Sa. Sands et Bm. Chronwall, GFAP EXPRESSION INDUCED BY DOPAMINE D-2 RECEPTOR AGONISTS IN THE RAT PITUITARY INTERMEDIATE LOBE, Endocrine, 4(1), 1996, pp. 35-42
This study was conducted to determine if intermediate lobe glial-like
cells are affected by compounds that regulate melanotrope biosynthetic
activity via the dopamine D-2 receptor, Glial-like cells were stellat
e, and expressed glial fibrillary acidic protein (GFAP) and vimentin i
n cell bodies and processes as revealed by immunohistochemistry. Follo
wing bromocriptine and quinpirole treatments, the number of cell bodie
s and processes expressing vimentin did not change, whereas those expr
essing GFAP increased, although never to exceed the number of vimentin
containing structures, The percent of cells and processes coexpressin
g GFAP and vimentin also increased. The GFAP response was reversible b
y haloperidol treatment following the agonist treatment, Haloperidol t
reatment alone did not change GFAP expression. Thus, following D-2 rec
eptor agonist treatment, GFAP was induced in pre-existing vimentin-pos
itive glial cells, Dopamine D-2 receptor mRNA and protein were detecte
d in melanotropes, but not in cells expressing GFAP or vimentin. Altho
ugh glial-like cells may express dopamine D-2 receptor mRNA and protei
n below the detection levels of our methods, the possibility of an ind
irect effect via dopamine D-2 receptor agonists acting on melanotropes
needs to be considered.