Hypoxia-inducible factor-1 alpha regulates prion protein expression to protect against neuron cell damage

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• 作者：Jae-Kyo Jeong¹ ; Jae-Suk Seo¹ ; Myung-Hee Moon ; You-Jin Lee ; Jae-Won Seol ; Sang-Youel Park ; ^{sypark@chonbuk.ac.kr}
• 关键词：prp106-126 ; Neuron cell ; Hypoxia ; HIF-1伪 ; PrPC
• 刊名：Neurobiology of Aging
• 出版年：2012
• 期刊代码：202_01974580
• 类别：med
• 出版时间：May, 2012
• 卷：33
• 期：5
• 页码：1006.e1-1006.e10
• 文件大小：2445 K

摘要

The human prion protein fragment, PrP (106-126), may contain a majority of the pathological features associated with the infectious scrapie isoform of PrP, known as PrP^Sc. Based on our previous findings that hypoxia protects neuronal cells from PrP (106-126)-induced apoptosis and increases cellular prion protein (PrP^C) expression, we hypothesized that hypoxia-related genes, including hypoxia-inducible factor-1 alpha (HIF-1伪), may regulate PrP^C expression and that these genes may be involved in prion-related neurodegenerative diseases. Hypoxic conditions are known to elicit cellular responses designed to improve cell survival through adaptive processes. Under normoxic conditions, a deferoxamine-mediated elevation of HIF-1伪 produced the same effect as hypoxia-inhibited neuron cell death. However, under hypoxic conditions, doxorubicin-suppressed HIF-1伪 attenuated the inhibitory effect on neuron cell death mediated by PrP (106-126). Knock-down of HIF-1伪 using lentiviral short hairpin (sh) RNA-induced downregulation of PrP^C mRNA and protein expression under hypoxic conditions, and sensitized neuron cells to prion peptide-mediated cell death even in hypoxic conditions. In PrP^C knockout hippocampal neuron cells, hypoxia increased the HIF-1伪 protein but the cells did not display the inhibitory effect of prion peptide-induced neuron cell death. Adenoviruses expressing the full length Prnp gene (Ad-Prnp) were utilized for overexpression of the Prnp gene in PrP^C knockout hippocampal neuron cells. Adenoviral transfection of PrP^C knockout cells with Prnp resulted in the inhibition of prion peptide-mediated cell death in these cells. This is the first report demonstrating that expression of normal PrP^C is regulated by HIF-1伪, and PrP^C overexpression induced by hypoxia plays a pivotal role in hypoxic inhibition of prion peptide-induced neuron cell death. These results suggest that hypoxia-related genes, including HIF-1伪, may be involved in the pathogenesis of prion-related diseases and as such may be a therapeutic target for prion-related neurodegenerative diseases.