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发育中的大鼠小脑浦肯野细胞原位表达GD3神经节苷脂。

Expression of GD3 ganglioside by developing rat cerebellar Purkinje cells in situ.

作者信息

Reynolds R, Wilkin G P

机构信息

Department of Biochemistry, Imperial College of Science and Technology, London, England.

出版信息

J Neurosci Res. 1988 Jul;20(3):311-9. doi: 10.1002/jnr.490200305.

DOI:10.1002/jnr.490200305
PMID:3225869
Abstract

GD3 is a major ganglioside of the immature vertebrate CNS, and its expression is suggested to be characteristic of immature neuroectodermal cells. Using immunocytochemistry on cryostat sections of developing rat cerebellum with a monoclonal antibody specific for GD3, we have found that GD3 begins to be expressed on the plasma membrane of Purkinje cell bodies and dendrites beginning at postnatal day 7. Staining became brighter as the dendritic tree of the cells enlarged. As the Purkinje cells began to mature in different folia, they became GD3+, until by 15 days postnatal all Purkinje cells were GD3+. Positive staining of the dendritic tree was still present in the adult cerebellum. Using a monoclonal antibody 7-8D2, which recognizes cerebellar granule cells and their axons (the parallel fibres), and polyclonal antibodies against a synaptic vesicle component synaptophysin, double-immunofluorescence staining together with anti-GD3 antibodies suggested that the appearance of GD3 immunoreactivity did not correlate either with the ingrowth of parallel fibres or the presence of their synapses on Purkinje cell dendrites. However, comparison with earlier morphological studies showed that the appearance of GD3 immunoreactivity correlated well with the formation of climbing fibre synapses on Purkinje cell dendrites and the onset of the rapid expansion of the dendritic tree. These results are in keeping with the idea that elevated GD3 concentrations are found in certain cell types during periods of rapid growth or high metabolic activity but also show that this is not only restricted to immature cells.

摘要

GD3是未成熟脊椎动物中枢神经系统的主要神经节苷脂,其表达被认为是未成熟神经外胚层细胞的特征。使用针对GD3的单克隆抗体对发育中的大鼠小脑冷冻切片进行免疫细胞化学研究,我们发现GD3从出生后第7天开始在浦肯野细胞体和树突的质膜上表达。随着细胞树突的扩大,染色变得更亮。随着不同小叶中的浦肯野细胞开始成熟,它们变成GD3阳性,直到出生后15天所有浦肯野细胞都为GD3阳性。在成年小脑中仍存在树突的阳性染色。使用识别小脑颗粒细胞及其轴突(平行纤维)的单克隆抗体7-8D2,以及针对突触小泡成分突触素的多克隆抗体,与抗GD3抗体一起进行双免疫荧光染色表明,GD3免疫反应性的出现与平行纤维的长入或它们在浦肯野细胞树突上的突触的存在均无关。然而,与早期形态学研究的比较表明,GD3免疫反应性的出现与浦肯野细胞树突上攀缘纤维突触的形成以及树突快速扩展的开始密切相关。这些结果与以下观点一致,即在快速生长或高代谢活动期间某些细胞类型中发现GD3浓度升高,但也表明这不仅限于未成熟细胞。

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