The TACI receptor regulates T-cell-independent marginal zone B cell responses through innate activation-induced cell death

Immunity. 2013 Sep 19;39(3):573-83. doi: 10.1016/j.immuni.2013.05.019. Epub 2013 Sep 5.

Abstract

Activation-induced cell death (AICD) plays a critical role in immune homeostasis and tolerance. In T-cell-dependent humoral responses, AICD of B cells is initiated by Fas ligand (FasL) on T cells, stimulating the Fas receptor on B cells. In contrast, T-cell-independent B cell responses involve innate-type B lymphocytes, such as marginal zone (MZ) B cells, and little is known about the mechanisms that control AICD during innate B cell responses to Toll-like receptor (TLR) activation. Here, we show that MZ B cells undergo AICD in response to TLR4 activation in vivo. The transmembrane activator, calcium modulator, and cyclophilin ligand interactor (TACI) receptor and TLR4 cooperate to upregulate expression of both FasL and Fas on MZ B cells and also to repress inhibitors of Fas-induced apoptosis signaling. These findings demonstrate an unappreciated role for TACI and its ligands in the regulation of AICD during T-cell-independent B cell responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • B-Cell Activation Factor Receptor / biosynthesis
  • B-Lymphocytes / immunology
  • Enzyme Activation
  • Fas Ligand Protein / biosynthesis
  • Fas Ligand Protein / metabolism*
  • Lipopolysaccharides
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Toll-Like Receptor 4 / metabolism*
  • Transmembrane Activator and CAML Interactor Protein / genetics
  • Transmembrane Activator and CAML Interactor Protein / metabolism*
  • fas Receptor / metabolism*

Substances

  • B-Cell Activation Factor Receptor
  • Fas Ligand Protein
  • Fas protein, mouse
  • Fasl protein, mouse
  • Lipopolysaccharides
  • Tlr4 protein, mouse
  • Tnfrsf13b protein, mouse
  • Tnfrsf13c protein, mouse
  • Toll-Like Receptor 4
  • Transmembrane Activator and CAML Interactor Protein
  • fas Receptor