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Paper

Down-regulation of Jab1, HIF-1α, and VEGF by Moloney murine leukemia virus-ts1 infection: A possible cause of neurodegeneration

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Pages 239-251 | Received 16 Jan 2008, Accepted 28 Mar 2008, Published online: 10 Jul 2009
 

Abstract

Moloney murine leukemia virus–temperature sensitive (MoMuLV-ts1)-mediated neuronal death is a result of both loss of glial support and release of cytokines and neurotoxins from ts1-infected glial cells. Here the authors propose vascular endothelial growth factor (VEGF) down-regulation as another contributory factor in neuronal degeneration induced by ts1 infection. To determine how ts1 affects VEGF expression in ts1-infected brain, the authors examined the expression of several proteins that are important in regulating the expression of VEGF. The authors found significant decreases in Jun-activating domain-binding protein 1 (Jab1), hypoxia-inducible factor (HIF)-1α, and VEGF levels and increases in p53 protein levels in ts1-infected brains compared to noninfected control brains. The authors suggest that a decrease Jab1 expression in ts1 infection leads to accumulation of p53, which binds to HIF-1α to accelerate its degradation. A rapid degradation of HIF-1α leads to decreased VEGF production and secretion. Considering that endothelial cells are the most conspicuous in virus replication and production in ts1 infection, but are not killed by the infection, the authors examined the expression of these proteins using infected and noninfected mouse cerebrovascular endothelial (CVE) cells. The ts1- infected CVE cells showed decreased Jab1, HIF-1α, and VEGF mRNA and protein levels and increased p53 protein levels compared with noninfected cells, consistent with the results found in vivo. These results confirm that ts1 infection results in insufficient secretion of VEGF from endothelial cells and may result in decreased neuroprotection. This study suggested that ts1-mediated neuropathology in mice may result from changes in expression and activity of Jab1, p53, and HIF-1α, with a final target on VEGF expression and neuronal degeneration.

This work was supported by National Institutes of Health grants 5R01 MH071583 18 and 2R01 NS043984 05 A1 awarded to P. K. Y. Wong. The authors are grateful to Dr. JaneWelsh for providing the BALB/c mice CVE cell line. They thank Xueyi Xie for technical assistance.

This article is not subject to US copyright law.

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