Kotani M, Kawashima I, Ozawa H, Ogura K, Ishizuka I, Terashima T, Tai T
Department of Tumor Immunology, Tokyo Metropolitan Institute of Medical Science, Japan.
Glycobiology. 1994 Dec;4(6):855-65. doi: 10.1093/glycob/4.6.855.
We previously described the differential distribution of major gangliosides (GM1, GD1a, GD1b, GT1b and GQ1b) in adult rat brain detected by specific antibodies (Kotani, M., Kawashima, I., Ozawa, I., Terashima, T. and Tai, T. Glycobiology, 3, 137-146, 1993). We report here the distribution of minor gangliosides in the adult rat brain by an immunofluorescence technique with mouse monoclonal antibodies (MAbs). Ten MAbs (GMR6, GMB28, GMR11, GMR19, GMR2, GMR7, GGR51, AMR10, NGR54 and NGR53) that specifically recognize GM3, GM2, GT1a, GD3, O-Acdisialoganglioside, GD2, GM1b, GM4, IV3NeuAc alpha-nLc4Cer and IV6NeuAc alpha-nLc4Cer, respectively, were used. Our study revealed that there is a cell type-specific expression of minor gangliosides, as well as major gangliosides, in the rat brain. In the cerebellar cortex, GM3 was expressed intensely in the white matter and slightly in the granular layer. GD3 was present in both the granular layer and the white matter, but not in the Purkinje cell layer or in the molecular layer. An O-Ac-disialoganglioside, which was suggested to be O-Ac-LD1, was detected exclusively in both the molecular layer and Purkinje cell layer. The presence of GD2 was restricted to the granular layer. GM4 was associated with some astrocytes, but not with myelin or oligodendrocytes. GM2, GT1a, GM1b, IV3NeuAc alpha-nLc4Cer and IV6NeuAc alpha-nLc4Cer gangliosides were not clearly detected in the cerebellar cortex. In other regions, such as cerebral cortex, hippocampal formation and spinal cord, the expression of the gangliosides was also highly localized to a specific cell type and layer.
我们之前描述过用特异性抗体检测成年大鼠脑中主要神经节苷脂(GM1、GD1a、GD1b、GT1b和GQ1b)的差异分布(小谷真、川岛一、小泽一、寺岛隆、太田哲。《糖生物学》,第3卷,第137 - 146页,1993年)。我们在此报告用小鼠单克隆抗体(MAbs)免疫荧光技术检测成年大鼠脑中次要神经节苷脂的分布情况。使用了10种单克隆抗体(GMR6、GMB28、GMR11、GMR19、GMR2、GMR7、GGR51、AMR10、NGR54和NGR53),它们分别特异性识别GM3、GM2、GT1a、GD3、O - 乙酰化双唾液酸神经节苷脂、GD2、GM1b、GM4、IV3NeuAcα - nLc4Cer和IV6NeuAcα - nLc4Cer。我们的研究表明,大鼠脑中次要神经节苷脂以及主要神经节苷脂存在细胞类型特异性表达。在小脑皮质中,GM3在白质中强烈表达,在颗粒层中微弱表达。GD3存在于颗粒层和白质中,但在浦肯野细胞层或分子层中不存在。一种被认为是O - 乙酰化LD1的O - 乙酰化双唾液酸神经节苷脂仅在分子层和浦肯野细胞层中检测到。GD2的存在局限于颗粒层。GM4与一些星形胶质细胞相关,但与髓磷脂或少突胶质细胞无关。在小脑皮质中未明确检测到GM2、GT1a、GM1b、IV3NeuAcα - nLc4Cer和IV6NeuAcα - nLc4Cer神经节苷脂。在其他区域,如大脑皮质、海马结构和脊髓,神经节苷脂的表达也高度定位于特定的细胞类型和层。