Skip to main content
Log in

Developmental profiles of gangliosides in mouse and rat cerebral cortex

  • Rapid Communication
  • Published:
Wilhelm Roux's archives of developmental biology Aims and scope Submit manuscript

Summary

Developmental profiles of 11 gangliosides, concentration of lipid- and glycoprotein-bound sialic acid, and activity of AChE of the rat and mouse cerebral cortex were followed from the 7th day of gestation to the 21st postnatal day.

There are three main changes in ganglioside concentration, which are similar in both species. The first occurs from gestation day 10 until birth: parallel to decreased proliferation, cell migration, and neuroblast differentiation, GM3 and GD3 in mouse cortex and GD3 in the rat's decreases in favor of GQ1b, GT1b, and GD1a.

The second occurs from birth until the first postnatal week: Parallel to increased growth and arborization of dendrites and axons as well as synaptogenesis in rats and mice, there is a two-fold rise of GD1a, whereas GQ1b and GT1b remain on a nearly constant level. Concomitantly, GM3 and GD3 decreases. The third period of ganglioside changes starts in the second postnatal week, parallel to onset of myelination, and is characterized by an increase of GM1 in parallel with a decrease of the polysialogangliosides GT1b and GQ1b.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Altman J (1967) Postnatal growth and differentiation of the mammalian brain with implications for a morphological theory of memory. In: Quarton G, Melnechuk T, Schmitt OF (eds) The neurosciences: a study program. Rockefeller University Press, New York, pp 723–743

    Google Scholar 

  • Ando S, Chang H, Yu RK (1978) High-performance thin-layer chromatography and densitometric determination of brain ganglioside composition of several species. Anal Biochem 89:437–450

    PubMed  Google Scholar 

  • Berra B, Cestaro BO, Salé F, Venerando B, Beltrame D, Cantone A (1978) Gangliosides and neuraminidases in foetal rat brain. Bull Mol Biol Med 3:86–97

    Google Scholar 

  • Breer H, Rahmann H (1977) Cholinesteraseaktivität und Hirnganglioside während der Fischentwicklung. Wilhelm Roux's Arch 171:65–72

    Google Scholar 

  • Cochran IR, Yu RK, Ledeen RW (1981) Myelin ganglioside: an unusual pattern in the avian central nervous system. J Neurochem 36:696–702

    PubMed  Google Scholar 

  • Dreyfus H, Louis JC, Harth S, Pettmann B, Urban PF, Mandel P (1979) Development of gangliosides and sialyltransferase activities during maturation of isolated neurons. Proc 5th Int Symp on Glycoconjugates, Kiel, p 704

  • Dreyfus H, Urban PF, Edel-Hath S, Mandel P (1975) Developmental patterns of gangliosides and of phospholipids in chick retina and brain. J Neurochem 25:245–250

    PubMed  Google Scholar 

  • Ellman GL, Courtney KD, Andres VJ, Featherstone RM (1961) A new rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 7:88–95

    Article  PubMed  Google Scholar 

  • Irwin LN, Chen H, Barraco RA (1976) Ganglioside, protein, hexose, and sialic acid changes in the trisected optic tectum of the chick embryo. Dev Biol 49:29–39

    PubMed  Google Scholar 

  • Irwin LN, Irwin CC (1979) Developmental changes in ganglioside composition of Hippocampus, retina and optic tectum. Dev Neurosci 2:129–135

    Google Scholar 

  • Irwin LN, Michael DB, Irwin CC (1980) Ganglioside pattern of fetal rat and mouse brain. J Neurochem 34:(6), 1527–1530

    PubMed  Google Scholar 

  • Jourdian GW, Den C, Roseman S (1971) The sialic acids: XI. A. periodate-resorcinol method for the quantitative estimation of free sialic acids and their glycosides. J Biol Chem 246:430–435

    PubMed  Google Scholar 

  • Lowry OH, Rosebrough NJ, Far AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275

