Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
Cell Biochem Funct. 2013 Jul;31(5):400-11. doi: 10.1002/cbf.2914. Epub 2012 Oct 11.
Growth-associated protein 43 (GAP-43), a novel axonal phosphoprotein, is originally identified as a growth-cone-specific protein of developing neurons in vitro. The expression of GAP-43 is also shown to be up-regulated concomitant with increased synaptic plasticity in the brains in vivo, but how GAP-43 is concerned with synaptic plasticity is not well understood. In the present study, therefore, we aimed to elucidate subcellular localization of GAP-43 as culture development of rat hippocampal neurons. Western blotting showed that the expression of GAP-43 in the cerebral and hippocampal tissues was prominently high at postnatal days 14 and 21 or the active period of synaptogenesis. Double-labelling immunohistochemistry with an axonal marker Tau revealed that the immunoreactivity of GAP-43 was seen throughout axons of cultured hippocampal neurons but stronger at axonal puncta of developing neurons than axonal processes. Double-labelling immunohistochemistry with presynaptic terminal markers of synapsin and synaptotagmin revealed that the immunoreactivity of GAP-43 was observed mostly at weak synapsin- and synaptotagmin-positive puncta rather than strong ones. The quantitative analysis of immunofluorescent intensity showed a clear inverse correlation between GAP-43 and either synapsin or synaptotagmin expression. These data indicate that GAP-43 is highly expressed at immature growing axonal terminals and its expression is decreased along with the maturation of synaptogenesis.
生长相关蛋白 43(GAP-43)是一种新型的轴突磷酸蛋白,最初在体外被鉴定为发育神经元中的生长锥特异性蛋白。体内研究表明,GAP-43 的表达也伴随着突触可塑性的增加而上调,但 GAP-43 如何与突触可塑性有关尚不清楚。因此,在本研究中,我们旨在阐明 GAP-43 的亚细胞定位与大鼠海马神经元培养发育的关系。Western blot 分析显示,GAP-43 在大脑和海马组织中的表达在出生后第 14 天和第 21 天或突触发生的活跃期明显较高。用轴突标志物 Tau 进行双重免疫荧光染色显示,GAP-43 的免疫反应性可见于培养的海马神经元的整个轴突中,但在发育神经元的轴突突处比轴突过程中更强。用突触前末端标志物突触素和突触结合蛋白的双重免疫荧光染色显示,GAP-43 的免疫反应性主要见于弱突触素和突触结合蛋白阳性的突处,而不是强的突处。免疫荧光强度的定量分析显示,GAP-43 与突触素或突触结合蛋白的表达呈明显的负相关。这些数据表明,GAP-43 在未成熟的生长轴突末端高度表达,其表达随着突触发生的成熟而降低。