Biol Reprod
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lee, V. H.
Right arrow Articles by Fields, P. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, V. H.
Right arrow Articles by Fields, P. A.
Agricola
Right arrow Articles by Lee, V. H.
Right arrow Articles by Fields, P. A.

Biology of Reproduction, Vol 52, 868-877, Copyright © 1995 by Society for the Study of Reproduction


ARTICLES

In vitro transformation of rabbit cytotrophoblast cells into syncytiotrophoblast: stimulation of hormone secretion by progesterone and dibutyryl cyclic 3',5'-adenosine monophosphate

VH Lee, SJ Zhang, SM Chang, MJ Fields and PA Fields
Department of Structural and Cellular Biology, University of South Alabama, College of Medicine Mobile 36688, USA.

Rabbit placenta syncytiotrophoblast cells exhibit immunostaining for the hormone relaxin. The objectives of this study were to evaluate the ability of cultured rabbit trophoblast cells to secrete immunoreactive (IR) relaxin and then to study the effects of progesterone, which is essential for maintenance of the placenta and of pregnancy in the rabbit, on that secretion. On Day 1, both treated and untreated trophoblast cell cultures consisted of 90% relaxin-negative mononuclear cells (cytotrophoblast and fibroblast) and 10% relaxin-positive multinuclear cells (syncytiotrophoblast). Media from untreated cultures, collected throughout 9 days of culture, contained low but constant levels of relaxin. Electron microscopy studies indicated that relaxin was localized in dense granules of the multinuclear cells and that these cells formed by fusion of mononuclear cytotrophoblast. Progesterone treatment (40 and 80 ng/ml) increased (p < 0.0001) media concentrations of relaxin, increased the number of desmosomes between cytotrophoblast cells (12 vs. 4 for controls on Day 5), and increased the percentage of multinuclear cells (73% of the cell population vs. 20% for controls on Day 7). Specificity of the progesterone effect was evaluated by treatment of cultures with dibutyryl cAMP (dbcAMP), insulin, hCG, estradiol-17 beta, prostaglandin E2, and prostaglandin F2 alpha. Only dbcAMP (2 mM and 4 mM) produced an increase (p < 0.0001) in media concentrations of relaxin. These results indicate that, like the intact placenta, cultured cytotrophoblast cells fuse to form syncytiotrophoblast and that the latter contain IR relaxin.


This article has been cited by other articles:


Home page
Biol. Reprod.Home page
P. A. Fields, V. H. Lee, A. Jetten, S.-M. T. Chang, and M. J. Fields
B-Chain Sequence and In Situ Hybridization of the Rabbit Placental Relaxin-Like Gene Product
Biol Reprod, August 1, 1999; 61(2): 527 - 532.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
T. Klonisch, S. Hombach-Klonisch, C. Froehlich, J. Kauffold, K. Steger, B.G. Steinetz, and B. Fischer
Canine Preprorelaxin: Nucleic Acid Sequence and Localization within the Canine Placenta
Biol Reprod, March 1, 1999; 60(3): 551 - 557.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1995 by the Society for the Study of Reproduction.