The Expression of p57(kip2) in Mouse Endometrium During Estrus Cycle and Pre- and Peri-implantation Periods.
- Author:
Sung Tae KIM
1
;
Sung Ki LEE
;
Myung Chan GYE
Author Information
1. Department of Obstetrics and Gynecology, Konyang University Hospital, Daejeon, Korea.
- Publication Type:Original Article
- Keywords:
Mouse endometrium;
p57(kip2)
- MeSH:
Animals;
Diestrus;
Endometrium*;
Epithelium;
Estrus*;
Female;
Metestrus;
Mice*;
Phenobarbital;
Proestrus;
Stromal Cells
- From:Korean Journal of Obstetrics and Gynecology
2004;47(7):1342-1347
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: This study was to investigate the localization of CDK inhibitor, p57(kip2) in mouse endometrium during the estrus cycle and pre- and peri-implantation periods. METHODS: The p57(kip2) protein was immunostained from endometrium of mouse sacrificed at diestrus, proestrus, estrus, and metestrus cycle, and at day 1-6 post-coitum (p.c.). RESULTS: The staining in the luminal epithelium was very weak in comparison with glandular and stromal cells. In diestrus stage, immunoreactivity of p57(kip2) was heterogeneously strong in parts of decidualized or degenerated stromal cells. In proestrus stage, strong immunoreactivity p57(kip2) was largely found in stromal cells. But, p57(kip2) was showed low immunoreactivity in estrus stage. In metestrus stage, immunoreactivity of p57(kip2) was heterogeneously strong in decidualized stromal cells. In day 1-2 p.c., immunoreactivity of p57(kip2) was low in some endometrial stromal cells. In day 3-4 p.c., immunoreactivity of p57(kip2) was strong in some endometrial stromal cells. In day 5-6 p.c., immunoreactivity of p57(kip2) was strong in decidual cells. CONCLUSION: These suggest that p57(kip2) may play an essential role in endometrial differentiation for maintenance of implantation, especially decidualization of endometrial stromal cells.
