Hl. Chen et al., GESTATION-RELATED EXPRESSION OF THE INTERFERON-GAMMA RECEPTOR GENE INMOUSE UTERINE AND EMBRYONIC HEMATOPOIETIC-CELLS, Journal of leukocyte biology, 55(5), 1994, pp. 617-625
Macrophages and natural killer (NK)-like cells are the major hematopoi
etic cell populations in the cycling and pregnant mouse uterus and are
also found in the embryo. In order to evaluate potential receptivity
of these cells to interferon-gamma (IFN-gamma), tissues taken from cyc
ling and pregnant mice were tested for IFN-gamma receptor (IFN-gamma R
) mRNA and protein. Macrophages were identified immunohistochemically
by using the specific monoclonal antibody F4/80. NK cells were identif
ied by their large size, distinctive intracellular granules, and bindi
ng of a monoclonal antibody to the common leukocyte antigen. In cyclin
g uteri, the abundance of IFN-gamma R mRNA relative to an invariant me
ssage (glyceraldehyde-3-phosphate dehydrogenase) increased during prog
ression of the hormonally regulated estrous cycle. IPN-gamma R mRNA in
situ hybridization signals were slightly higher in macrophage-like th
an in other types of endometrial stromal cells. In pregnant uteri, the
highest proportions of IFN-gamma R mRNB were observed at gestation da
y (g.d.) 16. Specific message and protein were present in uterine macr
ophages by p.d. 7 and in NK cells by g.d. 9. IFN-gamma R expression in
both lineages remained stable through the balance of pregnancy. In em
bryos, IFN-gamma R mRNA increased between g.d. 14 and 16. Specific tra
nscripts were present in many cells at g.d. 14, but none were detected
in embryonic liver macrophages until g.d. 16. The results of this stu
dy; suggest relationships between IFN-gamma R expression and ovarian h
ormones as well as cell maturation and support the postulate that IFN-
gamma receptor-ligand interactions may improve the ability of uterine
and embryonic hematopoietic cells to perform specific tasks during ges
tation.