Department of Chemistry, University of Western Ontario, London, Ontario, Canada.
Neurosci Lett. 2011 Apr 20;494(1):80-5. doi: 10.1016/j.neulet.2011.02.061. Epub 2011 Mar 6.
The p53 transcription factor is involved in cell cycle, apoptosis and differentiation. However, the mechanism of p53 mediated differentiation is not fully understood. Here, we show that recently discovered dual oxidase maturation factor 1 (DUOXA1), which was implicated in neuronal differentiation, is regulated by p53 and may be an important factor in neuronal differentiation. We show that DUOXA1 is highly expressed in mouse neuronal stem cells with intensive nuclear localization. A strong interaction between DUOXA1 and p53 is observed in undifferentiated cells and declines in terminally differentiated neurons. Overexpressed p53 induces marked DUOXA1 expression in P19 cells and intensifies neuronal differentiation in the presence of retinoic acid, which suggests that p53 and DUOXA1 possess a neural differentiation potential. At day 3 of retinoic acid induced differentiation when cells showed a typical morphology of neuronal progenies, CD133 expression was down-regulated. The expression level of CD133 was significantly decreased in p53 over-expressing cells and was accompanied by a substantial increase in the expression level of neurofilament. In conclusion, DUOXA1 is a novel p53-regulated neurogenic factor involved in p53 dependent neuronal differentiation.
p53 转录因子参与细胞周期、凋亡和分化。然而,p53 介导的分化机制尚未完全阐明。在这里,我们发现最近发现的双氧化酶成熟因子 1(DUOXA1),其与神经元分化有关,受 p53 调控,可能是神经元分化的重要因素。我们发现 DUOXA1 在具有强烈核定位的小鼠神经元干细胞中高度表达。在未分化细胞中观察到 DUOXA1 和 p53 之间的强烈相互作用,并在终末分化神经元中下降。过表达的 p53 在 P19 细胞中诱导明显的 DUOXA1 表达,并在视黄酸存在下增强神经元分化,这表明 p53 和 DUOXA1 具有神经分化潜能。在视黄酸诱导分化的第 3 天,当细胞呈现出神经元前体的典型形态时,CD133 的表达下调。在过表达 p53 的细胞中,CD133 的表达水平显著降低,同时神经丝的表达水平显著增加。总之,DUOXA1 是一种新的 p53 调节的神经发生因子,参与 p53 依赖性神经元分化。