AI Article Synopsis

  • Astrocytic GFAP expression typically rises with age in various brain regions and astrocyte cultures, but this increase is diminished in the presence of microglia.
  • Co-culturing E18 neurons with mixed glia allows GFAP levels to rise, indicating that microglia may influence astrocytic behavior as organisms age.
  • A study analyzing gene expression in mixed glia from young and old rats revealed that age-related gene changes are predominantly independent of neuron presence, with more genes showing increased expression with age than decreased.

Article Abstract

Astrocytic GFAP expression increases during normal aging in many brain regions and in primary astrocyte cultures derived from aging rodent brains. As shown below, we unexpectedly found that the age-related increase of GFAP expression was suppressed in mixed glia (astrocytes+microglia). However, the age-related increase of GFAP was observed when E18 neurons were co-cultured with mixed glia. Thus, the presence of microglia can suppress the age-related increase of GFAP, in primary cultures of astrocytes. To more broadly characterize how aging and co-culture with neurons alters glial gene expression, we profiled gene expression in mixed glia from young (3 mo) and old (24 mo) male rat cerebral cortex by Affymetrix microarray (Rat230 2.0). The majority of age changes were independent of the presence of neurons. Overall, the expression of twofold more genes increased with age than decreased with age. The minority of age changes that were either suppressed or revealed by the presence of neurons may be useful to analyze glial-neuron interaction during aging. Some in vitro changes are shared with those of aging rat hippocampus in studies from the Landfield group (Rowe et al., 2007; Kadish et al., 2009).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703782PMC
http://dx.doi.org/10.1016/j.bbi.2011.12.008DOI Listing

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