Previously, we showed that erythropoietin (Epo) is produced in the mouse ut
erus, where Epo is indispensable for estrogen (E-2)-dependent angiogenesis.
Expression of uterine Epo mRNA is stimulated by E-2 and hypoxia. The hypox
ic induction requires the presence of E-2. In the present study, we examine
d other female reproductive organs in the mouse with respect to Epo mRNA ex
pression and its stimuli (E-2 and hypoxia)-induced changes. Although Epo mR
NA expression was seen in the ovary and oviduct, the E-2-induced stimulatio
n of Epo mRNA was found only in the oviduct. The E-2-induced stimulation in
the oviduct was transient and rapidly downregulated. Epo mRNA expression i
n the oviduct was hypoxia inducible, in both the presence and the absence o
f E-2. E-2-dependent production of Epo and its mRNA expression were also fo
und by use of cultured oviducts. The E-2 action is probably mediated throug
h the E-2 receptor, and de novo protein synthesis is not required for E-2 i
nduction of Epo mRNA. In the oviduct, the ampulla and isthmus regions produ
ce Epo.