The expression of a novel natural killer inhibitory molecule, Cho-1, on the chorionic cytotrophoblast cells of successful pregnancy, but not of spontaneous abortion

Pathol Int. 2000 Oct;50(10):824-31. doi: 10.1046/j.1440-1827.2000.01115.x.

Abstract

The regulatory mechanism of the recognition and cytotoxicity by natural killer (NK) cells in placental tissue remains unclarified. Previous reports indicated that monoclonal antibody Cho-1-defined molecule (Cho-1 molecule) may act as the negative regulator in the cytotoxicity by human NK cells. The Cho-1 molecule is composed of non-covalently associated cell surface molecules of approximately 200 kDa and 40 kDa. In the present study we analyzed the expression of this novel molecule in extravillous cytotrophoblast cells, which are presumed to be exposed to the cytotoxic action by maternal NK cells, from clinical cases of successful pregnancy and spontaneous abortion. By using monoclonal antibody Cho-1, our immunohistochemical data indicated that the Cho-1 molecule is clearly expressed in the cytotrophoblast cells of the early phase of successful pregnancy, but only weakly expressed in those from spontaneous abortion. The cytotrophoblast cells in the late phase (9-10 months) of pregnancy also expressed this molecule. Fluorescence-activated cell sorter analysis also showed that it is expressed on the cytotrophoblast cell surface of successful pregnancy but not on that of spontaneous abortion, suggesting that Cho-1 antigen may act as a negative regulator of the cytotoxicity by NK cells in successful pregnancy of the fetus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortion, Spontaneous
  • Adult
  • Antibodies, Monoclonal
  • Antigens, Surface / metabolism
  • Chorion / cytology
  • Chorion / immunology
  • Chorion / metabolism*
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism*
  • Microtubule-Associated Proteins / metabolism*
  • Pregnancy / immunology
  • Pregnancy / metabolism*
  • Pregnancy Trimester, First
  • Receptors, Immunologic / immunology
  • Receptors, Immunologic / metabolism*
  • Receptors, KIR
  • Trophoblasts / cytology
  • Trophoblasts / immunology
  • Trophoblasts / metabolism*

Substances

  • Antibodies, Monoclonal
  • Antigens, Surface
  • KIF23 protein, human
  • Microtubule-Associated Proteins
  • Receptors, Immunologic
  • Receptors, KIR