatory and anti-proliferative compounds, inhibits the level of leukotriene A4 hydrolase in keratinocyte cultures. Since similar cyclosporin A concentrations are obtained during treatment of psoriasis with cyclosporin A, the effect on leukotriene A4 hydrolase may play a role in the anti-inflammatory action of cyclosporin A.
白三烯A4水解酶是白三烯B4生物合成中的关键酶,白三烯B4是一种强效促炎化合物。本研究的目的是确定抗炎和抗增殖化合物调节培养的人角质形成细胞中白三烯A4水解酶水平和活性的能力。通过蛋白质印迹分析测定白三烯A4水解酶的含量,白三烯A4水解酶的活性以角质形成细胞培养物与白三烯A4孵育后白三烯B4的生成量来表示。白三烯B4通过反相高效液相色谱法测定。用白三烯A4水解酶抑制剂RP 64699(0.1 - 10微摩尔)对培养的角质形成细胞预孵育10分钟,可导致白三烯B4生成量呈显著的剂量依赖性抑制(半数抑制浓度 = 0.7微摩尔)。环孢素A(0.1微克/毫升和1.0微克/毫升)对白三烯A4水解酶活性无直接影响,但孵育72小时后,每个培养皿中的平均白三烯B4生成量减少(分别为35%和48%)。白三烯B4生成量的减少主要是由于每毫克蛋白质中白三烯A4水解酶平均含量的降低(0.1微克/毫升环孢素A时降低30.1%,1.0微克/毫升环孢素A时降低40.0%),尽管角质形成细胞增殖也略有减少。用1,25 - 二羟基维生素D3(10^(-7) - 10^(-10)摩尔)、全反式维甲酸(10^(-6) - 10^(-10)摩尔)、二十碳五烯酸(10^(-6) - 10^(-8)摩尔)、地塞米松(10^(-5) - 10^(-7)摩尔)、干扰素 - γ(10和100单位/毫升)或甲氨蝶呤(0.1 - 10微克/毫升)孵育对角质形成细胞培养物中的白三烯B4生成量或白三烯A4水解酶量均无影响。这些结果表明,与其他抗炎和抗增殖化合物不同,环孢素A可抑制角质形成细胞培养物中白三烯A4水解酶的水平。由于在用环孢素A治疗银屑病期间可获得相似的环孢素A浓度,因此对白三烯A4水解酶的作用可能在环孢素A的抗炎作用中发挥作用。