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Departments of Physiology (A.G.U., C.D., C.V.A.) and Legal Medicine (J.M.S.-P.), Faculty of Medicine, University of Santiago de Compostela, 15704 Santiago de Compostela, Spain
Address all correspondence and requests for reprints to: Clara V. Alvarez, University of Santiago de Compostela, Department of Physiology, Faculty of Medicine, Santiago de Compostela, 15704 Spain.
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1) which
binds to GDNF. Thereafter this complex binds to and activates the
tyrosine kinase receptor RET. In this work, for the first time, we have
characterized the expression of both GDNF and RET in the anterior
pituitary. First of all, RT-PCR analysis, Western blot and
immunohistochemistry of the whole anterior pituitary showed that GDNF,
GFR
1 and RET are expressed in this gland. Following
double-immunofluorescence of consecutive sections we found GDNF
immunoreactivity in most cell types, and it was most abundant in
corticotrophs (55%), LH (59%) and FSH-producing cells (81%). In
contrast, while the majority of somatotrophs (87%) were stained for
RET, no positive immunostaining could be detected in other cell types.
Taken together, this data indicate that gonadotrophs and corticotrophs
are the main source of GDNF synthesized in the anterior pituitary and
that the somatotrophs appears to be their target cell. This study
provides direct morphological evidences that GDNF may well be acting in
a paracrine-like fashion in the regulation of somatotroph cell growth
and/or cell function. Received February 4, 2000.
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