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a Cooperative Agricultural Research Center, Prairie View A&M University, Prairie View, Texas 77446
b Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030
c Center for Animal Biotechnology and Genomics, Texas A&M University Health Sciences Center, College Station,Texas 77843
Our objectives were to determine whether specific fucosylated carbohydrate antigens, associated with uterine receptivity in rodents, are expressed in pregnant caprine uterine tissues and polarized uterine luminal epithelial (ULE) cells in culture. Immunofluorescence microscopy on frozen endometrium revealed that expression of the H-type 1 antigen, confined to epithelial cells, was regulated during early pregnancy. Staining was high on Day 5 and low on Days 11 and 13. Strong, uniform apical staining was characteristic of ULE cells between Days 15 and 19 but declined markedly by Day 25. Immunofluorescence analysis of the apical surface of polarized ULE cells cultured in steroid-free medium revealed weak and diffuse staining for the H-type 1 antigen, while progesterone (P4) treatment resulted in the formation of aggregates of punctate staining along the apical surface. Domain-specific biotinylation of polarized ULE cells, coupled with streptavidin precipitation and Western blotting, revealed that six apical surface proteins (31, 33, 42, 55, 60, and 70 kDa) carry the H-type 1 antigen. Therefore, H-type 1 antigen expression is up-regulated in vivo during the periimplantation period, stimulated by P4 on polarized ULE cells in culture, and may be a useful marker for uterine receptivity in this species.
1 Supported by NIH 2S06GM08094 and USDA 97-38814-4157 to G.R.N.
2 Correspondence: G.R. Newton, Prairie View A&M University, P.O. Box 4079, Prairie View, TX 77446-4079. FAX: 409 857 2325; gary_newton{at}pvamu.edu
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