Placental leucine aminopeptidase/oxytocinase gene regulation by activator protein-2 in BeWo cell model of human trophoblast differentiation

FEBS Lett. 2003 Sep 25;552(2-3):120-4. doi: 10.1016/s0014-5793(03)00897-4.

Abstract

Placental leucine aminopeptidase (P-LAP) is located preferentially in syncytiotrophoblasts in human placenta. Here we investigated P-LAP expression and the regulatory mechanisms in BeWo choriocarcinoma cells with forskolin (FSK)-induced differentiation. Morphologically differentiated cells revealed enhanced P-LAP staining. FSK significantly increased P-LAP activity and mRNA. Deletion or mutation of activator protein-2 (AP-2) binding site in the footprint-3 (-216 to -172) of P-LAP promoter abrogated the stimulatory effects of FSK on luciferase activity of the construct -216/+49. In AP-2-deficient Hep-G2 cells, FSK failed to stimulate luciferase activity of the construct -216/+49. Among the isoforms, BeWo expressed AP-2alpha and AP-2gamma, while FSK increased only AP-2alpha. These results suggest differentiation-dependent P-LAP expression in trophoblasts, which involves increased AP-2alpha binding.

MeSH terms

  • Base Sequence
  • Cell Differentiation
  • Cell Line
  • Colforsin / pharmacology
  • Cystinyl Aminopeptidase / genetics*
  • DNA, Complementary / genetics
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Female
  • Gene Expression Regulation, Enzymologic
  • Humans
  • Immunohistochemistry
  • Luciferases / genetics
  • Models, Biological
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transcription Factor AP-2
  • Transcription Factors / deficiency
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Trophoblasts / cytology*
  • Trophoblasts / metabolism*

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • RNA, Messenger
  • TFAP2A protein, human
  • TFAP2C protein, human
  • Transcription Factor AP-2
  • Transcription Factors
  • Colforsin
  • Luciferases
  • Cystinyl Aminopeptidase
  • leucyl-cystinyl aminopeptidase