Abstract
Since gangliosides are found in high concentration in the CNS1,2 and are topographically localized to the outer surface of neuronal membranes3,4, they have been implicated as receptor molecules. Some hypotheses suggest that gangliosides participate in the regulation of neurogenesis,5synaptogenesis,6 regeneration7 as well as cell-cell interaction.8 Reports that antibody to ganglioside can inhibit neurite outgrowth in vitro9,10 and can interfere with synaptogenesis and neurogenesis in vivo indirectly support these hypotheses.
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J. A. Skrivanek, R. W. Ledeen, R. U. Margolis, and R. K. Margolis, Gangliosides associated with microsomal subfractions of brain: Comparison with synaptic plasma membranes, J, Neurobiol. 13:95 (1982).
P. Fishman and R. Brady, Biosynthesis and function of ganglio-sides, Science 194:904 (1976).
S. P. Mahadik, B. Hungund, and M. M. Rapport, Topographic studies of glycoproteins of intact synaptosomes from rat brain cortex, Biochimica & Biophys. Acta 515:240 (1978).
B. Hungund and S. P. Mahadik, Topographic studies of ganglio-sides of intact synaptosomes from rat brain cortex, Neurochem. Res. 6:183 (1981).
M. Willinger and M. Schachner, GM1 ganglioside as marker for neuronal differentiation in mouse cerebellum, Dev. Biol. 74:101 (1980).
K. Obata, M. Oide, and S. Handa, Effects of glycolipids on in vitro development of neuromuscular junction, Nature 266:369 (1977).
A. Gorio, P. Marini, and R. Zanoni, Muscle reinnervation — III. Motoneuron sprouting capacity, enhancement by exogenous gangliosides, Neurosci. 3:417 (1983).
T. Yamakawa and Y. Nagai, Glycolipids at the cell surface and their biological function, TIBS 3:128 (1979).
M. Schwartz and N. Spirman, Sprouting from chicken embryo dorsal root ganglia induced by nerve growth factor is specifically inhibited by affinity-purified antiganglioside antibodies, Proc. Natl. Acad. Sci. USA 79:6080 (1982).
N. Spirman, B. Sela, and M. Schwartz, Antiganglioside antibodies inhibit neuritic outgrowth from regenerating goldfish retinal explants, J. Neurochem. 39:874 (1982).
E. Kasarskis, S. Karpiak, M.M. Rapport, R. Yu, N. Bass, Abnormal maturation of cerebral cortex and behavior in adult rats after neonatal administration of antibodies to GMl ganglioside, Dev. Brain Res. 1:1 (1980).
F. J. Roisen, H. Bartfeld, R. Nagele, and G. Yorke, Ganglioside stimulation of axonal sprouting in vitro, Science 214:577 (1981).
A. Leon, L. Facci, D. Benvegnu, and G. Toffano, Morphological and biochemical effects of gangliosides in neuroblastoma cells, Dev. Neurosci. 5:108 (1982).
A. Gorio, P. Marini, and R. Zanoni, Muscle reinnervation — III. Motoneuron sprouting capaticy, enhancement by exogenous gangliosides, Neurosci. 3:417 (1983).
D. Kleinebeckel, Acceleration of muscle re-innervation in rats by ganglioside treatment: An electromyographic study, Eur. J. Pharm. 80:243 (1982).
G. Tettamanti, B. Veerando, S. Roberti, V. Chigorno, S. S. Sonnino, R. Ghidoni, P. Orlando, and P. Masari, The fate of exogenously administered brain gangliosides. In “Gangliosides in Neurological and Neuromuscular Function, Development and Repair”, M. Rapport and A. Gorio, eds., Raven Press, New York, pp. 225–240 (1981).
G. Toffano, D. Benvegnu, A. Bonetti, L. Facci, A. Leon, P. Orlando, R. Ghidoni, and G. Tettamanti, Interaction of GM1 ganglioside with crude brain neuronal membranes, J. Neurochem. 35:861 (1980).
P. Fishman, J. Moss, and V. Manganiello, Synthesis and uptake of gangliosides by choleragen-responsive human fibroblasts, J. Biochem. 16:1871 (1977).
