Udvadia A J, Köster R W, Skene J H
Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
Development. 2001 Apr;128(7):1175-82. doi: 10.1242/dev.128.7.1175.
A pivotal event in neural development is the point at which differentiating neurons become competent to extend long axons. Initiation of axon growth is equally critical for regeneration. Yet we have a limited understanding of the signaling pathways that regulate the capacity for axon growth during either development or regeneration. Expression of a number of genes encoding growth associated proteins (GAPs) accompanies both developmental and regenerative axon growth and has led to the suggestion that the same signaling pathways regulate both modes of axon growth. We have tested this possibility by asking whether a promoter fragment from a well characterized GAP gene, GAP-43, is sufficient to activate expression in both developing and regenerating neurons. We generated stable lines of transgenic zebrafish that express green fluorescent protein (GFP) under regulation of a 1 kb fragment of the rat GAP-43 gene, a fragment that contains a number of evolutionarily conserved elements. Analysis of GFP expression in these lines confirms that the rat 1 kb region can direct growth-associated expression of the transgene in differentiating neurons that extend long axons. Furthermore, this region supports developmental down-regulation of transgene expression which, like the endogenous gene, coincides with neuronal maturation. Strikingly, these same sequences are insufficient for directing expression in regenerating neurons. This finding suggests that signaling pathways regulating axon growth during development and regeneration are not the same. While these results do not exclude the possibility that pathways involved in developmental axon growth are also active in regenerative growth, they do indicate that signaling pathway(s) controlling activation of the GAP-43 gene after CNS injury differ in at least one key component from the signals controlling essential features of developmental axon growth.
神经发育中的一个关键事件是分化的神经元开始有能力延伸长轴突的那个点。轴突生长的起始对于再生同样至关重要。然而,我们对于在发育或再生过程中调节轴突生长能力的信号通路了解有限。许多编码生长相关蛋白(GAPs)的基因的表达伴随着发育性和再生性轴突生长,这使人提出相同的信号通路调节这两种轴突生长模式的观点。我们通过询问来自一个特征明确的GAP基因GAP - 43的启动子片段是否足以在发育中和再生中的神经元中激活表达,来检验这种可能性。我们构建了稳定的转基因斑马鱼品系,这些品系在大鼠GAP - 43基因的1 kb片段的调控下表达绿色荧光蛋白(GFP),该片段包含一些进化上保守的元件。对这些品系中GFP表达的分析证实,大鼠1 kb区域可以在延伸长轴突的分化神经元中指导转基因的生长相关表达。此外,该区域支持转基因表达的发育性下调,这与内源性基因一样,与神经元成熟同时发生。引人注目的是,这些相同的序列不足以指导再生神经元中的表达。这一发现表明,在发育和再生过程中调节轴突生长的信号通路并不相同。虽然这些结果不排除参与发育性轴突生长的通路在再生生长中也活跃的可能性,但它们确实表明,中枢神经系统损伤后控制GAP - 43基因激活的信号通路在至少一个关键成分上与控制发育性轴突生长基本特征的信号不同。