We previously described the differential distribution of major ganglio
sides (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 dis
tribution of minor gangliosides in the adult rat brain by an immunoflu
orescence 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-Ac-disialoganglios
ide, GD2, GM1b, GM4, IV(3)NeuAc alpha-nLe(4)Cer and IV(6)NeuAc alpha-n
Lc(4)Cer, 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 expre
ssed 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-disi
aloganglioside, which was suggested to be O-Ac-LD1, was detected exclu
sively in both the molecular layer and Purkinje cell layer. The presen
ce of GD2 was restricted to the granular layer. GM4 was associated wit
h some astrocytes, but not with myelin or oligodendrocytes. GM2, GT1a,
GM1b, IV(3)NeuAc alpha-nLc(4)Cer and IV(6)NeuAc alpha-nLc(4)Cer gangl
iosides were not clearly detected in the cerebellar cortex. In other r
egions, such as cerebral cortex, hippocampal formation and spinal cord
, the expression of the gangliosides was also highly localized to a sp
ecific cell type and layer.