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慢性缺氧时大鼠脑内缺氧诱导因子-1α的表达

Expression of hypoxia-inducible factor-1alpha in the brain of rats during chronic hypoxia.

作者信息

Chávez J C, Agani F, Pichiule P, LaManna J C

机构信息

Department of Anatomy, Case Western Reserve University, School of Medicine, Cleveland, Ohio 44106, USA.

出版信息

J Appl Physiol (1985). 2000 Nov;89(5):1937-42. doi: 10.1152/jappl.2000.89.5.1937.

Abstract

Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that regulates adaptive responses to the lack of oxygen in mammalian cells. HIF-1 consists of two proteins, HIF-1alpha and HIF-1beta. HIF-1alpha accumulates under hypoxic conditions, whereas HIF-1beta is constitutively expressed. HIF-1alpha and HIF-1beta expression were measured during adaptation to hypobaric hypoxia (0.5 atm) in rat cerebral cortex. Western blot analyses indicated that HIF-1alpha rapidly accumulated during the onset of hypoxia and did not fall for 14 days but fell to normal by 21 days despite the continuous low arterial oxygen tension. Immunostaining showed that neurons, astrocytes, ependymal cells, and possibly endothelial cells were the cell types expressing HIF-1alpha. Genes with hypoxia-responsive elements were activated under these conditions, as evidenced by elevated vascular endothelial growth factor and glucose transporter-1 mRNA levels. When 21-day-adapted rats were exposed to a more severe hypoxic challenge (8% oxygen), HIF-1alpha accumulated again. On the basis of these results, we speculate that the vascular remodeling and metabolic changes triggered during prolonged hypoxia are capable of restoring normal tissue oxygen levels.

摘要

缺氧诱导因子-1(HIF-1)是一种转录因子,可调节哺乳动物细胞对缺氧的适应性反应。HIF-1由两种蛋白质组成,即HIF-1α和HIF-1β。HIF-1α在缺氧条件下会积累,而HIF-1β则持续表达。在大鼠大脑皮层适应低压缺氧(0.5个大气压)的过程中,对HIF-1α和HIF-1β的表达进行了检测。蛋白质免疫印迹分析表明,HIF-1α在缺氧开始时迅速积累,在14天内都没有下降,但尽管动脉血氧张力持续较低,到21天时却降至正常水平。免疫染色显示,神经元、星形胶质细胞、室管膜细胞以及可能的内皮细胞是表达HIF-1α的细胞类型。在这些条件下,具有缺氧反应元件的基因被激活,血管内皮生长因子和葡萄糖转运蛋白-1的mRNA水平升高证明了这一点。当适应21天的大鼠受到更严重的缺氧挑战(8%氧气)时,HIF-1α再次积累。基于这些结果,我们推测长时间缺氧期间引发的血管重塑和代谢变化能够恢复正常的组织氧水平。

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