    PubMed  Google Scholar 

  • Martin R (1962) Entwicklungszeiten des ZNS von Nagern mit Nesthocker- und Nestflüchterontogenese (Cavia cobaya Schreb. und Rattus norvegicus Erxleben). Rev Suisse Zool 69:617–727

    Google Scholar 

  • Merat A, Dickerson JWT (1973) The effect of development on the gangliosides of rat and pig brain. J Neurochem 20:873–880

    PubMed  Google Scholar 

  • Miettinen T, Takki-Lukkainen IT (1959) Use of butyl acetate in determination of sialic acid. Acta Chem Scand 13:856–858

    Google Scholar 

  • Peters VB, Flexner LB (1950) Biochemical and physiological differentiation during morphogenesis. VII. Quantitative morphological studies on the developing cerebral cortex of the fetal guinea pig. Am J Anat 86:133–161

    PubMed  Google Scholar 

  • Rösner H (1975) Changes in the content of gangliosides and glycoproteins and in the ganglioside pattern of the chicken brain. J Neurochem 24:815–816

    PubMed  Google Scholar 

  • Rösner H (1977) Gangliosides, sialoglycoproteins and acetylcholinesterase of the developing mouse brain. Wilhelm Roux's Arch Dev Biol 183:325–335

    Google Scholar 

  • Rösner H (1980) Ganglioside changes in the chicken optic lobes and cerebrum during embryonic development. Wilhelm Roux's Arch Dev Biol 188:206–213

    Google Scholar 

  • Rösner H (1981) Isolation and preliminary characterisation of novel polysialogangliosides from embryonic chicken brain. J Neurochem 37:993–997

    PubMed  Google Scholar 

  • Rösner H (1982) Ganglioside changes in the chicken optic lobes as biochemical indicators of brain development and maturation. Brain Res 236:49–61

    PubMed  Google Scholar 

  • Rösner H, Segler K, Rahmann H (1979) Changes of brain gangliosides in chicken and mice during heterothermic development. J Therm Biol 4:121–124

    Google Scholar 

  • Sonnino S, Ghidoni R, Masserini M, Aporti F, Tettamanti G (1981) Changes in rabbit brain cytosolic and membrane-bound gangliosides during prenatal life. J Neurochem 36:227–232

    PubMed  Google Scholar 

  • Sugita N (1918) Comparative studies on the growth of the cerebral cortex. J Comp Neurol 29:119–162

    Google Scholar 

  • Suzuki K (1965) The pattern of mammalian brain gangliosides III; regional and developmental differences. J Neurochem 12:969–979

    PubMed  Google Scholar 

  • Suzuki K (1967) Formation and turnover of the major brain gangliosides during development. J Neurochem 14:917–925

    PubMed  Google Scholar 

  • Svennerholm L (1957) Quantitative estimation of sialic acids. Biochim Biophys Acta 24:604–611

    PubMed  Google Scholar 

  • Svennerholm L (1963) Chromatographic separation of human brain gangliosides. J Neurochem 10:613–623

    PubMed  Google Scholar 

  • Tettamanti G, Bonali F, Marcesini S, Zambotti V (1973) A new procedure for the extraction, purification and fractionation of brain gangliosides. Biochim Biophys Acta 296:160–170

    PubMed  Google Scholar 

  • Vanier MT, Holm M, Öhmann R, Svennerholm L (1971) Developmental profiles of gangliosides in human and rat brain. J Neurochem 18:581–592

    PubMed  Google Scholar 

  • Yu RK, Ando S (1980) Structures of some new complex gangliosides of fish brain. Adv Exp Med Biol 125:33–45

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hilbig, R., Rösner, H., Merz, G. et al. Developmental profiles of gangliosides in mouse and rat cerebral cortex. Wilhelm Roux' Archiv 191, 281–284 (1982). https://doi.org/10.1007/BF00848417

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00848417

Key words

Navigation