CCR3 expression induced by IL-2 and IL-4 functioning as a death receptor for B cells

J Immunol. 2003 Aug 15;171(4):1722-31. doi: 10.4049/jimmunol.171.4.1722.

Abstract

We report that CCR3 is not expressed on freshly isolated peripheral and germinal B cells, but is up-regulated after stimulation with IL-2 and IL-4 (approximately 98% CCR3(+)). Ligation of CCR3 by eotaxin/chemokine ligand (CCL) 11 induces apoptosis in IL-2- and IL-4-stimulated primary CD19(+) (approximately 40% apoptotic cells) B cell cultures as well as B cell lines, but has no effect on chemotaxis or cell adhesion. Freshly isolated B cells express low levels of CD95 and CD95 ligand (CD95L) (19 and 21%, respectively). Expression is up-regulated on culture in the presence of a combination of IL-2, IL-4, and eotaxin/CCL11 (88% CD95 and 84% CD95L). We therefore propose that ligation of such newly induced CCR3 on peripheral and germinal B cells by eotaxin/CCL11 leads to the enhanced levels of CD95 and CD95L expression. Ligation of CD95 by its CD95L expressed on neigboring B cells triggers relevant death signaling pathways, which include an increase in levels of Bcl-2 expression, its functional activity, and the release of cytochrome c from the mitochondria into the cytosol. These events initiate a cascade of enzymatic processes of the caspase family, culminating in programmed cell death. Interaction between CCR3 and eotaxin/CCL11 may, besides promoting allergic reactions, drive activated B cells to apoptosis, thereby reducing levels of Ig production, including IgE, and consequently limit the development of the humoral immune response. The apoptotic action of eotaxin/CCL11 suggests a therapeutic modality in the treatment of B cell lymphoma.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / immunology*
  • B-Lymphocyte Subsets / cytology*
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / metabolism*
  • Cell Adhesion / immunology
  • Cell Line
  • Cells, Cultured
  • Chemokine CCL11
  • Chemokines, CC / pharmacology
  • Chemotaxis, Leukocyte / immunology
  • Child
  • Fas Ligand Protein
  • Humans
  • Interleukin-2 / pharmacology*
  • Interleukin-4 / pharmacology*
  • Ligands
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / physiology
  • Palatine Tonsil
  • Receptors, CCR3
  • Receptors, Chemokine / biosynthesis*
  • Receptors, Chemokine / physiology*
  • Receptors, Tumor Necrosis Factor / biosynthesis
  • Receptors, Tumor Necrosis Factor / physiology*
  • Tumor Cells, Cultured
  • fas Receptor / immunology
  • fas Receptor / metabolism
  • fas Receptor / physiology

Substances

  • CCL11 protein, human
  • CCR3 protein, human
  • Chemokine CCL11
  • Chemokines, CC
  • FASLG protein, human
  • Fas Ligand Protein
  • Interleukin-2
  • Ligands
  • Membrane Glycoproteins
  • Receptors, CCR3
  • Receptors, Chemokine
  • Receptors, Tumor Necrosis Factor
  • fas Receptor
  • Interleukin-4