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International Immunology, Vol. 15, No. 10, pp. 1137-1147, October 2003
© 2003 Japanese Society for Immunology


FEATURED ARTICLE OF THE MONTH

Transitional and marginal zone B cells have a high proportion of unmasked CD22: implications for BCR signaling

Claus-Peter Danzer1,3, Brian E. Collins2, Ola Blixt2, James C. Paulson2 and Lars Nitschke1

1 Institute of Virology and Immunobiology, University of Würzburg, Versbacherstrasse 7, 97078 Würzburg, Germany 2 Department of Molecular Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92075, USA 3 Present address: Novartis Pharma, Lichtstrasse 35, 4056 Basel, Switzerland

Correspondence to: L. Nitschke; E-mail: nitschke{at}vim.uni-wuerzburg.de
Transmitting editor: S. Izui

CD22, a B cell-specific member of the Siglec family, is an important inhibitor of B cell signaling. The first Ig-like domain of CD22 specifically binds to {alpha}2,6-linked sialic acids. Through these interactions CD22 can mediate adhesion to other cells in trans, but can also bind endogenous ligands on the B cell surface in cis. Cis binding of CD22 to sialylated ligands enhances the efficiency of inhibition and thereby reduces the BCR signaling strength. In this study we used a newly developed oligomeric streptavidin-based sialylated probe as an artificial CD22 ligand. We found that CD22 is bound to ligands in cis on most B cells. However, there is a proportion of B cells with unbound (unmasked) CD22. The subpopulation with unmasked CD22 is 2-fold increased in transitional and marginal zone B cells in the spleen and on B1 cells in the peritoneum, when compared to mature B cells. Also, B cells with unmasked CD22 have an activated phenotype. Unmasking of CD22 could be functionally involved in lowering the signaling threshold on developmental checkpoints such as transitional B cells and during B cell activation or could be a consequence of such activation processes.

Keywords: B lymphocyte, CD22, sialic acid, Siglec


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