Peripheral mononuclear cells (MNC) in culture release a biologically a
ctive hCG. This effect is detectable during pregnancy with a maximum b
etween the 9th and 16th wk. Peripheral MNC already secrete hCG between
the 7th and 11th d after embryo transfer. The secretion of hCG is act
ivated by the PKC-activator TPA. TPA induces hCG release into the medi
um, thus causing a decrease in intracellular hCG content. In contrast,
db-cAMP inhibites hCG secretion into the medium. Protein synthesis in
hibitors of transcription and translation suppress the production and
secretion of hCG. Peripheral natural killer (NK) cells (CD 56+/CD16+)
and monocytes (CD14+) show the highest secretion rates. IL-1 beta, IL-
4, IL-6, IL-10, TNF alpha, and GM-CSF stimulate, whereas IL-2 and INF
gamma inhibit, the hCG secretion of mononuclear cells. Flow cytometric
experiments with hCG antibody demonstrate a binding of hCG on the sur
face of monocytes more than lymphocytes. The binding capacity is impro
ved during pregnancy. Different hCG bands are shown in the Western blo
t analysis. We could confirm the mRNA of beta hCG and alpha CG are in
MNC as well in the placental control. Peripheral MNC, first and foremo
st NK cells and monocytes, produce and secrete hCG during pregnancy, w
hich play an important role for the corpus luteum rescue during the ea
rly gestational age and possibly for the immunotolerance. (C) Elsevier
Science Inc. 1998