Pleiotrophin Messenger Ribonucleic Acid Levels Increase in Mouse Endometrial Stromal Cells During Decidualization
In mice (and other species) fibroblast-like endometrial stromal cells differentiate into large decidual cells during early pregnancy. These decidual cells, which play an important function during the process of embryo implantation, eventually die or form the maternal component of the placenta. In th...
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Veröffentlicht in: | Endocrinology (Philadelphia) 2001-02, Vol.142 (2), p.955-958 |
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Zusammenfassung: | In mice (and other species) fibroblast-like endometrial stromal cells
differentiate into large decidual cells during early pregnancy. These
decidual cells, which play an important function during the process of
embryo implantation, eventually die or form the maternal component of
the placenta. In the current study, with the use of subtractive
hybridization methods and Northern blot analysis, we found that
steady-state pleiotrophin transcript levels are increased in uterine
horns undergoing artificially induced decidualization compared to
control horns. Steady-state pleiotrophin transcript levels were
significantly (P < 0.01) greater in uterine horns
undergoing decidualization compared to the control horn at 48 h and 72
h, but not 24 h, after the application of the deciduogenic stimulus to
appropriately sensitized uteri. This increase in pleiotrophin
transcript levels was localized to the endometrial stromal cells
undergoing decidualization, as determined by in situhybridization. Finally, we also determined if pleiotrophin
transcript levels were greater in implantation segments compared to
inter-implantation segments of the uterus during early pregnancy.
Steady-state pleiotrophin transcript levels were significantly
(P < 0.01) greater in implantation compared to
inter-implantation segments on day 6 to 8, but not 5 (day 1 = vaginal
plug), of pregnancy. In conclusion, pleiotrophin transcript levels
increase in the endometrial stromal cells during decidualization
suggesting that it might play a role in the process. |
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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.142.2.8111 |