The HLA-G cycle provides for both NK tolerance and immunity at the maternal-fetal interface

Proc Natl Acad Sci U S A. 2015 Oct 27;112(43):13312-7. doi: 10.1073/pnas.1517724112. Epub 2015 Oct 12.

Abstract

The interaction of noncytotoxic decidual natural killer cells (dNK) and extravillous trophoblasts (EVT) at the maternal-fetal interface was studied. Confocal microscopy revealed that many dNK interact with a single large EVT. Filamentous projections from EVT enriched in HLA-G were shown to contact dNK, and may represent the initial stage of synapse formation. As isolated, 2.5% of dNK contained surface HLA-G. However, surface HLA-G-negative dNK contained internalized HLA-G. Activation of dNK resulted in the disappearance of internalized HLA-G in parallel with restoration of cytotoxicity. Surface HLA-G was reacquired by incubation with EVT. This HLA-G cycle of trogocytosis, endocytosis, degradation, and finally reacquisition provides a transient and localized acquisition of new functional properties by dNK upon interaction with EVT. Interruption of the cycle by activation of dNK by cytokines and/or viral products serves to ensure the NK control of virus infection at the interface, and is illustrated here by the response of dNK to human cytomegalo virus (HCMV)-infected decidual stromal cells. Thus, the HLA-G cycle in dNK can provide both for NK tolerance and antiviral immunity.

Keywords: HCMV; cytotoxicity; decidua; human; pregnancy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cytokines / metabolism
  • Cytomegalovirus Infections / immunology*
  • DNA Primers / genetics
  • Female
  • Flow Cytometry
  • HLA-G Antigens / metabolism*
  • Humans
  • Immune Tolerance / immunology*
  • Killer Cells, Natural / immunology*
  • Maternal-Fetal Exchange / immunology*
  • Microscopy, Confocal
  • Pregnancy
  • Real-Time Polymerase Chain Reaction
  • Statistics, Nonparametric
  • Trophoblasts / immunology*

Substances

  • Cytokines
  • DNA Primers
  • HLA-G Antigens