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缺氧对血管内皮细胞中血红素加氧酶-1的抑制作用。

Repression of heme oxygenase-1 by hypoxia in vascular endothelial cells.

作者信息

Nakayama M, Takahashi K, Kitamuro T, Yasumoto K, Katayose D, Shirato K, Fujii-Kuriyama Y, Shibahara S

机构信息

Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, Miyagi, Japan.

出版信息

Biochem Biophys Res Commun. 2000 May 19;271(3):665-71. doi: 10.1006/bbrc.2000.2683.

Abstract

Heme oxygenase 1 (HO-1), a rate-limiting enzyme in heme catabolism, has been reported to be induced by hypoxia. Unexpectedly, here we show that expression of HO-1 mRNA is repressed by hypoxia in primary cultures of human umbilical vein endothelial cells (HUVECs), but is increased by cobalt chloride (CoCl(2)) that is known to mimic hypoxia. Under the culture conditions used, the DNA-binding and transactivation activities of hypoxia-inducible factor 1 were increased in HUVECs by hypoxia or CoCl(2). Therefore, hypoxia and cobalt showed opposing effects on HO-1 mRNA expression, despite activation of hypoxia-inducible factor 1. The half-life of HO-1 mRNA was not changed by hypoxia, but was significantly prolonged by CoCl(2). Hypoxia also represses HO-1 mRNA expression in human coronary artery endothelial cells and astrocytes. The repression of HO-1 expression may represent the adaptation to hypoxia in certain cell types.

摘要

血红素加氧酶1(HO-1)是血红素分解代谢中的一种限速酶,据报道可被缺氧诱导。出乎意料的是,我们在此表明,在人脐静脉内皮细胞(HUVECs)的原代培养物中,缺氧会抑制HO-1 mRNA的表达,但已知可模拟缺氧的氯化钴(CoCl₂)会使其增加。在所使用的培养条件下,缺氧或CoCl₂会增加HUVECs中缺氧诱导因子1的DNA结合和反式激活活性。因此,尽管缺氧诱导因子1被激活,但缺氧和钴对HO-1 mRNA表达显示出相反的作用。HO-1 mRNA的半衰期不受缺氧影响,但CoCl₂可使其显著延长。缺氧也会抑制人冠状动脉内皮细胞和星形胶质细胞中HO-1 mRNA的表达。HO-1表达的抑制可能代表某些细胞类型对缺氧的适应。

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