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A23187刺激的人白细胞中胞质15-脂氧合酶活性丧失:涉及易位过程?

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

作者信息

Bongrazio M, Roscher A, Ludwig P, Nigam S

机构信息

Department of Gynecology, Free University Berlin, Federal Republic of Germany.

出版信息

Eicosanoids. 1992;5(3-4):191-5.

PMID:1292528
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.

摘要

我们将研究重点放在用A23187和花生四烯酸(AA)刺激的人白细胞中15-脂氧合酶的亚细胞重新分布上。我们发现,在受刺激细胞的胞质组分中,以15-羟基二十碳四烯酸(15-HETE)衡量的15-脂氧合酶(15-LO)活性比对照低65%。然而,在细胞膜中未发现活性。这种效应在孵育2分钟内完成,并且与外源添加的AA呈剂量依赖性相关。当细胞在不同浓度的Ca++存在下受到刺激时,未观察到15-LO活性在胞质分布上的显著差异。免疫印迹分析表明,用A23187刺激后记录到的胞质15-LO活性丧失与胞质中酶含量的相应丧失相关,提示存在转运过程的可能性。然而,在我们目前的实验条件下,在细胞膜中既未发现15-LO活性,也未发现该酶。但是,添加蛋白酶抑制剂后,膜组分中的15-LO活性略有增加。尽管影响较小,但这可能表明用A23187刺激人白细胞后15-LO发生了转运。

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