Borgas Diana L, Gao Jin-Song, Tong Ming, de la Monte Suzanne M
Liver Research Center, Divisions of Gastroenterology and Neuropathology, and Departments of Medicine, Pathology, Neurology, and Neurosurgery, Rhode Island Hospital and the Warren Alpert Medical School of Brown University, Providence, RI., USA.
Liver Cancer. 2015 Sep;4(3):139-53. doi: 10.1159/000367731. Epub 2015 Jun 5.
Abundant expression of aspartyl-(asparaginyl)-β-hydroxylase (AAH) correlates with infiltrative growth of hepatocellular carcinoma (HCC). Herein, we examine the role of phosphorylation in relation to AAH's protein expression, hydroxylase activity, promotion of cell motility, and activation of Notch signaling in human Huh7 hepatoma cells. Predicted glycogen synthase kinase-3β (GSK-3β), protein kinase A (PKA), protein kinase C (PKC), and casein kinase 2 (CK2) phosphorylation sites encoded by human AAH cDNA were ablated by S/T→A site-directed mutagenesis using N-Myc-tagged constructs in which gene expression was controlled by a cytomegalovirus promoter. Functional consequences were assessed in transiently transfected Huh7 cells. Cells transfected with wildtype AAH had significantly increased AAH expression, catalytic activity, HES-1 expression, and directional motility relative to controls. Single phosphorylation site mutations in the C-terminus largely abrogated these effects and further inhibited catalytic activity relative to that in cells transfected with empty vector, whereas the effects of single point mutations within the N-terminus were more varied. In contrast, AAH cDNAs carrying multiple phosphorylation site mutations exhibited wildtype levels of AAH catalytic activity suggesting that the effects of AAH phosphorylation are complex and non-uniform. AAH expression and function can be modulated by direct phosphorylation of the protein. These findings suggest additional strategies for inhibiting infiltrative growth of HCC.
天冬氨酰-(天冬酰胺基)-β-羟化酶(AAH)的高表达与肝细胞癌(HCC)的浸润性生长相关。在此,我们研究了磷酸化在人Huh7肝癌细胞中与AAH的蛋白表达、羟化酶活性、促进细胞运动以及Notch信号激活之间的关系。使用由巨细胞病毒启动子控制基因表达的N-Myc标签构建体,通过S/T→A定点诱变消除了人AAH cDNA编码的预测糖原合酶激酶-3β(GSK-3β)、蛋白激酶A(PKA)、蛋白激酶C(PKC)和酪蛋白激酶2(CK2)磷酸化位点。在瞬时转染的Huh7细胞中评估功能后果。与对照相比,转染野生型AAH的细胞具有显著增加的AAH表达、催化活性、HES-1表达和定向运动性。C末端的单个磷酸化位点突变在很大程度上消除了这些效应,并且相对于空载体转染的细胞进一步抑制了催化活性,而N末端内单点突变的效应则更为多样。相反,携带多个磷酸化位点突变的AAH cDNA表现出野生型水平的AAH催化活性,这表明AAH磷酸化的效应是复杂且不均匀的。AAH的表达和功能可通过该蛋白的直接磷酸化进行调节。这些发现提示了抑制HCC浸润性生长的其他策略。