Characterization of the expression of MHC proteins in human embryonic stem cells

  1. Micha Drukker*,,
  2. Gil Katz*,,
  3. Achia Urbach,
  4. Maya Schuldiner,
  5. Gal Markel,
  6. Joseph Itskovitz-Eldor§,
  7. Benjamin Reubinoff,
  8. Ofer Mandelboim,, and
  9. Nissim Benvenisty,
  1. Department of Genetics, Silberman Institute of Life Sciences, Hebrew University, 91904 Jerusalem, Israel; The Lautenberg Center for General and Tumor Immunology, Hadassah Medical School, Hebrew University, 91120 Jerusalem, Israel; §Department of Obstetrics and Gynecology, Rambam Medical Center, Faculty of Medicine, The Technion, Haifa 31096, Israel; and The Goldyne Savad Institute of Gene Therapy, Hadassah University Hospital, 91120 Jerusalem, Israel
  1. Communicated by Philip Leder, Harvard Medical School, Boston, MA (received for review March 13, 2002)

Abstract

Human embryonic stem (ES) cells are pluripotent cells that may be used in transplantation medicine. These cells can be induced to differentiate into cells from the three embryonic germ layers both in vivo and in vitro. To determine whether human ES cells might be rejected after transplantation, we examined cell surface expression of the MHC proteins in these cells. Our results show very low expression levels of MHC class I (MHC-I) proteins on the surface of human ES cells that moderately increase on in vitro or in vivo differentiation. A dramatic induction of MHC-I proteins was observed when the cells were treated with IFN-γ but not with IFN-α or -β. However, all three IFNs induced expression of MHC-I proteins in differentiated human ES cells. MHC-II proteins and HLA-G were not expressed on the surface of undifferentiated or differentiated cells. Ligands for natural killer cell receptors were either absent or expressed in very low levels in human ES cells and in their differentiated derivatives. In accordance, natural killer cytotoxic assays demonstrated only limited lysis of both undifferentiated and differentiated cells. To initiate a histocompatibility databank of human ES cells, we have isotyped several of the published ES cell lines for their human leukocyte antigens. In conclusion, our results demonstrate that human ES cells can express high levels of MHC-I proteins and thus may be rejected on transplantation.

Footnotes

  • * M.D. and G.K. contributed equally to this work.

  • To whom reprint requests should be addressed. E-mail: nissimb{at}mail.ls.huji.ac.il or oferman{at}md2.huji.ac.il.

  • Abbreviations:
    ES,
    embryonic stem;
    ICM,
    inner cell mass;
    EBs,
    embryoid bodies;
    CTL,
    cytotoxic T lymphocytes;
    NK,
    natural killer
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