The development of B lymphocytes from progenitor cells is dependent on the expression of a pre–B cell–specific receptor made up by a μ heavy chain associated with the surrogate light chains, immunoglobulin (Ig)α, and Igβ. A variant pre–B cell receptor can be formed in which the μ heavy chain is exchanged for a truncated μ chain denoted Dμ. To investigate the role of this receptor in the development of B cells, we have generated transgenic mice that express the Dμ protein in cells of the B lineage. Analysis of these mice reveal that Dμ expression leads to a partial block in B cell development at the early pre–B cell stage, probably by inhibiting VH to DHJH rearrangement. Furthermore, we provide evidence that Dμ induces VL to JL rearrangements.
Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ
We thank Drs. A. Cumano, J. Demengeot, B. Eriksson, and P. Perreira for discussions and for reviewing the manuscript.
This work was supported by a grant from the Swedish Natural Science Research Council.
Address correspondence to Dan Holmberg, Department of Immunology, Institut Pasteur, 25 rue de Dr. Roux, 750 15 Paris Cedex 15, France. Phone: 33-1-4568-8543 Fax: 33-1-4568-8921; E-mail: [email protected]
Abbreviations used in this paper: HSA, heat stable antigen; pBCR, pre–B cell receptor; RF, reading frame.
I. Bergqvist and U.-C. Tornberg contributed equally to this work.
Ulla-Carin Tornberg, Ingela Bergqvist, Matthias Haury, Dan Holmberg; Regulation of B Lymphocyte Development by the Truncated Immunoglobulin Heavy Chain Protein Dμ . J Exp Med 2 March 1998; 187 (5): 703–709. doi: https://doi.org/10.1084/jem.187.5.703
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