Effect of progesterone on HLA-E gene expression in JEG-3 choriocarcinoma cell line

Am J Reprod Immunol. 2009 Mar;61(3):221-6. doi: 10.1111/j.1600-0897.2008.00684.x.

Abstract

Problem: Among class Ib human leukocyte antigen (HLA) molecules, HLA-E is known to be a major ligand of CD94/NKG2 receptor on natural killer (NK) cells, and to play a pivotal role in recognition of extravillous trophoblasts (EVTs) by maternal immune cells. However, it is scarcely known how HLA-E expression is regulated in EVTs.

Method of study: In this study, we investigated whether progesterone, an essential hormone in maintaining pregnancy, regulated HLA-E expression in EVT-like cell line, JEG-3. HLA-E mRNA amount in cultured JEG-3 cells was assessed by real-time PCR and cell-surface HLA-E protein was analyzed by flowcytometry.

Results: Real-time PCR showed 3.5-fold increase 1 hour after the addition of 1000 ng/ml progesterone. This response was diminished by the addition of RU486, an antagonist for progesterone receptor. Flowcytometry indicated that 1000 ng/ml progesterone slightly enhanced HLA-E expression on the surface of JEG-3.

Conclusion: These results suggest that progesterone up-regulates HLA-E expression in JEG-3 cells through the pathway mediated by progesterone receptor. Our findings might give a new insight into immunomodulatory function of progesterone at fetomaternal interface.

MeSH terms

  • Cell Line, Tumor
  • Choriocarcinoma
  • Gene Expression / drug effects
  • Gene Expression Regulation*
  • HLA Antigens / genetics*
  • HLA-E Antigens
  • Histocompatibility Antigens Class I / genetics*
  • Humans
  • Mifepristone / pharmacology
  • Progesterone / pharmacology
  • Progesterone / physiology*
  • RNA, Messenger / metabolism
  • Receptors, Progesterone / drug effects
  • Receptors, Progesterone / physiology*
  • Trophoblasts / drug effects
  • Trophoblasts / metabolism*
  • Up-Regulation / drug effects

Substances

  • HLA Antigens
  • Histocompatibility Antigens Class I
  • RNA, Messenger
  • Receptors, Progesterone
  • Mifepristone
  • Progesterone