An early increase in the disialoganglioside GD3 contributes to the development of neuronal apoptosis in culture

D. Melchiorri, F. Martini, E. Lococo, R. Gradini, E. Barletta, Ruggero De Maria Marchiano, A. Caricasole, F. Nicoletti, L. Lenti

Risultato della ricerca: Contributo in rivistaArticolo in rivista

29 Citazioni (Scopus)


We induced apoptosis in primary cultures of cerebellar granule neurons by switching the growing medium into a medium containing lower concentrations of K+(5 or 10 mM instead of 25 mM) or, alternatively, by addition of staurosporine. The apoptotic phenotype was always preceded by an early increase in the intracellular levels of the disialoganglioside GD3, which peaked at 2-6 h and returned back to normal at 12 h. GD3 synthase, the enzyme that forms GD3 from the monosialoganglioside GM3, was also induced at early times after the induction of apoptosis in granule cells. Immunofluorescent staining showed that GD3 increased in neuronal cell bodies and neurites, but was never localized in cell nuclei. In cultures switched into a low K+-containing medium, exogenously applied GD3, but not the disialoganglioside GD1a, accelerated the development of neuronal apoptosis. In contrast, the antisense-induced knock-down of GD3 synthase was protective against granule cell death induced by lowering extracellular K+from 25 to 10 - but not 5 - mM. These results demonstrate that an early and transient increase in GD3 synthesis is one of the factors that contribute to the induction of neuronal apoptosis in culture.
Lingua originaleEnglish
pagine (da-a)609-615
Numero di pagine7
RivistaCell Death and Differentiation
Stato di pubblicazionePubblicato - 2002


  • Animals
  • Apoptosis
  • Cell Biology
  • Cells, Cultured
  • Cerebellar granule neurons
  • Fluorescent Antibody Technique
  • GD3
  • Gangliosides
  • Molecular Biology
  • Neuronal cultures
  • Neurons
  • Rats
  • Rats, Sprague-Dawley


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