T cell-B cell thymic cross-talk: maintenance and function of thymic B cells requires cognate CD40-CD40 ligand interaction

J Immunol. 2014 Dec 1;193(11):5534-44. doi: 10.4049/jimmunol.1401655. Epub 2014 Oct 24.

Abstract

Thymic development requires bidirectional interaction or cross-talk between developing T cells and thymic stromal cells, a relationship that has been best characterized for the interaction between thymocytes and thymic epithelial cells. We have characterized in this article the requirement for similar cross-talk in the maintenance and function of thymic B cells, another population that plays a role in selection of developing thymic T cells. We found that maintenance of thymic B cells is strongly dependent on the presence of mature single-positive thymocytes and on the interactions of these T cells with specific Ag ligand. Maintenance of thymic B cell number is strongly dependent on B cell-autonomous expression of CD40, but not MHC class II, indicating that direct engagement of CD40 on thymic B cells is necessary to support their maintenance and proliferation. Thymic B cells can mediate negative selection of superantigen-specific, self-reactive, single-positive thymocytes, and we show that CD40 expression on B cells is critical for this negative selection. Cross-talk with thymic T cells is thus required to support the thymic B cell population through a pathway that requires cell-autonomous expression of CD40, and that reciprocally functions in negative selection of autoreactive T cells.

Publication types

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

MeSH terms

  • Animals
  • Autoantigens / immunology
  • B-Lymphocytes / immunology*
  • CD40 Antigens / genetics
  • CD40 Antigens / metabolism*
  • CD40 Ligand / genetics
  • CD40 Ligand / metabolism*
  • Cell Communication
  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Protein Binding / genetics
  • T-Lymphocytes / immunology*
  • Thymus Gland / immunology*

Substances

  • Autoantigens
  • CD40 Antigens
  • CD40 Ligand