Journal of Reproductive Immunology
Volume 82, Issue 2 , Pages 119-125, November 2009

Complement production by trophoblast cells at the feto-maternal interface

  • Roberta Bulla

      Affiliations

    • Department of Life Sciences, University of Trieste, 34127 Trieste, Italy
  • ,
  • Fleur Bossi

      Affiliations

    • Department of Life Sciences, University of Trieste, 34127 Trieste, Italy
  • ,
  • Chiara Agostinis

      Affiliations

    • Department of Life Sciences, University of Trieste, 34127 Trieste, Italy
  • ,
  • Oriano Radillo

      Affiliations

    • Laboratory of Clinical Analysis, IRCCS Burlo Garofolo, Trieste, Italy
  • ,
  • Francesca Colombo

      Affiliations

    • Department of Reproductive and Developmental Sciences, IRCCS Burlo Garofolo, University of Trieste, Trieste, Italy
  • ,
  • Francesco De Seta

      Affiliations

    • Department of Reproductive and Developmental Sciences, IRCCS Burlo Garofolo, University of Trieste, Trieste, Italy
    • Global Health, Des Moines University, USA
  • ,
  • Francesco Tedesco

      Affiliations

    • Department of Life Sciences, University of Trieste, 34127 Trieste, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39 040 558 4037; fax: +39 040 558 4023.

Received 23 December 2008; received in revised form 27 May 2009; accepted 5 June 2009. published online 22 July 2009.

Abstract 

An important role played by trophoblast cells at the feto-maternal interface is to exert immunomodulatory functions, including recognition of bacterial and viral agents and recruitment of leucocytes to eradicate pathogens. In this study we present data showing that the trophoblast cell line HTR8/SVneo and freshly isolated human first trimester trophoblast cells (CTBs) synthesize complement molecules C4, C3 and the late complement components, as assessed by ELISA and RT-PCR. Both cell types secrete C4 and C3, and HTR8/SVneo trophoblast cells secrete C6 in a measurable amount. The expression of C4 by HTR8/SVneo trophoblast cells and of C3 and C4 by CTBs was up-regulated by IFNγ, while IL-1α and TNFα had no effect on the expression of complement components. In conclusion, we show that trophoblast cells produce complement components, and that synthesis of these proteins may be regulated by the pro-inflammatory cytokine IFNγ. Complement synthesis by trophoblast cells potentially contributes to placental immune defence from pathogen infection.

Keywords: Complement, Trophoblast cells, Pregnancy, Cytokines

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PII: S0165-0378(09)00253-8

doi:10.1016/j.jri.2009.06.124

Journal of Reproductive Immunology
Volume 82, Issue 2 , Pages 119-125, November 2009