Variation in MHC expression between undifferentiated mouse ES cells and ES cell-derived insulin-producing cell clusters

Transplantation. 2009 May 15;87(9):1300-4. doi: 10.1097/TP.0b013e3181a19421.

Abstract

Background: The progeny of embryonic stem (ES) cells may eventually be used to replace damaged tissues in transplantation, yet their immunogenicity remains ill-defined. The major histocompatibility complex (MHC) is a determinant of immunogenicity in transplantation.

Methods and results: Herein, we show differences in MHC expression between mouse ES cells and ES cell derived insulin producing cell clusters (IPCCs), including a relatively higher expression of MHC Class I in IPCCs and a faster, more dramatic induction of MHC Class I in IPCCs following challenge with interferon-gamma (IFN-gamma). MHC Class II was induced on IPCCs, but not ES cells, after exposure to IFN-gamma. Transplantation of syngeneic or allogeneic IPCCs was insufficient to trigger up-regulation of MHC class I within three days after transplantation.

Discussion: These data highlight differences in MHC expression between ES cells and a fully differentiated ES cell derived tissue and suggest how the progeny of ES cells may be susceptible to rejection after transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / immunology
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / drug effects
  • Embryonic Stem Cells / immunology*
  • Embryonic Stem Cells / physiology
  • Histocompatibility Antigens Class I / biosynthesis
  • Homeostasis
  • Insulin / biosynthesis*
  • Interferon-gamma / pharmacology
  • Major Histocompatibility Complex*
  • Mice

Substances

  • Histocompatibility Antigens Class I
  • Insulin
  • Interferon-gamma