ANALYSIS OF MESSENGER-RIBONUCLEIC-ACID AND PROTEIN FOR THE LIGANDS AND RECEPTORS OF THE PLATELET-DERIVED GROWTH-FACTOR SIGNALING PATHWAY INTHE PLACENTA, EXTRAEMBRYONIC MEMBRANES, AND UTERUS DURING THE LATTER HALF OF MURINE GESTATION
Mc. Bidwell et al., ANALYSIS OF MESSENGER-RIBONUCLEIC-ACID AND PROTEIN FOR THE LIGANDS AND RECEPTORS OF THE PLATELET-DERIVED GROWTH-FACTOR SIGNALING PATHWAY INTHE PLACENTA, EXTRAEMBRYONIC MEMBRANES, AND UTERUS DURING THE LATTER HALF OF MURINE GESTATION, Endocrinology, 136(11), 1995, pp. 5189-5201
Previous investigation of ligand and receptor messenger RNA (mRNA) exp
ression implicated the platelet-derived growth factor (PDGF) pathway a
s a participant in the maintenance of pregnancy and fetal development
during the first half of murine gestation. We extended these studies u
sing Northern and in situ RNA hybridization and immunohistochemical de
tection of protein to evaluate the expression kinetics and cell-specif
ic localization of PDGF-A, PDGF-B, PDGF alpha-receptor, and PDGF beta-
receptor in mouse placenta, extraembryonic membranes, and uterus durin
g the second half of gestation (days 9.5-18.5). Northern blotting expe
riments reveal that mRNAs for the PDGF signaling components exhibit un
ique time-dependent and tissue-specific expression in the placenta and
uterus, being progressively and coordinately up-regulated as gestatio
n proceeds. Cell-specific localization of mRNA and protein by in situ
hybridization and immunohistochemistry demonstrates widespread express
ion in multiple cell types of the placenta, gravid uterus, and extraem
bryonic membranes. Abundant PDGF protein and mRNA expression is exhibi
ted in the nucleated fetal erythroid progenitor cells that originate i
n the extraembryonic membranes and circulate throughout the developing
conceptus. Our data together with those of previous studies demonstra
te that PDGF ligands and receptors are globally expressed in many cell
types within fetal and maternal tissues during murine gestation and,
thus, imply a potential role for PDGF in fetal development and materna
l-fetal interactions.