In vitro study on human cytomegalovirus affecting early pregnancy villous EVT's invasion function

Virol J. 2011 Mar 11:8:114. doi: 10.1186/1743-422X-8-114.

Abstract

Background: Human cytomegalovirus (HCMV) is the most common pathogen in uterus during pregnancy, which may lead to some serious results such as miscarriage, stillbirth, cerebellar malformation, fetus developmental retardation, but its pathogenesis has not been fully explained. The hypofunction of extravillous cytotrophoblast (EVT) invasion is the essential pathologic base of some complications of pregnancy. c-erbB-2 is a kind of oncogene protein and closely linked with embryogenesis, tissue repair and regeneration. Matrix metalloproteinase (MMP) is one of the key enzymes which affect EVT migration and invasion function. The expression level changes of c-erbB-2, MMP-2 and MMP-9 can reflect the changes of EVT invasion function.

Results: To explore the influence of HCMV on the invasion function of EVT, we tested the protein expression level changes of c-erbB-2, MMP-2 and MMP-9 in villous explant cultured in vitro infected by HCMV, with the use of immunohistochemistry SP method and western blot. We confirmed that HCMV can reproduce and spread in early pregnancy villus; c-erbB-2 protein mainly expressed in normal early pregnancy villous syncytiotrophoblast (ST) remote plasma membrane and EVT, especially remote EVT cell membrane in villous stem cell column, little expressed in ST proximal end cell membrane and interstitial cells; MMP-2 protein primarily expressed in early pregnancy villous EVT endochylema and rarely in villous trophoblast (VT), ST and interstitial cells; MMP-9 protein largely expressed in early pregnancy villous mesenchyme, EVT and VT endochylema. Compared with control group, the three kinds of protein expression level in early pregnancy villus of virus group significantly decreased (P < 0.05).

Conclusion: HCMV can infect villus in vitro and cause the decrease of early pregnancy villous EVT's invasion function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation*
  • Chorionic Villi / enzymology
  • Chorionic Villi / physiopathology
  • Chorionic Villi / virology*
  • Cytomegalovirus / physiology*
  • Cytomegalovirus Infections / enzymology
  • Cytomegalovirus Infections / genetics
  • Cytomegalovirus Infections / physiopathology
  • Cytomegalovirus Infections / virology*
  • Female
  • Gene Expression Regulation, Developmental
  • Humans
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Pregnancy
  • Pregnancy Complications / enzymology
  • Pregnancy Complications / genetics
  • Pregnancy Complications / physiopathology
  • Pregnancy Complications / virology*
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Trophoblasts / cytology*
  • Trophoblasts / enzymology
  • Trophoblasts / virology*

Substances

  • Receptor, ErbB-2
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9