Interferon-tau (IFN-tau) is released by the conceptus and induces two
uterine proteins during early pregnancy: ubiquitin cross-reactive prot
ein (UCRP) and granulocyte chemotactic protein-2 (CCP-P). The present
experiments were designed to determine whether detection (Western blot
) of cytosolic UCRP and release of GCP-2 could be used to examine IFN-
tau signal transduction in cultured endometrial explants and primary e
pithelial cells. Recombinant (r) type 1 IFNs (rboIFN-tau and rboIFN-al
pha; 5, 25, 100 nM) induced UCRP, but only rboIFN-tau induced GCP-2 in
explant culture. Recombinant boIFN-tau and conceptus secretory protei
ns containing native IFN-tau induced UCRP and GCP-2 in cultured primar
y epithelial cells. All concentrations of rboIFN-alpha (25, 50, 100 nM
) induced UCRP, but only the highest concentration induced GCP-2 in cu
ltured primary epithelial cells. Interestingly, phorbol ester (100, 50
0, 1000 ng/ml) induced GCP-2, but it had no effect on UCRP. Because ty
pe 1 IFNs induce UCRP, IFN-tau probably interacts with the janus kinas
e (Jak)-associated IFN-alpha receptor to phosphorylate signal transduc
ers and activators of transcription (STAT) and/or interferon regulator
y factor-1 (IRF-1). However, IFN-tau-specific induction of GCP-2 may i
nvolve a variant type 1 receptor subunit or activators of transcriptio
n that are associated with protein kinase C and the Jak/STAT/IRF-1 pat
hway.