The cytoplasmic domain of CD8 beta regulates Lck kinase activation and CD8 T cell development

J Immunol. 1998 Jul 1;161(1):183-91.

Abstract

Previous studies have shown that CD8 beta plays a role in both enhancing CD8 alpha-associated Lck kinase activity and promoting the development of CD8-lineage T cells. To examine the role of this enhancement in the maturation of CD8-lineage cells, we assessed CD8 alpha-associated Lck kinase activity in both T cell hybridomas and thymocytes of mice expressing CD8 beta mutations known to impair CD8 T cell development. Lack of CD8 beta expression or expression of a cytoplasmic domain-deleted CD8 beta resulted in a severalfold reduction in CD8 alpha-associated Lck kinase activity compared with that observed with cells expressing wild-type CD8 beta chain. This analysis indicated a critical role for the cytoplasmic domain of CD8 beta in the regulation of CD8 alpha-associated Lck activity. Decreased CD8 alpha-associated Lck activity observed with the various CD8 beta mutations also correlated with diminished in vivo cellular tyrosine phosphorylation. In addition, analysis of CD8 beta mutant mice (CD8 beta-/- or cytoplasmic domain-deleted CD8 beta transgenic) indicated that the degree of reduction in CD8 alpha-associated Lck activity associated with each mutation correlated with the severity of developmental impairment. These results support the importance of CD8 beta-mediated enhancement of CD8 alpha-associated Lck kinase activity in the differentiation of CD8 single-positive thymocytes.

Publication types

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

MeSH terms

  • Animals
  • CD8 Antigens / biosynthesis
  • CD8 Antigens / genetics
  • CD8 Antigens / physiology*
  • CD8-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / enzymology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Differentiation / immunology
  • Cell Line
  • Cytoplasm / enzymology
  • Cytoplasm / immunology*
  • Enzyme Activation / immunology
  • Genetic Vectors / biosynthesis
  • Genetic Vectors / immunology
  • Humans
  • Hybridomas / metabolism
  • Intracellular Fluid / enzymology
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / immunology
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / metabolism*
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Phosphorylation
  • Protein Structure, Tertiary
  • Sequence Deletion / immunology
  • Substrate Specificity
  • Tyrosine / metabolism

Substances

  • CD8 Antigens
  • Tyrosine
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck)