Department of Anatomy, Shinshu University, School of Medicine, Matsumoto, Nagano, Japan.
Gene. 2011 Apr 1;475(1):1-9. doi: 10.1016/j.gene.2010.11.014. Epub 2010 Dec 9.
Although amyloid precursor protein (APP) plays a central role in Alzheimer's disease, the physiological functions of this protein have yet to be fully elucidated. As previously reported, we established an embryonic carcinoma P19 cell line expressing the intracellular domain of APP (AICD). While neurons were differentiated from these cell lines with retinoic acid treatment, expression of AICD induced neuron-specific apoptosis. As the first step to identify the genes involved in this process, we evaluated AICD-induced changes in gene expression through cell death. The levels of expression of 41,256 transcripts were monitored by DNA microarray analysis. The expression of 277 genes showed up-regulation by more than 10-fold in the presence of AICD. Conversely, the expression of 341 genes showed down-regulation to less than one-tenth of the original level. Reverse transcription-polymerase chain reaction of 17 selected genes showed excellent agreement with the microarray results. These results suggest that AICD induces dynamic changes in gene expression, which may be closely correlated with AICD-induced neuron-specific apoptosis.
尽管淀粉样前体蛋白 (APP) 在阿尔茨海默病中起着核心作用,但该蛋白质的生理功能尚未完全阐明。如前所述,我们建立了表达 APP 细胞内结构域 (AICD) 的胚胎癌细胞系 P19。在用维甲酸处理将这些细胞系分化为神经元时,AICD 的表达诱导神经元特异性凋亡。作为鉴定该过程中涉及的基因的第一步,我们通过细胞死亡评估了 AICD 诱导的基因表达变化。通过 DNA 微阵列分析监测了 41256 个转录物的表达水平。在存在 AICD 的情况下,有 277 个基因的表达上调了 10 倍以上。相反,341 个基因的表达下调到原始水平的十分之一以下。对 17 个选定基因的逆转录聚合酶链反应与微阵列结果具有极好的一致性。这些结果表明,AICD 诱导基因表达的动态变化,这可能与 AICD 诱导的神经元特异性凋亡密切相关。