Boeshore Kristen L, Schreiber Rebecca C, Vaccariello Stacey A, Sachs Hilary Hyatt, Salazar Rafael, Lee Junghee, Ratan Rajiv R, Leahy Patrick, Zigmond Richard E
Department of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
J Neurobiol. 2004 May;59(2):216-35. doi: 10.1002/neu.10308.
Neurons of the peripheral nervous system are capable of extensive regeneration following axonal injury. This regenerative response is accompanied by changes in gene expression in axotomized neurons and associated nonneuronal cells. In the sympathetic nervous system, a few of the genes affected by axonal injury have been identified; however, a broad sampling of genes that could reveal additional and unexpected changes in expression has been lacking. We have used DNA microarray technology to study changes in gene expression within 48 h of transecting the postganglionic trunks of the adult rat superior cervical ganglion (SCG). The expression of more than 200 known genes changed in the ganglion, most of these being genes not previously associated with the response to injury. In contrast, only 10 genes changed following transection of the preganglionic cervical sympathetic trunk. Real-time RT-PCR analysis verified the upregulation of a number of the axotomy-induced genes, including activating transcription factor-3 (ATF-3), arginase I (arg I), cardiac ankyrin repeat protein, galanin, osteopontin, pituitary adenylate cyclase-activating polypeptide (PACAP), parathyroid hormone-related peptide, and UDP-glucoronosyltransferase. Arg I mRNA and protein were shown to increase within neurons of the axotomized SCG. Furthermore, increases in the levels of putrescine and spermidine, a diamine and polyamine produced downstream of arg I activity, were also detected in the axotomized SCG. Our results identified many candidate genes to be studied in the context of peripheral nerve regeneration. In addition, the data suggest a potential role for putrescine and spermidine, acting downstream of arg I, in the regenerative process.
外周神经系统的神经元在轴突损伤后能够进行广泛的再生。这种再生反应伴随着轴突切断的神经元和相关非神经元细胞中基因表达的变化。在交感神经系统中,已经鉴定出一些受轴突损伤影响的基因;然而,缺乏对可能揭示表达中额外和意外变化的基因进行广泛采样。我们使用DNA微阵列技术研究成年大鼠颈上神经节(SCG)节后干横断后48小时内基因表达的变化。神经节中200多个已知基因的表达发生了变化,其中大多数是以前与损伤反应无关的基因。相比之下,节前颈交感干横断后只有10个基因发生了变化。实时RT-PCR分析证实了许多轴突切断诱导基因的上调,包括激活转录因子-3(ATF-3)、精氨酸酶I(arg I)、心脏锚蛋白重复蛋白、甘丙肽、骨桥蛋白、垂体腺苷酸环化酶激活多肽(PACAP)、甲状旁腺激素相关肽和UDP-葡萄糖醛酸基转移酶。Arg I mRNA和蛋白在轴突切断的SCG神经元内增加。此外,在轴突切断的SCG中也检测到腐胺和亚精胺水平的增加,腐胺和亚精胺是arg I活性下游产生的二胺和多胺。我们的结果鉴定出许多在外周神经再生背景下有待研究的候选基因。此外,数据表明腐胺和亚精胺在再生过程中可能在arg I下游发挥作用。