Astrocytes participate in central nervous system injury, degenerative
diseases and also perform macrophagic functions. The present work inve
stigates: 1) the effect of the physiological glucocorticoid corticoste
rone (CORT) and the synthetic agonist dexamethasone (DEX) on latex bea
ds phagocytosis by neonatal rat cortical astrocytes in culture, and 2)
tile expression of immunoreactive glucocorticoid receptors (GR) in as
trocytes cultured in different media with or without a pulse applicati
on of CORT. The results indicated that glucocorticoids reduced astrocy
te phagocytic activity, as occurred with macrophages, independently of
the culturing conditions employed. The extent of phagocytosis was inv
ersely related to nuclear immunostaining for GR in cultures in fetal c
alf serum, which contained endogenous glucocorticoid. However, no corr
elation was found between nuclear GR and phagocytosis for cultures in
glucocorticoid-free medium or in medium containing CORT. It is suggest
ed that additional factors, besides the GR, may be involved in glucoco
rticoid modulation of astrocyte phagocytosis.