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首页> 外文期刊>The FEBS journal >Hypoxia reduces the expression of heme oxygenase-2 in various types of human cell lines - A possible strategy for the maintenance of intracellular heme level
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Hypoxia reduces the expression of heme oxygenase-2 in various types of human cell lines - A possible strategy for the maintenance of intracellular heme level

机译:缺氧可降低各种类型人类细胞系中血红素加氧酶2的表达-维持细胞内血红素水平的一种可能策略

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Heme oxygenase consists of two structurally related isozymes, heme oxygenase-1 and and heme oxygenase-2, each of which cleaves heme to form biliverdin, iron and carbon monoxide. Expression of heme oxygenase-1 is increased or decreased depending on cellular microenvironments, whereas little is known about the regulation of heme oxygenase-2 expression. Here we show that hypoxia (1% oxygen) reduces the expression levels of heme oxygenase-2 mRNA and protein after 48 h of incubation in human cell lines, including Jurkat T-lymphocytes, YN-1 and K562 erythroleukemia, HeLa cervical cancer, and HepG2 hepatoma, as judged by northern blot and western blot analyses. In contrast, the expression level of heme oxygenase-1 mRNA varies under hypoxia, depending on the cell line; it was increased in YN-1 cells, decreased in HeLa and HepG2 cells, and remained undetectable in Jurkat and K562 cells. Moreover, heme oxygenase-1 protein was decreased in YN-1 cells under the conditions used, despite the induction of heme oxygenase-1 mRNA under hypoxia. The heme oxygenase activity was significantly decreased in YN-1, K562 and HepG2 cells after 48 h of hypoxia. To explore the mechanism for the hypoxia-mediated reduction of heme oxygenase-2 expression, we showed that hypoxia shortened the half-life of heme oxygenase-2 mRNA (from 12 h to 6 h) in YN-1 cells, without affecting the half-life of heme oxygenase-1 mRNA (9.5 h). Importantly, the heme contents were increased in YN-1, HepG2 and HeLa cells after 48 h of incubation under hypoxia. Thus, the reduced expression of heme oxygenase-2 may represent an important adaptation to hypoxia in certain cell types, which may contribute to the maintenance of the intracellular heme level.
机译:血红素加氧酶由两种结构上相关的同工酶:血红素加氧酶-1和血红素加氧酶2组成,它们各自裂解血红素形成联蛋白,铁和一氧化碳。血红素加氧酶-1的表达根据细胞的微环境增加或减少,而对血红素加氧酶2的表达的调控知之甚少。在这里,我们显示缺氧(1%氧气)在人细胞株(包括Jurkat T淋巴细胞,YN-1和K562红白血病,HeLa宫颈癌和通过Northern印迹和Western印迹分析判断为HepG2肝癌。相比之下,血红素加氧酶-1 mRNA的表达水平在缺氧条件下会有所不同,具体取决于细胞系。它在YN-1细胞中增加,在HeLa和HepG2细胞中减少,在Jurkat和K562细胞中仍未检测到。此外,尽管在低氧条件下诱导了血红素加氧酶-1 mRNA,但在使用条件下,YN-1细胞中的血红素加氧酶-1蛋白降低。缺氧48小时后,YN-1,K562和HepG2细胞的血红素加氧酶活性显着降低。为了探索缺氧介导的血红素加氧酶-2表达降低的机制,我们发现缺氧缩短了YN-1细胞中血红素加氧酶-2 mRNA的半衰期(从12 h到6 h),而没有影响一半血红素加氧酶-1 mRNA的寿命(9.5小时)。重要的是,在缺氧条件下孵育48小时后,YN-1,HepG2和HeLa细胞中的血红素含量增加。因此,血红素加氧酶-2表达的降低可能代表在某些细胞类型中对缺氧的重要适应,这可能有助于维持细胞内血红素水平。

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