Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, S7N 5B4, Canada.
J Neurooncol. 2012 Sep;109(3):485-501. doi: 10.1007/s11060-012-0927-z. Epub 2012 Jul 15.
Cells from medulloblastoma lines do not contain detectable amounts of the basic leucine-zipper protein Zhangfei. However, we have previously shown that expression of this protein in cells of the ONS-76 and UW228 medulloblastoma lines causes the cells to stop growing and develop processes that resemble neurites. Our objective was to determine the molecular mechanisms by which Zhangfei influences ONS-76 cells. We infected ONS-76 cells with adenovirus vectors expressing either Zhangfei or the control protein LacZ and then compared the following parameters in Zhangfei and LacZ-expressing cells: (a) markers of apoptosis, autophagy and macropinocytosis, (b) transcripts for genes involved in neurogenesis and apoptosis, (c) phosphorylation of peptide targets of selected cellular protein kinases, and (d) activation of transcription factors. Zhangfei-expressing cells appeared to succumb to apoptosis. Increased staining for autophagic vesicles and upregulated expression of autophagy response genes in these cells indicated that they were undergoing autophagy, possibly associated with apoptosis. Within our analysis, patterns of gene expression and phosphorylation-mediated signal transduction activity in Zhangfei-expressing cells indicated that the mitogen-activated protein kinase (MAPK) pathway was active. In addition, we found that the transcription factor Brn3a as well as factors implicated in differentiation were also active in Zhangfei-expressing cells. We tested the hypothesis that Zhangfei enhances the expression of Brn3a, a known inducer of TrkA, the high-affinity receptor for nerve growth factor (NGF). TrkA then engages NGF in an autocrine manner triggering the MAPK pathway and leading to differentiation of ONS-76 cells into neuron and glia-like cells-a process that eventually brings about cell death. We showed that: (a) Zhangfei could enhance transcription from the isolated Brn3a promoter, (b) ONS-76 cells produced NGF and (c) antibodies against NGF and inhibitors of TrkA and selected components of the MAPK pathway could partially restore the growth of Zhangfei-expressing ONS-76 cells.
髓母细胞瘤系细胞中不含有可检测量的基本亮氨酸拉链蛋白张飞。然而,我们先前的研究表明,在 ONS-76 和 UW228 髓母细胞瘤系细胞中表达该蛋白可导致细胞停止生长并发育出类似于神经突的突起。我们的目的是确定张飞蛋白影响 ONS-76 细胞的分子机制。我们用表达张飞或对照蛋白 LacZ 的腺病毒载体感染 ONS-76 细胞,然后比较表达张飞和 LacZ 的细胞的以下参数:(a) 凋亡、自噬和巨胞饮的标志物,(b) 参与神经发生和凋亡的基因的转录物,(c) 选定细胞蛋白激酶的肽靶标磷酸化,和(d) 转录因子的激活。表达张飞的细胞似乎容易凋亡。这些细胞中自噬小体的染色增加和自噬反应基因的上调表明它们正在经历自噬,可能与凋亡有关。在我们的分析中,表达张飞的细胞中的基因表达和磷酸化介导的信号转导活性模式表明丝裂原活化蛋白激酶 (MAPK) 途径是活跃的。此外,我们发现转录因子 Brn3a 以及与分化相关的因子也在表达张飞的细胞中活跃。我们检验了这样一种假说,即张飞增强了已知诱导 TrkA 的转录因子 Brn3a 的表达,TrkA 是神经生长因子 (NGF) 的高亲和力受体。然后,TrkA 通过自分泌方式与 NGF 结合,触发 MAPK 途径,导致 ONS-76 细胞向神经元和神经胶质样细胞分化——这一过程最终导致细胞死亡。我们表明:(a) 张飞可以增强分离的 Brn3a 启动子的转录,(b) ONS-76 细胞产生 NGF,和(c) NGF 抗体以及 TrkA 和 MAPK 途径的选定成分的抑制剂可以部分恢复表达张飞的 ONS-76 细胞的生长。