Morsink M C, Joëls M, Sarabdjitsingh R A, Meijer O C, De Kloet E R, Datson N A
Division of Medical Pharmacology, Leiden/Amsterdam Center for Drug Research, Amsterdam, the Netherlands.
J Neurochem. 2006 Nov;99(4):1282-98. doi: 10.1111/j.1471-4159.2006.04187.x. Epub 2006 Oct 2.
The aim of the current study was (i) to examine the overlap in the pattern of glucocorticoid receptor (GR)-mediated transcriptional responses between different neuronal substrates and (ii) to assess the nature of these responses by differentiating between primary and downstream GR-responsive genes. For this purpose, nerve growth factor-differentiated catecholaminergic PC12 cells were used in which endogenous GRs were activated briefly with a high dose of corticosterone followed by gene expression profiling 1 and 3 h afterwards using Affymetrix GeneChips. The results revealed a strikingly similar temporal pattern to that which was reported previously in hippocampus, with only down-regulated genes 1 h after GR activation and the majority of genes up-regulated 3 h after GR activation. Real-time quantatitive PCR of transcripts in cycloheximide-treated cells showed that all five GR-responsive genes selected from the 1-h time point were primary responsive, whereas all four GR-responsive genes selected from the 3-h time point were downstream responsive. At the level of individual genes, the overlap with the previously generated hippocampal data sets was small, illustrating the cell-type specifity of GR-mediated genomic responses. Finally, we identified a number of interesting genes, such as SWI/SNF, synaptosomal-associated protein 25 and certain Rab proteins which may play a role in the effects of glucocorticoids on catecholaminergic neuronal functioning.
(i)检查不同神经元底物之间糖皮质激素受体(GR)介导的转录反应模式的重叠情况;(ii)通过区分初级和下游GR反应基因来评估这些反应的性质。为此,使用了经神经生长因子分化的儿茶酚胺能PC12细胞,先用高剂量皮质酮短暂激活其内源性GR,然后在1小时和3小时后使用Affymetrix基因芯片进行基因表达谱分析。结果显示出与先前在海马体中报道的惊人相似的时间模式,GR激活后1小时只有基因下调,而GR激活后3小时大多数基因上调。对用放线菌酮处理的细胞中的转录本进行实时定量PCR分析表明,从1小时时间点选择的所有五个GR反应基因都是初级反应基因,而从3小时时间点选择的所有四个GR反应基因都是下游反应基因。在单个基因水平上,与先前生成的海马体数据集的重叠很小,这说明了GR介导的基因组反应的细胞类型特异性。最后,我们鉴定出了一些有趣的基因,如SWI/SNF、突触体相关蛋白25和某些Rab蛋白,它们可能在糖皮质激素对儿茶酚胺能神经元功能的影响中发挥作用。