Unidad de Investigación Médica en Epidemiología Clínica, UMAE, Hospital de Especialidades, CMNO, IMSS, Mexico.
J Neuroimmunol. 2011 Sep 15;238(1-2):12-8. doi: 10.1016/j.jneuroim.2011.06.001. Epub 2011 Jul 31.
Hypoxia-inducible factor-1 alpha (HIF-1α) is a master transcription factor that regulates the response to hypoxia and ischemia and induces the expression of various genes, including vascular endothelial growth factor (VEGF) and erythropoietin (EPO). This study shows the systemic response of increased HIF-1α, EPO, and VEGF mRNA and protein. In addition, VEGF expression was increased in neurons and over-expressed in glial cells in a model of neuroexcitotoxicity in the hippocampus, in which rats were neonatally exposed to high glutamate concentrations. Simultaneous increases in HIF-1α, EPO and VEGF mRNA in peritoneal macrophages were also observed. Our study is consistent with the hypothesis that these genes exert a protective effect in response to neurotoxicity.
缺氧诱导因子-1α(HIF-1α)是一种主转录因子,可调节对缺氧和缺血的反应,并诱导各种基因的表达,包括血管内皮生长因子(VEGF)和促红细胞生成素(EPO)。本研究显示了系统反应中 HIF-1α、EPO 和 VEGF mRNA 和蛋白水平的增加。此外,在海马的神经兴奋性毒性模型中,新生大鼠暴露于高谷氨酸浓度时,神经元中 VEGF 的表达增加,胶质细胞中过度表达。同时观察到腹腔巨噬细胞中 HIF-1α、EPO 和 VEGF mRNA 水平的增加。我们的研究支持这样一种假设,即这些基因在应对神经毒性时发挥保护作用。