American Journal of Obstetrics & Gynecology
Volume 194, Issue 3 , Pages 687-693, March 2006

First-trimester trophoblast cell model gene response to hypoxia

  • Nikki Koklanaris, MD

      Affiliations

    • Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine
    • Corresponding Author InformationReprint requests: Nikki Koklanaris, MD, 550 First Ave, NBV-9N27, New York, NY 10016.
  • ,
  • Jerome C. Nwachukwu, BA

      Affiliations

    • Department of Microbiology, New York University School of Medicine, New York, NY
  • ,
  • S. Joseph Huang, MD, PhD

      Affiliations

    • Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT
  • ,
  • Seth Guller, PhD

      Affiliations

    • Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT
  • ,
  • Ksenia Karpisheva, PhD

      Affiliations

    • Department of Microbiology, New York University School of Medicine, New York, NY
  • ,
  • Michael Garabedian, PhD

      Affiliations

    • Department of Microbiology, New York University School of Medicine, New York, NY
  • ,
  • Men-Jean Lee, MD

      Affiliations

    • Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT

Received 8 December 2005; received in revised form 9 January 2006; accepted 17 January 2006.

Objective

Trophoblast invasion, which sets the stage for placentation and pregnancy outcome, likely occurs in a hypoxic environment. We used microarray technology in a trophoblast cell line to identify hypoxia-responsive genes that may impact placentation.

Study design

An immortalized extravillous cytotrophoblast cell line, HTR-8/SVneo, was exposed to normoxia (20% oxygen) or hypoxia (1% oxygen) for 6 hours. Total RNA was harvested and prepared for microarray study. Quantitative reverse transcriptase polymerase chain reaction was performed for array confirmation.

Results

We confirmed the up- and down-regulation of 10 hypoxia-responsive genes using quantitative reverse transcriptase polymerase chain reaction. Ontologic gene categories that were found to be hypoxia-responsive included motility/migration, angiogenesis, and apoptosis.

Conclusion

Specific genes that were found to be up-regulated in this first-trimester array (such as plasminogen activator inhibitor-1 and tissue inhibitor of metalloproteinase 3) have been described in preeclampsia. The hypoxia-responsive genes that we identified may be physiologic in early pregnancy. However, up-regulation of these same genes in later pregnancy augurs poorly.

Key words: Microarray, Trophoblast invasion, Placenta, Hypoxia

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 Presented at the 26th Annual Meeting of the Society for Maternal Fetal Medicine, January 30-February 4, 2006, Miami, FL.

PII: S0002-9378(06)00116-5

doi:10.1016/j.ajog.2006.01.067

American Journal of Obstetrics & Gynecology
Volume 194, Issue 3 , Pages 687-693, March 2006