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(American Journal of Pathology. 2006;168:141-150.)
© 2006 American Society for Investigative Pathology

Corticotropin-Releasing Hormone Modulates Human Trophoblast Invasion through Carcinoembryonic Antigen-Related Cell Adhesion Molecule-1 Regulation

Ana-Maria Bamberger*, Vassilis Minas{dagger}, Sophia N. Kalantaridou{ddagger}, Jessica Radde*, Helen Sadeghian*, Thomas Löning*, Ioannis Charalampopoulos§, Jens Brümmer, Christoph Wagener, Christoph M. Bamberger||, Heinrich M. Schulte**, George P. Chrousos{dagger}{dagger} and Antonis Makrigiannakis{dagger}

From the Department of Gynecopathology,* Institute of Pathology, and the Departments of Clinical Chemistry and Internal Medicine,|| University Hospital Eppendorf, Hamburg, Germany; Endokrinologicum Hamburg,** Hamburg, Germany; the Departments of Obstetrics and Gynaecology{dagger} and Pharmacology,§ Laboratory of Human Reproduction, Medical School, University of Crete, Heraklion, Greece; the Department of Obstetrics and Gynaecology,{ddagger} University of Ioannina, Ioannina, Greece; and the First Department of Pediatrics,{dagger}{dagger} Athens University Medical School, Athens, Greece

Abnormalities in the process of trophoblast invasion may result in abnormal placentation. Both the embryonic trophoblast and maternal decidua produce corticotropin-releasing hormone (CRH), which promotes implantation. Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1), which is expressed in extravillous trophoblasts (EVTs) of normal human placenta, may also function in tro-phoblast/endometrial interactions. We investigated whether locally produced CRH plays a role in trophoblast invasion, primarily by regulating CEACAM1 expression. We examined cultures of freshly isolated human EVTs, which express CEACAM1, and an EVT-based hybridoma cell line, which is devoid of endogenous CEACAM1. CRH inhibited EVT invasion in Matrigel invasion assays, and this effect was blocked by the CRH receptor type 1 (CRHR1)-specific antagonist antalarmin. Additionally, CRH decreased CEACAM1 expression in EVTs in a dose-dependent manner. After transfection of the hybridoma cell line with a CEACAM1 expression vector, the invasiveness of these cells was strongly enhanced. This effect was inhibited by addition of blocking monoclonal antibody against CEACAM1. Furthermore, blocking of endogenous CEACAM1 in EVTs inhibited the invasive potential of these cells. Taken together these findings suggest that CRH inhibits trophoblast invasion by decreasing the expression of CEACAM1 through CRHR1, an effect that might be involved in the pathophysiology of clinical conditions, such as preeclampsia and placenta accreta.





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