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Possible role of RKIP in cytotrophoblast migration: immunohistochemical and in vitro studies

✍ Scribed by Pasquapina Ciarmela; Daniela Marzioni; Md. Soriful Islam; Peter Clarke Gray; Luigi Terracciano; Teresa Lorenzi; Tullia Todros; Felice Petraglia; Mario Castellucci


Book ID
102313136
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
370 KB
Volume
227
Category
Article
ISSN
0021-9541

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✦ Synopsis


Abstract

Raf kinase inhibitor protein (RKIP) regulates growth and differentiation signaling of mitogen‐activated protein kinases (MAPK), GRK2 and NF‐kappaB pathways each of which regulates cytotrophoblast differentiation and normal placental development. We show here that RKIP is expressed in human normal and preeclampic placentas as detected by immunostaining. RKIP was detected in villous cytotrophoblast in normal placenta and switched to syncytiotrophoblast in pre‐eclampsia (PE)‐complicated pregnancies. RKIP was also localized in extravillous cytotrophoblast of cell islands and cell columns both in normal and in PE placentas, although staining was less uniform in the latter specimens. In order to test RKIP involvement in cytotrophoblast function, we performed in vitro studies on HTR‐8/SVneo cells, a first trimester cytotrophoblast cell line. We show that the RKIP inhibitor locostatin reduces ERK phosphorylation and impairs HTR‐8/SV neo cells motility in wound closure experiments. We also document the presence of GRK2 mRNA, the reduction of phosphorylated RKIP expression by locostatin and the induction of PAI mRNA expression in HTR‐8/SV neo cells, suggesting the involvement of GRK2 and NF‐kappaB pathways in these cells. In conclusion, our work provides evidence that RKIP is a novel factor expressed in cytotrophoblast cells where it likely regulates cell migration. J. Cell. Physiol. 227: 1821–1828, 2012. © 2011 Wiley Periodicals, Inc.


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