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首页> 外文期刊>The Korean Journal of Parasitology >Possible Role of Heme Oxygenase-1 and Prostaglandins in the Pathogenesis of Cerebral Malaria: Heme Oxygenase-1 Induction by Prostaglandin D-2 and Metabolite by a Human Astrocyte Cell Line
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Possible Role of Heme Oxygenase-1 and Prostaglandins in the Pathogenesis of Cerebral Malaria: Heme Oxygenase-1 Induction by Prostaglandin D-2 and Metabolite by a Human Astrocyte Cell Line

机译:血红素加氧酶-1和前列腺素在脑疟疾发病中的可能作用:前列腺素D-2诱导的血红素加氧酶-1和人类星形胶质细胞细胞系代谢产物

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摘要

Astrocytes are the most abundant cells in the central nervous system that play roles in maintaining the blood-brain-barrier and in neural injury, including cerebral malaria, a severe complication of Plasmodium falciparum infection. Prostaglandin (PG) D-2 is abundantly produced in the brain and regulates the sleep response. Moreover, PGD(2) is a potential factor derived from P. falciparum within erythrocytes. Heme oxygenase-1 (HO-1) is catalyzing enzyme in heme breakdown process to release iron, carbon monoxide, and biliverdin/bilirubin, and may influence iron supply to the P. falciparum parasites. Here, we showed that treatment of a human astrocyte cell line, CCF-STTG1, with PGD(2) significantly increased the expression levels of HO-1 mRNA by RT-PCR. Western blot analysis showed that PGD(2) treatment increased the level of HO-1 protein, in a dose- and time-dependent manner. Thus, PGD2 may be involved in the pathogenesis of cerebral malaria by inducing HO-1 expression in malaria patients.
机译:星形胶质细胞是中枢神经系统中最丰富的细胞,在维持血脑屏障和神经损伤(包括脑疟疾,恶性疟原虫感染的严重并发症)中发挥作用。前列腺素(PG)D-2在大脑中大量产生,并调节睡眠反应。此外,PGD(2)是源自红细胞内恶性疟原虫的潜在因子。血红素加氧酶-1(HO-1)在血红素分解过程中催化酶释放铁,一氧化碳和胆绿素/胆红素,并可能影响恶性疟原虫寄生虫的铁供应。在这里,我们显示用PGD(2)处理人星形胶质细胞系CCF-STTG1可以显着提高RT-PCR的HO-1 mRNA表达水平。蛋白质印迹分析表明,PGD(2)处理以剂量和时间依赖性方式增加了HO-1蛋白的水平。因此,PGD 2可能通过在疟疾患者中诱导HO-1表达来参与脑疟疾的发病机制。

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