B lymphocyte chemotaxis regulated in association with microanatomic localization, differentiation state, and B cell receptor engagement

J Exp Med. 1998 Mar 2;187(5):753-62. doi: 10.1084/jem.187.5.753.

Abstract

Migration of mature B lymphocytes within secondary lymphoid organs and recirculation between these sites are thought to allow B cells to obtain T cell help, to undergo somatic hypermutation, to differentiate into effector cells, and to home to sites of antibody production. The mechanisms that direct migration of B lymphocytes are unknown, but there is evidence that G protein-coupled receptors, and possibly chemokine receptors, may be involved. Stromal cell- derived factor (SDF)-1alpha is a CXC chemokine previously characterized as an efficacious chemoattractant for T lymphocytes and monocytes in peripheral blood. Here we show with purified tonsillar B cells that SDF-1alpha also attracts naive and memory, but not germinal center (GC) B lymphocytes. Furthermore, GC B cells could be converted to respond to SDF-1alpha by in vitro differentiation into memory B lymphocytes. Conversely, the migratory response in naive and memory B cells was significantly reduced after B cell receptor engagement and CD40 signaling. The receptor for SDF-1, CXC chemokine receptor 4 (CXCR4), was found to be expressed on responsive as well as unresponsive B cell subsets, but was more rapidly downregulated on responsive cells by ligand. Finally, messenger RNA for SDF-1 was detected by in situ hybridization in a layer of cells surrounding the GC. These findings show that responsiveness to the chemoattractant SDF-1alpha is regulated during B lymphocyte activation, and correlates with positioning of B lymphocytes within a secondary lymphoid organ.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / metabolism
  • B-Lymphocytes / physiology*
  • Cell Differentiation
  • Cells, Cultured
  • Chemokine CXCL12
  • Chemokines / physiology*
  • Chemokines, CXC*
  • Chemotaxis, Leukocyte / immunology*
  • Down-Regulation
  • Gene Expression
  • Humans
  • Immunologic Memory
  • Immunophenotyping
  • Lymphocyte Activation
  • Palatine Tonsil / cytology
  • RNA, Messenger / genetics
  • Receptor Aggregation
  • Receptors, Antigen, B-Cell / immunology*
  • Receptors, CXCR4 / metabolism

Substances

  • Actins
  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines
  • Chemokines, CXC
  • RNA, Messenger
  • Receptors, Antigen, B-Cell
  • Receptors, CXCR4