Transgenic mice expressing dominant-negative bright exhibit defects in B1 B cells

J Immunol. 2008 Nov 15;181(10):6913-22. doi: 10.4049/jimmunol.181.10.6913.

Abstract

The transcription factor Bright up-regulates Ig H chain production from select V region promoters and requires Bright dimerization, Bruton's tyrosine kinase (Btk), and the Btk substrate, TFII-I, for this activity. Defects in Btk cause X-linked immunodeficiency disease in mice and humans. Btk-deficient mice exhibit decreased serum IgM production, B cell developmental blocks, absence of peritoneal B1 cells, and subnormal immune responses against Ags, including phosphorylcholine, which confer protection against Streptococcus pneumoniae. Transgenic mice expressing dominant-negative Bright share similarities with Btk-deficient mice, including decreased serum IgM, poor anti-phosphorylcholine responses, and slightly reduced numbers of mature B cells. Although dominant-negative Bright mice developed B1 B cells, these were functionally deficient in Ig secretion. These data suggest a mechanistic explanation for the abnormal responses to phosphorylcholine observed in Btk-deficient mice, and indicate that Bright functions in a subset of Btk-dependent pathways in vivo, particularly those responses dominated by B1 B cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Agammaglobulinaemia Tyrosine Kinase
  • Amino Acid Sequence
  • Animals
  • Antibodies / blood
  • Antigens, CD19 / genetics
  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocytes / immunology*
  • Blotting, Western
  • DNA-Binding Proteins
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flow Cytometry
  • Humans
  • Immunohistochemistry
  • Lymphocyte Activation / immunology
  • Male
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Oncogenes / genetics*
  • Promoter Regions, Genetic
  • Protein-Tyrosine Kinases
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocytes / immunology
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism*
  • Transcription Factors

Substances

  • Antibodies
  • Antigens, CD19
  • Arid3a protein, mouse
  • DNA-Binding Proteins
  • Trans-Activators
  • Transcription Factors
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • BTK protein, human
  • Btk protein, mouse