Department of Oncology, Graduate School of Pharmaceutical Science, Nagoya City University, Nagoya, Japan.
J Biochem. 2012 Jun;151(6):611-20. doi: 10.1093/jb/mvs033. Epub 2012 Mar 26.
Neutral ceramidase (NCDase) is considered to be a critical enzyme for controlling the turnover of ceramide, an important bioactive lipid, which determines cell's fate. All-trans retinoic acid (ATRA) has been reported to induce neuronal differentiation and cell-cycle arrest [Lopez-Carballo, Moreno, Masia, Perez, and Barettino (Activation of the phosphatidylinositol 3-kinase/Akt signalling pathway by retinoic acid is required for neural differentiation of SH-SY5Y human neuroblastoma cells. J Biol Chem 2002:277:25297-304.)]. In this study, we observed that ATRA-induced cellular ceramide accumulation, cell-growth arrest and differentiation accompanied with down-regulation of NCDase in SH-SY5Y cells, without a decrease in sphingosine or sphingosine 1-phosphate. We examined whether the down-regulation of NCDase was involved in the increase in ceramide and cell differentiation. ATRA was found to down-regulate mRNA, protein and the enzyme activity of NCDase. Interestingly, GATA-2 was also decreased with ATRA treatment, and experiments using its expression vector and siRNA and chromatin immunoprecipitation assay demonstrated GATA-2 acted as transcription-factor of NCDase gene expression. By establishing stable transfectants with decreased NCDase expression and activity, we clarified the significance of NCDase down-regulation for ATRA-induced neuronal differentiation. Those sub-clones showed both increased cellular ceramide and reduced cell growth as well as neuronal differentiation phenotypes. These results demonstrate that down-regulation of NCDase through ATRA-induced GATA-2 decrease plays an important role in induction of ceramide accumulation and neuronal differentiation in SH-SY5Y cells.
中性鞘氨醇酶(NCDase)被认为是控制神经酰胺(一种重要的生物活性脂质)周转的关键酶,而神经酰胺决定细胞的命运。全反式视黄酸(ATRA)已被报道可诱导神经元分化和细胞周期停滞[Lopez-Carballo、Moreno、Masia、Perez 和 Barettino(视黄酸激活磷脂酰肌醇 3-激酶/Akt 信号通路对于 SH-SY5Y 人神经母细胞瘤细胞的神经分化是必需的。J Biol Chem 2002:277:25297-304.)]。在本研究中,我们观察到 ATRA 诱导的细胞神经酰胺积累、细胞生长停滞和分化伴随着 SH-SY5Y 细胞中 NCDase 的下调,而鞘氨醇或鞘氨醇 1-磷酸没有减少。我们检查了 NCDase 的下调是否参与神经酰胺的增加和细胞分化。发现 ATRA 下调 NCDase 的 mRNA、蛋白和酶活性。有趣的是,GATA-2 也随着 ATRA 处理而减少,使用其表达载体和 siRNA 以及染色质免疫沉淀测定实验表明 GATA-2 作为 NCDase 基因表达的转录因子。通过建立表达 NCDase 减少的稳定转染子和活性,我们阐明了 NCDase 下调对 ATRA 诱导的神经元分化的重要意义。这些亚克隆表现出细胞神经酰胺增加和细胞生长减少以及神经元分化表型。这些结果表明,通过 ATRA 诱导的 GATA-2 减少下调 NCDase 在 SH-SY5Y 细胞中神经酰胺积累和神经元分化的诱导中发挥重要作用。