Antigen-receptor induced clonal expansion and deletion of lymphocytes are impaired in mice lacking HS1 protein, a substrate of the antigen-receptor-coupled tyrosine kinases

EMBO J. 1995 Aug 1;14(15):3664-78. doi: 10.1002/j.1460-2075.1995.tb00036.x.

Abstract

HS1, an intracellular protein expressed specifically in hematopoietic cells, is rapidly tyrosine phosphorylated after cross-linking of antigen receptors on B and T lymphocytes, implicating involvement of this molecule in the signal transduction pathways from the antigen receptors as a substrate of membrane-associated tyrosine kinase(s). The development of lymphoid cells in HS1-deficient mice, generated through gene targeting, appeared normal. However, antibody production to T-independent antigen and proliferative responses of splenic B and T cells after cross-linking of the antigen receptors were impaired in these mutant mice. Furthermore, B cells in the peritoneal cavity of the mutant mice were resistant to multivalent cross-linking of the antigen receptor, which causes apoptosis of such cells in normal mice. Crossing the HS1-deficient mice with the mice harboring transgenes encoding alpha and beta chains of T-cell antigen receptor against a male H-Y antigen resulted in a progeny that demonstrated a significantly impaired ability of thymic negative selection. These results indicate that HS1 is a novel molecule involved in the antigen-receptor-derived signaling pathways and plays important roles not only in clonal expansion, but also in clonal deletion of B and T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, T-Independent / metabolism
  • Apoptosis
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Base Sequence
  • Blood Proteins / physiology*
  • Cell Division
  • Clonal Deletion / immunology*
  • Ficoll / analogs & derivatives
  • Ficoll / metabolism
  • Gene Targeting
  • Lymphoid Tissue / growth & development
  • Lymphoid Tissue / immunology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Peritoneal Cavity
  • Phosphorylation
  • Protein-Tyrosine Kinases
  • Receptors, Antigen, B-Cell / metabolism*
  • Receptors, Antigen, T-Cell / metabolism*
  • Signal Transduction
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*
  • Trinitrobenzenes / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, T-Independent
  • Blood Proteins
  • HCLS1 protein, human
  • Receptors, Antigen, B-Cell
  • Receptors, Antigen, T-Cell
  • TNP-ficoll
  • Trinitrobenzenes
  • Ficoll
  • Protein-Tyrosine Kinases