ABSTRACT
This article focuses on the potential roles of interferons (IFNs) in establishing
uterine receptivity to implantation. A common feature of the peri-implantation period
of pregnancy in most mammals is production of type I and/or type II IFNs by trophoblasts
that induce and/or stimulate expression of an array of IFN-stimulate genes (ISGs).
These effects range from pregnancy recognition signaling in ruminants through IFN
tau to effects on cellular functions of the uterus and uterine vasculature. For actions
of IFNs, progesterone (P4) is permissive to the expression of many effects and to
the expression of ISGs that are induced directly by an IFN or induced by P4 and stimulated
by an IFN in a temporal and/or cell-specific manner. Uterine receptivity to implantation
is P4 dependent; however, implantation events are preceded by loss of expression of
progesterone (PGR) and estrogen (ESR1) receptors by uterine epithelia. Therefore,
P4 likely acts via PGR-positive stromal cells to induce expression of fibroblast growth
factors-7 and -10 and/or hepatocyte growth factor (progestamedins) that then act via
their respective receptors on uterine epithelia and trophectoderm to affect expression
of ISGs. The permissive effects of P4 on the expression of ISGs and the effects of
P4 to induce and IFNs to stimulate gene expression raise the question of whether uterine
receptivity to implantation requires P4 and IFN to activate unique, but complementary,
cell signaling pathways. Uterine receptivity to implantation, depending on species,
involves changes in the expression of genes for the attachment of trophectoderm to
the uterine lumenal epithelium (LE) and superficial glandular epithelium (sGE), modification
of the phenotype of uterine stromal cells, the silencing of PGR and ESR1 genes, the
suppression of genes for immune recognition, alterations in membrane permeability
to enhance conceptus–maternal exchange of factors, increased vascularity of the endometrium,
activation of genes for transport of nutrients into the uterine lumen, and enhanced
signaling for pregnancy recognition. Differential expression of genes by uterine LE/sGE,
mid- to deep-glandular epithelia (GE), and stromal cells in response to P4 and IFNs
is likely to influence uterine receptivity to implantation in most mammals. Understanding
the roles of IFNs in uterine receptivity for implantation is necessary to develop
approaches to enhance reproductive health and fertility in humans and domestic animals.
KEYWORDS
Interferons - progesterone - pregnancy - interferon-stimulate genes - progestamedins
- fertility - reproductive health
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Fuller W BazerPh.D.
2471 TAMU, Texas A&M University
College Station, TX 77843-2471
Email: fbazer@cvm.tamu.edu