Regulation of promoter and intron enhancer activity in immunoglobulin heavy-chain genes during B-cell differentiation

Microbiol Immunol. 1998;42(5):399-405. doi: 10.1111/j.1348-0421.1998.tb02301.x.

Abstract

Chloramphenicol acetyltransferase (CAT) transgenic mice, in which the transgene is regulated by the VH promoter and heavy-chain intron enhancer (E mu), were examined to investigate the variation of activity of these cis-acting elements during the late stage of B-cell development. CAT enzyme activity decreased when resting B cells were stimulated through B-cell receptors (BCR) with goat anti-mouse IgM antibodies in vitro. On the other hand, when these B cells were stimulated by lipopolysaccharide (LPS) in vitro, they showed enhanced CAT activity, accompanied by an increase in the number of CD43+ B220+ cells (pro-plasma and plasma cells). In addition, the CAT activities in CD43+ B220+ and PNAhi B220+ cells from immunized mice were higher than those in CD43- B220+ and PNAlo B220+ cells, respectively. These results suggest that the activity of E mu in the context of VH promoter was transiently down-regulated by stimulation through the BCR but enhanced at the pro-plasma and plasma stages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes* / cytology
  • B-Lymphocytes* / drug effects
  • Cell Count
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics*
  • Cells, Cultured
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Genes, Immunoglobulin / genetics*
  • Immunoglobulin M / pharmacology
  • Introns / genetics*
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Transgenic
  • Plasma Cells / immunology
  • Spleen

Substances

  • Immunoglobulin M
  • Lipopolysaccharides
  • Chloramphenicol O-Acetyltransferase