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Tissue transglutaminase expression and activity in placenta.

Nicola J Robinson1, Jocelyn D Glazier, Susan L Greenwood

  • 1Academic Unit of Obstetrics and Gynaecology, Maternal and Fetal Research Centre, University of Manchester, St Mary's Hospital, Hathersage Road, Manchester M13 0JH, UK.

Placenta
|December 13, 2005
PubMed
Summary

Tissue transglutaminase (tTG) is present in the human placenta, with higher expression later in pregnancy. This enzyme, a coeliac disease autoantigen, may be targeted by maternal antibodies at the placental microvillous membrane.

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Area of Science:

  • Reproductive biology
  • Immunology
  • Enzymology

Background:

  • Tissue transglutaminase (tTG) is a key autoantigen in coeliac disease.
  • Coeliac disease is associated with adverse pregnancy outcomes.
  • The role of tTG in placental function and pregnancy is not fully understood.

Purpose of the Study:

  • To investigate the expression, distribution, and activity of tTG in the human placenta.
  • To determine if placental tTG is a potential target for maternal autoantibodies.

Main Methods:

  • Immunochemical techniques (e.g., Western blotting, immunohistochemistry) were used to detect tTG protein.
  • Reverse transcription-polymerase chain reaction (RT-PCR) was employed to assess tTG mRNA levels.
  • Primary cell cultures (trophoblast, fibroblasts, decidual stromal cells) were utilized for confirmation.

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  • Enzymatic activity was measured using substrate incorporation assays.
  • Main Results:

    • tTG protein and mRNA were detected in placental stromal cells and trophoblast throughout pregnancy, with increased levels in later stages.
    • Decidual cells were also identified as a source of tTG.
    • tTG activity was associated with the fibroblast extracellular matrix and the syncytial microvillous membrane (MVM).
    • Several tTG target polypeptides were identified on the MVM.

    Conclusions:

    • tTG is expressed and active in the human placenta, particularly in the MVM.
    • Placental tTG represents a potential target for maternal autoantibodies, which could contribute to adverse pregnancy outcomes in conditions like coeliac disease.