Syncytin-1 and glial cells missing a: hypoxia-induced deregulated gene expression along with disordered cell fusion in primary term human trophoblasts

Gynecol Obstet Invest. 2009;68(1):9-18. doi: 10.1159/000209396. Epub 2009 Mar 26.

Abstract

Background/aims: Pre-eclampsia, a major cause of perinatal morbidity, is characterized by alterations in placental oxygen availability and trophoblast differentiation. We investigated how different levels of hypoxia alter the expression of syncytin-1, glial cells missing a (GCMa) and syncytin-1 receptor ASCT2 and affect syncytialization in primary term human trophoblasts.

Methods: Cells were incubated at 1, 3, 6 and 21% O(2) for 24, 48 and 72 h with or without cyclic adenosine monophosphate (cAMP). Gene expression was analyzed by real-time PCR. Syncytialization was assessed using beta-human chorionic gonadotropin measurement and desmoplakin immunostaining.

Results: Following incubation with cAMP at 21% O(2), peak gene expression of syncytin-1 and GCMa was found after 24 h along with syncytium formation at 72 h. Conversely, incubation at 1% O(2) led to a time-dependent reduction of GCMa and syncytin-1 at the transcriptional level. Cell fusion occurred at 21 and 6% O(2) and was suppressed at 1% O(2). ASCT2 mRNA levels were preserved at normoxia and downregulated at 1% O(2) after 48 h.

Conclusion: Our data support the premise that the expression of GCMa and syncytin-1 precedes syncytialization of trophoblasts, e.g. at 6% O(2), which is assumed to resemble physiological conditions. Severe hypoxia is associated with reduced GCMa and syncytin-1 transcripts and altered fusion of primary trophoblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Transport System ASC / metabolism
  • Cell Fusion
  • Cell Hypoxia* / genetics
  • Cell Hypoxia* / physiology
  • DNA-Binding Proteins
  • Down-Regulation
  • Female
  • Gene Expression / genetics*
  • Gene Products, env / metabolism*
  • Humans
  • Minor Histocompatibility Antigens
  • Nuclear Proteins / metabolism
  • Polymerase Chain Reaction
  • Pre-Eclampsia* / genetics
  • Pre-Eclampsia* / metabolism
  • Pregnancy
  • Pregnancy Proteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transcription Factors / metabolism
  • Trophoblasts / metabolism

Substances

  • Amino Acid Transport System ASC
  • DNA-Binding Proteins
  • GCM1 protein, human
  • Gene Products, env
  • Minor Histocompatibility Antigens
  • Nuclear Proteins
  • Pregnancy Proteins
  • RNA, Messenger
  • SLC1A5 protein, human
  • Transcription Factors
  • syncytin