Constraints in antigen presentation severely restrict T cell recognition of the allogeneic fetus
J. Clin. Invest. Adrian Erlebacher, et al. 117:1399 doi:10.1172/JCI28214 [
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Figure 3Act-mOVA expression at the maternal/fetal interface. Sections of implantation sites of Act-mOVA (
A,
C,
E, and
F) or nontransgenic concepti (
B and
D) stained with anti-OVA antibodies (red).
C–
F also show artifactually fluorescent maternal red blood cells (green) to demarcate maternal blood vessels, and DAPI-stained nuclei (blue). (
A and
B) E9.5 implantation sites show high OVA expression in transgenic concepti (
n = 9) confined to trophoblast giant cells (arrowheads) and trophoblasts at the invasive front of the ectoplacental cone (epc; arrow) abutting the maternal decidua (dec). Scale bar: 1 mm. (
C–
E) Higher-power magnifications show that transgenic trophoblasts expressing high levels of OVA had not yet invaded maternal arteries by E9.5 (
C and
D) but were lining maternal vessels (arrows) by E10.5 (
E;
n = 5). Transgenic trophoblasts expressed low levels of OVA in the body of the ectoplacental cone and developing labyrinth (lab), where they also contact maternal blood (compare the purple-tinged color of these structures in
C and
E, reflecting a combination of OVA staining and the DAPI counterstain, with their blue color in
D). Fetal rbc appear blue-tinged due to their nucleation (arrow in
D); the asterisk in
C marks the vestigial uterine lumen. Scale bar: 0.4 mm. (
F) At E13.5, transgenic trophoblasts expressing high levels of OVA were closely associated with or lining (arrowheads) maternal arteries deeper in the decidua (
n = 3). By late gestation, high OVA expression was also apparent in the spongiotrophoblast layer (data not shown). Scale bar: 0.2 mm.