Platelet-activating factor (PAF) is a phospholipid actively produced b
y human endometrium and deeply involved in the processes of ovoimplant
ation and labor. We recently found that PAF represents a new autocrine
growth factor for a human adenocarcinoma eel line, HEC-1A. Indeed, bi
ologically active PAF is synthesized by HEC-1A cells, under progestero
ne control. In HEC-1A cells, PAF regulates intracellular calcium conce
ntration ([Ca2+]), DNA synthesis and expression of early oncogenes. Al
l these effects are blocked by the receptor antagonist L659,989. Howev
er, while nanomolar concentrations of PAF mobilize [Ca2+], only microm
olar concentrations affect cell growth, suggesting heterogeneity of PA
F receptors or signaling. Two distinct populations of PAF receptors ar
e present in HEC-1A cells, which bind PAF in nanomolar and micromolar
concentrations, respectively. Since HEC-1A cells are producing elevate
d concentrations of PAF and micromolar concentrations of the PAF antag
onist L659,989 inhibit cell proliferation, an autocrine role for PAF i
s suggested in HEC-1A cells.