Normal development of mice deficient in beta 2M, MHC class I proteins, and CD8+ T cells

Science. 1990 Jun 8;248(4960):1227-30. doi: 10.1126/science.2112266.

Abstract

Major histocompatibility class I proteins display viral and self antigens to potentially responsive cells and are important for the maturation of T cells; beta 2-microglobulin (beta 2M) is required for their normal expression. Mouse chimeras derived from embryonic stem cells with a disrupted beta 2M gene transmitted the inactivated gene to their progeny. Animals homozygous for the mutated beta 2M gene were obtained at expected frequencies after further breeding. The homozygotes appeared normal, although no class I antigens could be detected on their cells and the animals are grossly deficient in CD4- CD8+ T cells, which normally mediate cytotoxic T cell function.

Publication types

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

MeSH terms

  • Animals
  • Antigens, Differentiation, T-Lymphocyte / genetics*
  • CD4 Antigens / genetics
  • CD8 Antigens
  • Chimera
  • Gene Expression
  • Genes
  • Genes, MHC Class I
  • Histocompatibility Antigens Class I / genetics*
  • Lymph Nodes / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Mutation*
  • Spleen / immunology
  • T-Lymphocytes / immunology*
  • beta 2-Microglobulin / deficiency*
  • beta 2-Microglobulin / genetics

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • CD4 Antigens
  • CD8 Antigens
  • Histocompatibility Antigens Class I
  • beta 2-Microglobulin