E. O’Keefe and P. Cuatrecasas, Persistence of exogenous, inserted ganglioside GM1 on the cell surface of cultured cells, Life Sci. 21:1649 (1977).
S. Kanda, K. Inoue, S. Nojima, H. Utsumi, and H. Wiegandt, Incorporation of spin-labeled ganglioside analogues into cell and liposomal membranes, J. Biochem. 91:1707 (1982).
O. Steward, C. Cotman, and G. Lynch, A quantitative autoradiographic and electrophysiological study of the reinnervation of the dentate gyrus by the contralateral entorhinal cortex following ipsilateral entorhinal lesions, Brain Res. 114:181 (1976).
O. Steward, Assessing the functional significance of lesion-induced neuronal plasticity, Int. Rev. Neurobiol. 23:197 (1982).
A. Caceres and O. Steward, Dendritic reorganization in the denervated dentate gyrus of the rat following entorhinal cortical lesions: a golgi and electron microscopic analysis, J. Comp. Neurol. 214:387 (1983).
J. Loesche and O. Steward, Behavioral correlates of denervation and reinnervation of the hippocampal formation of the rat: Recovery of alternation performance following unilateral entorhinal cortex lesions, Brain Res. 2:31 (1977).
O. Steward, Reinnervation of dentate gyrus by homologous afferents following entorhinal cortical lesions in adult rats, Science 194:426 (1976).
O. Steward and S. Vinsant, Collateral projections of cells in the surviving entorhinal area which reinnervate the dentate gyrus of the rat following unilateral entorhinal lesions, Brain Res. 149:216 (1978).
O. Steward and S. Scoville, Cells of origin of entorhinal cortical afferents to the hippocampus and fascia dentata of the rat, J. Comp. Neurol. 169:347 (1976).
O. Steward and S. Vinsant, Identification of the cells of origin of a central pathway which sprouts following lesions in mature rats, Brain Res. 147:223 (1978).
S. Karpiak, M. M. Rapport, and F. Bowen, Immunologically induced behavioral and electrophysiological changes in the rat, Neuropsychologia 12:313 (1973).
S. Karpiak, Ganglioside treatment improves recovery of altena-tion behavior after unilateral entorhinal cortex lesion, Exp. Neurol. 81:330 (1983).
E. Bremer and L. Hakomori, GM3 ganglioside induces hamster fibroblast growth inhibition in chemically-defined medium: Ganglioside may regulate growth factor receptor function, Biochem. Bioph. Res, Comm. 106:711 (1982).
L. Irwin, D. Michael, and C. Irwin, Ganglioside patterns of fetal rat and mouse brain, J. of Neurochem. 34:1527 (1980).
F. Cumar, B. Maggio, and R. Capputo, Dopamine release from nerve endings induced by polysialogangliosides, Biochem. and Biophys. Res. Comm. 84:65 (1978).
D. Purpura and H. Baker, Neurite induction in mature cortical neurones in feline GM1-ganglioside storage disease, Nature 266:553 (1977).
S. Karpiak, F. Vilim, and S. Mahadik, GM1 ganglioside facilitates functional recovery after an entorhinal lesion; increase in AChE in dentate gyrus, Soc. Neurosci Abstr. 9:699 (1983).
B. Oderfeld-Nowak, M. Jezierska, J. Ulas, K. Mitros, and A. Wieraszko, Plastic responses of cholinergic parameters in the hippocampus induced by entorhinal cortex lesions are intensified by GM1 ganglioside treatment, Abstr from the Cell Biology of Neuronal Plasticity, Sardinia, Italy, p. 115 (1983)
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© 1984 Plenum Press, New York
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Karpiak, S.E. (1984). Exogenous Gangliosides Enhance Recovery from CNS Injury. In: Ledeen, R.W., Yu, R.K., Rapport, M.M., Suzuki, K. (eds) Ganglioside Structure, Function, and Biomedical Potential. Advances in Experimental Medicine and Biology, vol 174. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1200-0_41
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DOI: https://doi.org/10.1007/978-1-4684-1200-0_41
Publisher Name: Springer, Boston, MA
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