Influence of SHIP on the NK repertoire and allogeneic bone marrow transplantation

Science. 2002 Mar 15;295(5562):2094-7. doi: 10.1126/science.1068438.

Abstract

Natural killer cell (NK) receptors for major histocompatibility complex (MHC) class I influence engraftment and graft-versus-tumor effects after allogeneic bone marrow transplantation. We find that SH2-containing inositol phosphatase (SHIP) influences the repertoire of NK receptors. In adult SHIP-/- mice, the NK compartment is dominated by cells that express two inhibitory receptors capable of binding either self or allogeneic MHC ligands. This promiscuous repertoire has significant functional consequences, because SHIP-/- mice fail to reject fully mismatched allogeneic marrow grafts and show enhanced survival after such transplants. Thus, SHIP plays an important role in two processes that limit the success of allogeneic marrow transplantation: graft rejection and graft-versus-host disease.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Antigens, Ly*
  • Bone Marrow Transplantation / immunology*
  • Cell Survival
  • Graft Rejection / immunology*
  • Graft Survival
  • Graft vs Host Disease / immunology*
  • H-2 Antigens / immunology
  • H-2 Antigens / metabolism
  • Haplotypes
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism
  • Killer Cells, Natural / enzymology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lectins, C-Type*
  • Ligands
  • Lymphocyte Count
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred A
  • Mice, Inbred BALB C
  • NK Cell Lectin-Like Receptor Subfamily D
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
  • Phosphoric Monoester Hydrolases / chemistry
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • Phosphorylation
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Receptors, Immunologic / metabolism
  • Receptors, NK Cell Lectin-Like
  • Signal Transduction
  • Transplantation, Homologous
  • src Homology Domains

Substances

  • Antigens, CD
  • Antigens, Ly
  • H-2 Antigens
  • Histocompatibility Antigens Class I
  • Lectins, C-Type
  • Ligands
  • Membrane Glycoproteins
  • NK Cell Lectin-Like Receptor Subfamily D
  • Proto-Oncogene Proteins
  • Receptors, Immunologic
  • Receptors, NK Cell Lectin-Like
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Phosphoric Monoester Hydrolases
  • INPPL1 protein, human
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases