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*Substance via MeSH
The Journal of Immunology, 1998, 161: 1132-1139.
Copyright © 1998 by The American Association of Immunologists

Surrogate Light Chain Production During B Cell Differentiation: Differential Intracellular Versus Cell Surface Expression1

Yui-Hsi Wang*, Jun Nomura*,{ddagger}, Ona Marie Faye-Petersen{dagger} and Max D. Cooper2,*,{dagger},{ddagger}

* Division of Developmental and Clinical Immunology; Departments of Medicine, Pediatrics, Microbiology, and {dagger} Pathology; and {ddagger} Howard Hughes Medical Institute, University of Alabama, Birmingham, AL 35924

Expression of the surrogate light ({psi}L) chain genes encoding the VpreB and {lambda}5/14.1 proteins is restricted to B-lineage cells. Pro-B and pre-B cells produce {psi}L chains, but whether both employ these as cell surface receptor components remains enigmatic. Recombinant human VpreB protein was used to generate a large panel of monoclonal anti-VpreB Abs to examine this issue. Native {psi}L chain proteins within pro-B cells as well as those serving as receptor components on pre-B cells were precipitated by 16 of the 26 anti-VpreB Abs. Surrogate light chains were easily detected on pre-B cell lines, whereas these anti-VpreB Abs reacted with pro-B cell lines only after plasma membrane permeabilization. The subpopulation of normal bone marrow cells bearing pre-B receptors included large and small pre-B cells exclusively, although pro-B cells also contained intracellular VpreB. VpreB proteins were not detected on or within B cells in bone marrow or the circulation, but a subpopulation of B cells in germinal centers was found to express the VpreB proteins intracellularly. Surrogate L chains are thus intermittently produced during human B-lineage differentiation, while their role as receptor components appears limited to the pre-B cell stage.




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