Placenta
Volume 29, Supplement , Pages 10-16, March 2008

Human Embryonic Stem Cells as Models for Trophoblast Differentiation

  • L.C. Schulz

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
  • ,
  • T. Ezashi

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
  • ,
  • P. Das

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
  • ,
  • S.D. Westfall

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
  • ,
  • K.A. Livingston

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
  • ,
  • R.M. Roberts

      Affiliations

    • Division of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA
    • Division of Biochemistry, University of Missouri-Columbia, Columbia, MO 65211, USA
    • Corresponding Author InformationCorresponding author. Division of Animal Sciences, University of Missouri-Columbia, 240b Bond Life Sciences Center, 1201 E. Rollins Street, Columbia, MO 65211, USA. Tel.: +1 573 882 0908; fax: +1 573 884 9676.

Accepted 24 October 2007. published online 04 December 2007.

Abstract 

Trophectoderm is specified from pluripotent blastomeres at some time prior to blastocyst formation. Proliferating cytotrophoblast derived from trophectoderm is the forerunner of the entire trophoblast component of the mature human placenta, including extravillous cytotrophoblast and syncytiotrophoblast. Recently human embryonic stem cells (hESC) have been employed to study these events in an in vitro situation. Here we review some of the work in this emerging area of trophoblast biology. We concentrate primarily on a model in which colonies of hESC are exposed to BMP4 in stem cell growth medium lacking FGF2. Under both low (4%) and high (20%) O2 conditions, differentiation proceeds unidirectionally towards trophoblast from the outside of the colonies inwards, with the progression fastest under high O2. Immunohistochemical observations performed on whole colonies combined with microarray analysis of mRNA can be employed to track developmental transitions as they occur over time and in two-dimensional space as the cells respond to BMP4.

Keywords: Bone morphogenetic protein-4, Extravillous cytotrophoblast, Human embryonic stem cell, Oxygen, Syncytiotrophoblast

 

PII: S0143-4004(07)00258-5

doi:10.1016/j.placenta.2007.10.009

Placenta
Volume 29, Supplement , Pages 10-16, March 2008