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PMID: 9418137 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

CD79 alpha/CD79 beta heterodimers are expressed on pro-B cell surfaces without associated mu heavy chain.

International immunology ·Vol. 9 ·No. 11 ·1997-11-00 ·Pages 1767-72

Koyama M, Ishihara K, Karasuyama H, Cordell JL, Iwamoto A, Nakamura T

Abstract

During B cell development, the surface expression of CD79 alpha/CD79 beta heterodimers had been thought to begin in the pre-B cell stage where the heterodimers constitute pre-B cell receptors together with mu heavy and surrogate light chains. Thereafter, in mature B cells, CD79 alpha/CD79 beta associates with surface Ig to form B cell antigen receptors. In this study, we revealed by using newly established mAb that CD79 beta was expressed on the surface of pro-B cells which had not undergone the productive Ig gene rearrangement. Biochemical analysis showed that CD79 beta on pro-B cells existed either as monomers or as disulfide-linked heterodimers with CD79 alpha, non-covalently associated with four unidentified membrane molecules. Our finding that CD79 beta is expressed on earlier B-lineage cells than previously expected coincides with the recent study in which CD79 beta-deficient mice exhibit a blockade of B cell differentiation at the pro-B cell stage. Thus, it is speculated that the CD79 beta-containing complexes on pro-B cell surfaces may function to induce early B cell differentiation.

MeSH Terms
Animals Antibodies, Monoclonal Antigens, CD/biosynthesis,immunology,metabolism B-Lymphocytes/cytology,immunology,metabolism Bone Marrow Cells/cytology,metabolism CD79 Antigens Cell Line Cell Membrane/metabolism Dimerization Epitopes/analysis Immunoglobulin Heavy Chains/biosynthesis,metabolism Immunoglobulin mu-Chains/biosynthesis,metabolism Mice Receptors, Antigen, B-Cell/biosynthesis,immunology,metabolism
Chemicals
Antibodies, Monoclonal Antigens, CD CD79 Antigens Cd79a protein, mouse Epitopes Immunoglobulin Heavy Chains Immunoglobulin mu-Chains Receptors, Antigen, B-Cell
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Koyama M
Department of Infectious Diseases and Applied Immunology, University of Tokyo, Japan.
Ishihara K
Karasuyama H
Cordell J L
Iwamoto A
Nakamura T
Article Info
Journal
International immunology
Abbr.
Int Immunol
ISSN
0953-8178
Published
1997-11-00
Pages
1767-72
Language
English
Region
England
NLM ID
8916182
Subset
IM
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