Korean J Physiol Pharmacol.
1997 Jun;1(3):285-296.
Effect of glial-neuronal cell co-culture on GFAP expression of
astrocytes
- Affiliations
-
- 1Department of Physiology, Yonsei University, College of Medicine, Seoul 120-752, Korea.
Abstract
-
Injury to brain transforms resting astrocytes to their reactive form,
the hallmark of which is an increase in glial fibrillary acidic protein
(GFAP), the major intermediate filament protein of their cell type. The
overall glial response after brain injury is referred to as reactive
gliosis. Glial-neuronal interaction is important for neuronal
migration, neurite outgrowth and axonal guidance during ontogenic
development. Although much attention has been given to glial regulation
of neuronal development and regeneration, evidences also suggest a
neuronal influence on glial cell differentiation, maturation and
function. The aim of the present study was to analyze the effects of
glial-hippocampal neuronal co-culture on GFAP expression in the
co-cultured astrocytes. The following antibodies were used for double
immunostaining chemistry; mouse monoclonal antibodies for confirm
neuronal cells, rabbit anti GFAP antibodies for confirm astrocytes.
Primary cultured astrocytes showed the typical flat polygonal
morphology in culture and expressed strong GFAP and vimentin.
Co-cultured hippocampal neurons on astrocytes had phase bright cell
body and well branched neurites. About half of co-cultured astrocytes
expressed negative or weak GFAP and vimentin. After 2 hour glutamate
(0.5 mM) exposure of glial-neuronal co-culture, neuronal cells lost
their neurites and most of astrocytes expressed strong GFAP and
vimentin. In Western blot analysis, total GFAP and vimentin contents in
co-cultured astrocytes were lower than those of primary cultured
astrocytes. After glutamate exposure of glial-neuronal co-culture, GFAP
and vimentin contents in astrocytes were increased to the level of
primary cultured astrocytes. These results suggest that neuronal cell
decrease GFAP expression in co-cultured astrocytes and hippocampal
neuronal-glial co-culture can be used as a reactive gliosis model in
vitro for studying GFAP expression of astrocytes.