Loss of cytosolic 15-lipoxygenase activity in A23187-stimulated human leukocytes: involvement of a translocation process?

Eicosanoids Pub Date : 1992-01-01
M Bongrazio, A Roscher, P Ludwig, S Nigam
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Abstract

We focused our study on the subcellular redistribution of 15-lipoxygenase in human leukocytes challenged with A23187 and arachidonic acid (AA). We found that in cytosolic fractions of stimulated cells the 15-lipoxygenase (15-LO) activity, measured as 15-HETE, was 65% less than in controls. However, no activity was found in cell membranes. This effect was complete within 2 min of incubation and was correlated in a dose dependent manner to exogenously added AA. No significant difference in cytosolic distribution of 15-LO activity was observed when cells were stimulated in presence of various concentrations of Ca++. Immunoblot analysis showed that the loss of cytosolic 15-LO activity registered after challenging with A23187 was associated with a concomitant loss of the enzyme content in the cytosol, suggesting the possibility of a translocation process. Neither the 15-LO activity nor the enzyme was, however, found in the cell membrane under our present experimental conditions. But, addition of protease inhibitors showed a slight increase of 15-LO activity in the membrane fraction. Despite the small effect, this may indicate a translocation of 15-LO following challenge of human leukocytes with A23187.

在a23187刺激的人白细胞中,胞质15-脂氧合酶活性的丧失:参与了一个易位过程?
我们主要研究了A23187和花生四烯酸(AA)对人白细胞15-脂氧合酶亚细胞重分布的影响。我们发现,在受刺激细胞的细胞质组分中,15-脂氧合酶(15-LO)活性(以15-HETE测量)比对照组低65%。然而,在细胞膜中没有发现活性。这种效应在孵育2分钟内完成,并与外源添加的AA呈剂量依赖关系。在不同浓度的Ca++刺激下,细胞内15-LO活性的分布无显著差异。免疫印迹分析显示,在A23187攻击后,细胞质15-LO活性的丧失与细胞质中酶含量的丧失相关,这表明可能存在易位过程。然而,在我们目前的实验条件下,在细胞膜中没有发现15-LO活性和酶。但添加蛋白酶抑制剂后,膜组分中15-LO活性略有增加。尽管影响很小,但这可能表明在A23187攻击人白细胞后15-LO易位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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