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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Differential expression of thromboxane A synthase and prostaglandin H synthase in megakaryocytic cell line
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Differential expression of thromboxane A synthase and prostaglandin H synthase in megakaryocytic cell line

机译:血核烷A合酶和前列腺素H合酶在巨核细胞系中的差异表达

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We determined the expression of isoforms of prostaglandin H synthase (PGHS) and thromboxane A synthase (TXAS) in a human megakaryocyte cell line (MEG-01. The basal levels of full-length TXAS mRNA and the 60 kDa TXAS protein were high when compared to those of PGHS-1 and PGHS-2 in uninduced cells. Despite a high TXAS level, uninduced MEG-01 cells synthesized only a small amount of thromboxane A2 (TXA2) due to limited PGHS-1 or PGHS-2 expressions. Following PMA induction there was little change in TXAS. PGHS-2 mRNA was significantly increased at only 3 h of PMA treatment and the level declined rapidly, whereas PGHS-1 mRNA and protein levels were concordantly stimulated. Induction of PGHS-1 reached plateau on day 3 of PMA treatment. Analysis of arachidonate metabolism in cells induced by PMA for 3 and 5 days showed a high level of PGH2 synthesis which exceeded the TXAS capacity for TXA2 synthesis. Only traces of PGHS-2 mRNA and alternate-spliced TXAS mRNA were detected in human platelets. We conclude that TXAS and PGHS are differentially expressed in MEG-01 during PMA-induced differentiation.
机译:我们确定了人类巨核细胞系(MEG-01)中前列腺素H合酶(PGHS)和血栓烷A合酶(TXAS)的同工型的表达。全长TXAS mRNA和60 kDa TXAS蛋白的基础水平较高与未诱导细胞中PGHS-1和PGHS-2的表达相比,尽管TXAS水平很高,但由于PGHS-1或PGHS-2表达受限,未诱导的MEG-01细胞仅合成了少量的血栓烷A2(TXA2)。诱导后TXAS几乎没有变化,仅在PMA处理3小时后PGHS-2 mRNA显着增加,并且水平迅速下降,而PGHS-1 mRNA和蛋白水平受到一致刺激,第3天PGHS-1诱导达到平稳。对PMA诱导的细胞进行3天和5天的花生四烯酸代谢分析表明,PGH2的合成水平很高,超过了TXAS2合成的TXAS能力,仅检测到了PGHS-2 mRNA和交替剪接的TXAS mRNA的痕迹。人血小板。我们得出结论,在PMA诱导的分化过程中,TXAS和PGHS在MEG-01中差异表达。

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