S100B content and secretion decrease in astrocytes cultured in high-glucose medium

Patrícia Nardin, Francine Tramontina, Marina C. Leite, Ana Carolina Tramontina, André Quincozes-Santos, Lucia Maria Vieira de Almeida, Ana Maria Battastini, Carmem Gottfried, Carlos Alberto Gonçalves*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

46 Scopus citations


S100B is an astrocyte calcium-binding protein that plays a regulatory role in the cytoskeleton and cell cycle. Moreover, extracellular S100B, a marker of glial activation in several conditions of brain injury, has a trophic or apoptotic effect on neurons, depending on its concentration. Hyperglycemic rats show changes in glial parameters, including S100B expression. Here, we investigated cell density, morphological and biochemical alterations in primary cortical astrocytes from rats and C6 glioma cells cultured in high-glucose medium. Astrocytes and C6 glioma cells have a reduced content of S100B and glial fibrillary acidic protein when cultured in a high-glucose environment, as well as a reduced content of glutathione and cell proliferation rate. Although these cells have been used indistinctly to study S100B secretion, we observed a contrasting profile of S100B secretion in a high-glucose medium: a decrease in primary astrocytes and an increase in C6 glioma cells. Based on the in vitro neurotrophic effects of the S100B protein, our data suggest that chronic elevated glucose levels affect astrocyte activity, reducing extracellular secretion of S100B and that this, in turn, could affect neuronal activity and survival. Such astrocyte alterations could contribute to cognitive deficit and other impairments observed in diabetic patients.

Original languageEnglish (US)
Pages (from-to)774-782
Number of pages9
JournalNeurochemistry International
Issue number5
StatePublished - Apr 2007


  • Astrocytes
  • Diabetes mellitus
  • GFAP
  • Glutamate uptake
  • Hyperglycemia
  • S100B

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

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