Placenta
Volume 27, Issue 4 , Pages 367-374, April 2006

Bi-potential Behaviour of Cytotrophoblasts in First Trimester Chorionic Villi

  • D. Baczyk

      Affiliations

    • Development and Fetal Health, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Canada
    • These authors contributed equally to the manuscript.
  • ,
  • C. Dunk

      Affiliations

    • Development and Fetal Health, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Canada
    • These authors contributed equally to the manuscript.
  • ,
  • B. Huppertz

      Affiliations

    • Department of Anatomy, University of Technology, Aachen, Germany
  • ,
  • C. Maxwell

      Affiliations

    • Development and Fetal Health, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Canada
    • Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Canada
  • ,
  • F. Reister

      Affiliations

    • Department of obstetrics & Gynecology, University of Ulm, Germany
  • ,
  • D. Giannoulias

      Affiliations

    • Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Canada
  • ,
  • J.C.P. Kingdom

      Affiliations

    • Development and Fetal Health, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Canada
    • Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Canada
    • Corresponding Author InformationCorresponding author. Department of Obstetrics & Gynecology, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario, Canada M5G 1X5. Tel.: +1 416 586 8764; fax: +1 416 586 8565.

Accepted 12 March 2005.

Murine trophoblast stem (TS) cells express fibroblast growth factor receptor 2 (FGFR2) and are maintained in their proliferative state by fibroblast growth factor 4 (FGF4). We show in this report that in the first trimester human placenta FGFR2 expression is similarly found in a subset of villous cytotrophoblast and in proximal anchoring columns. Western analysis demonstrated declining FGFR2 protein expression as gestation advanced, suggesting a similar role for FGF in early human trophoblast proliferation. Mouse TS cell differentiation is known to occur along two distinct transcriptionally-regulated pathways; extravillous trophoblast (EVT) cells invade the uterine wall to promote maternal blood flow whilst syncytiotrophoblast lines chorionic villi in the labyrinth. Similar differentiation steps occur in the human placenta though the fate of human trophoblast stem cells is presently unknown. To investigate the mechanisms underlying human cytotrophoblast differentiation we have developed a novel cultured floating first trimester villous explant model in which denuded first trimester villi spontaneously regenerate syncytiotrophoblast following 48h of culture. Addition of FGF4 and heparin inhibited syncytiotrophoblast regeneration in favor of forming clumps of cytotrophoblast. Proximal cells in these clumps were FGFR2 immuno-reactive and proliferative, intermediate parts expressed α5β1-integrin, while the distal portion expressed HLA-G and the invasive integrin α1β1 indicating differentiation to the EVT phenotype. In contrast, non-denuded villi exposed to FGF4 exhibited similar proliferation of the cytotrophoblast; however, these cells did not express any of the invasive EVT markers. We conclude that FGFR2-positive chorionic cytotrophoblasts exhibit bi-potential behaviour, being capable of forming either syncytiotrophoblast or EVT. We suggest bipotential trophoblast progenitor cells persist during first trimester human placental development.

Keywords: Cytotrophoblast differentiation, Human placental villi, Fibroblast growth factor 4 (FG4), Fibroblast growth factor receptor 2 (FGFR2), Villous explant culture, Syncytial denudation, Syncytiotrophoblast, Extravillous trophoblast

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 Funding: The following supported this research; Physicians Services Inc. Ontario (grant no. 01–44 to JK), Canadian Institutes of Health Research (grant no. 64302 to JK) and Department of Obstetrics & Gynecology, Mount Sinai Hospital (to CM and JK).

PII: S0143-4004(05)00118-9

doi:10.1016/j.placenta.2005.03.006

Placenta
Volume 27, Issue 4 , Pages 367-374, April 2006