Activin has been suggested to be an autocrine/paracrine regulator in t
he human placenta. In the present study , we examined the expression o
f the gene encoding activin type II receptor (ActRII) in this tissue.
Using primers corresponding to the published sequence of human ActRII,
a 456bp fragment was obtained from cDNAs prepared from the placenta,
as well as the ovary and brain, by polymerase chain reaction (PCR). So
uthern blot hybridization of the PCR products and DNA cloning and sequ
encing confirmed that the product is the authentic ActRII. Trophoblast
cells prepared from both first trimester and term placentae expressed
the ActRII gene. When trophoblast cells from term placenta were separ
ated into syncytiotrophoblast- and cytotrophoblast-enriched fractions
and incubated for 1-6 days, ActRII gene expression was observed in bot
h cell preparations, with the syncytiotrophoblast-enriched fraction ha
ving higher levels of expression at days 1, 3, and 4. These results pr
ovide the first direct evidence that the activin type II receptor mRNA
is present in human trophoblast cells and strengthen the hypothesis t
hat activin is an autocrine/paracrine regulator of placental function.
To our knowledge, this is also the first report that the ActRII gene
is expressed in the human brain and ovary.