THE PROLACTIN RECEPTOR IN THE FETAL-RAT - CELLULAR-LOCALIZATION OF MESSENGER-RIBONUCLEIC-ACID, IMMUNOREACTIVE PROTEIN, AND LIGAND-BINDING ACTIVITY AND INDUCTION OF EXPRESSION IN LATE-GESTATION
M. Royster et al., THE PROLACTIN RECEPTOR IN THE FETAL-RAT - CELLULAR-LOCALIZATION OF MESSENGER-RIBONUCLEIC-ACID, IMMUNOREACTIVE PROTEIN, AND LIGAND-BINDING ACTIVITY AND INDUCTION OF EXPRESSION IN LATE-GESTATION, Endocrinology, 136(9), 1995, pp. 3892-3900
The cellular distribution and developmental expression of the PRL rece
ptor (PRLR) in the late gestational fetal rat were examined by in situ
hybridization, immunohistochemistry, and radioligand binding. Antisen
se and sense strand RNA probes encoding the long and short isoforms of
the rat PRLR were hybridized to tissue sections under stringent condi
tions. Messenger RNA (mRNA) encoding the two isoforms of the receptor
was expressed widely in tissues derived from all three germ layers; th
ese included various tissues not known previously to contain lactogeni
c receptors, such as the olfactory neuronal epithelium and olfactory b
ulb, trigeminal and dorsal root ganglia, cochlear duct, brown adipose
tissue, submandibular glands, whisker follicles, tooth primordia, and
proliferative and maturing chondrocytes of developing bones. Prominent
expression of PRLR mRNA was also detected in the fetal adrenal cortex
, gastrointestinal and bronchial mucosae, renal tubular epithelia, cho
roid plexus, thymus, liver, pancreas, and epidermis. Immunohistochemic
al studies using monoclonal anti-PRLR antibodies demonstrated that the
distribution of PRLR immunoreactivity was similar to that of PRLR mRN
A, suggesting that the PRLR mRNA is translated to receptor protein in
the fetus in vivo. The encoding of functional PRL receptor proteins by
fetal PRLR mRNA was revealed by the presence of specific rat placenta
l lactogen II-binding sites in fetal adrenal cortex, renal tubules, sm
all intestinal villi, pancreatic ductules and islets, hepatic parenchy
mal cells, choroid plexus ependymal cells, and microsomal fractions of
fetal lung and thymus. Levels of expression of PRLR mRNA and protein
increased between days 17.5 and 20.5 of gestation in a number of fetal
tissues, including the adrenal, pancreas, small intestine, pituitary,
thymus, liver, and submandibular gland. The widespread expression of
the PRLR in the fetal rat and the induction of receptor expression in
late gestation suggest novel roles for the lactogenic hormones in feta
l and neonatal development.