Q. Xiao et al., GASTRIN-RELEASING PEPTIDE-LIKE IMMUNOREACTIVITY IS PRESENT IN HUMAN MATERNAL AND FETAL-PLACENTAL MEMBRANES, The Journal of clinical endocrinology and metabolism, 81(10), 1996, pp. 3766-3773
Extracts of human term amnion, placenta, and chorion/decidual tissue (
n = 5) contained gastrin-releasing peptide-like immunoreactivity (GRPL
I) in amounts of 4.7 +/- 2.9 (pmol/g wet wt; mean +/- SEM), 3.6 +/- 1.
1 and 2.9 +/- 1.5, respectively. Using C-terminally directed antisera
and gel filtration chromatography and reverse-phase highperformance li
quid chromatography (HPLC), each tissue contained molecular forms cons
istent with the presence of GRP(1-27) and GRP(18-27) but also containe
d larger amounts of two GRPLI peaks, which apparently are novel GRP-li
ke peptides. In contrast, tissue extracts of human fetal lung containe
d only GRP(1-27), GRP(14-27), and GRP(18-27). Using RT-PCR and specifi
c GRP primers and probes, messenger RNA encoding for GRP was readily d
emonstrable from 6-weeks gestation throughout pregnancy to term in ful
l-thickness membranes, placental villi, and decidua. Positive immunohi
stochemical staining for GRP occurred in extravillous trophoblasts in
decidual septa and fetal membranes, cytotrophoblasts, syncytiotrophobl
ast, and certain stromal cells in placental villi and amniotic epithel
ium. GRPLI and GRP messenger RNA were present from the earliest dates
examined (6-9 weeks) throughout pregnancy to term. Given the proven tr
ophic nature of GRP and related peptides, these peptides may play impo
rtant roles in maternal, placental, and fetal development-during human
pregnancy.