TY - JOUR
T1 - Mice Expressing Only Monosialoganglioside GM3 Exhibit Lethal Audiogenic Seizures
AU - Kawai, Hiromichi
AU - Allende, Maria Laura
AU - Wada, Ryuichi
AU - Kono, Mari
AU - Sango, Kazunori
AU - Deng, Chuxia
AU - Miyakawa, Tsuyoshi
AU - Crawley, Jacqueline N.
AU - Werth, Norbert
AU - Bierfreund, Uwe
AU - Sandhoff, Konrad
AU - Proia, Richard L.
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2001/3/9
Y1 - 2001/3/9
N2 - Gangliosides are a family of glycosphingolipids that contain sialic acid. Although they are abundant on neuronal cell membranes, their precise functions and importance in the central nervous system (CNS) remain largely undefined. We have disrupted the gene encoding GD3 synthase (GD3S), a sialyltransferase expressed in the CNS that is responsible for the synthesis of b-series gangliosides. GD3S-/- mice, even with an absence of b-series gangliosides, appear to undergo normal development and have a normal life span. To further restrict the expression of gangliosides, the GD3S mutant mice were crossbred with mice carrying a disrupted GalNAcT gene encoding β 1,4-N-acetylgalactosaminyltransferase. These double mutant mice expressed GM3 as their major ganglioside. In contrast to the single mutant mice, the double mutants displayed a sudden death phenotype and were extremely susceptible to induction of lethal seizures by sound stimulus. These results demonstrate unequivocally that gangliosides play an essential role in the proper functioning of the CNS.
AB - Gangliosides are a family of glycosphingolipids that contain sialic acid. Although they are abundant on neuronal cell membranes, their precise functions and importance in the central nervous system (CNS) remain largely undefined. We have disrupted the gene encoding GD3 synthase (GD3S), a sialyltransferase expressed in the CNS that is responsible for the synthesis of b-series gangliosides. GD3S-/- mice, even with an absence of b-series gangliosides, appear to undergo normal development and have a normal life span. To further restrict the expression of gangliosides, the GD3S mutant mice were crossbred with mice carrying a disrupted GalNAcT gene encoding β 1,4-N-acetylgalactosaminyltransferase. These double mutant mice expressed GM3 as their major ganglioside. In contrast to the single mutant mice, the double mutants displayed a sudden death phenotype and were extremely susceptible to induction of lethal seizures by sound stimulus. These results demonstrate unequivocally that gangliosides play an essential role in the proper functioning of the CNS.
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U2 - 10.1074/jbc.C000847200
DO - 10.1074/jbc.C000847200
M3 - Article
C2 - 11133999
AN - SCOPUS:0035831502
SN - 0021-9258
VL - 276
SP - 6885
EP - 6888
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 10
ER -