Przyborski S A, Cambray-Deakin M A
Department of Biomedical Science, University of Sheffield, UK.
Brain Res Mol Brain Res. 1994 Sep;25(3-4):273-85. doi: 10.1016/0169-328x(94)90163-5.
GAP-43 is a growth-associated protein that has been implicated in the developmental outgrowth of axons. We have examined the profile of GAP-43 levels in rat cerebellar granule cells during their development in vitro. During the first 1-2 days after plating, the majority of cells expressed neurites and after 8 days a complex neuronal network had developed. In situ hybridization studies showed that GAP-43 mRNA levels rapidly increased to peak at 1-2 days and gradually returned to initial values after 7-8 days. Analysis of GAP-43 protein levels followed a similar transient profile. Initially, granule cell perikarya and structures associated with neuritogenesis all displayed GAP-43 immunoreactivity. In older cultures, perikaryal labelling was lost after 10 days whilst process staining decreased more gradually. During the first 48 hours detailed analysis of GAP-43 mRNA revealed two populations of granule cells. It was suggested that cells with significant label originated from the external germinal layer which displays much GAP-43 mRNA in cerebellar sections. Cells with little or no GAP-43, however, probably originated from the internal granular layer since this region displayed no specific labelling. Granule cells within clumps expressed more GAP-43 mRNA compared to isolated cells perhaps indicating cell-cell regulation of expression. These results describe the transient rise in GAP-43 protein and mRNA levels expressed by developing cerebellar granule cell neurons in vitro and provide further evidence for the role GAP-43 plays during neuritogenesis.
GAP - 43是一种与生长相关的蛋白,与轴突的发育性生长有关。我们已经检测了大鼠小脑颗粒细胞在体外发育过程中GAP - 43水平的变化情况。在接种后的最初1 - 2天,大多数细胞长出了神经突,8天后形成了复杂的神经网络。原位杂交研究表明,GAP - 43 mRNA水平在1 - 2天迅速上升至峰值,7 - 8天后逐渐恢复到初始值。GAP - 43蛋白水平的分析呈现出类似的短暂变化情况。最初,颗粒细胞的胞体以及与神经突形成相关的结构都显示出GAP - 43免疫反应性。在较老的培养物中,10天后胞体标记消失,而突起染色的减少则较为缓慢。在最初的48小时内,对GAP - 43 mRNA的详细分析揭示了两种颗粒细胞群体。有人认为,标记明显的细胞起源于外生发层,该层在小脑切片中显示有大量GAP - 43 mRNA。然而,GAP - 43很少或没有的细胞可能起源于内颗粒层,因为该区域没有显示出特异性标记。与分离的细胞相比,细胞团内的颗粒细胞表达更多的GAP - 43 mRNA,这可能表明存在细胞间的表达调控。这些结果描述了体外培养的发育中小脑颗粒细胞神经元中GAP - 43蛋白和mRNA水平的短暂升高,并为GAP - 43在神经突形成过程中所起的作用提供了进一步的证据。