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The Journal of Immunology, 1998, 161: 4472-4475.
Copyright © 1998 by The American Association of Immunologists


CUTTING EDGE

Cutting Edge: Senescent BALB/c Mice Exhibit Decreased Expression of {lambda}5 Surrogate Light Chains and Reduced Development Within the Pre-B Cell Compartment1

Erin M. Sherwood, Bonnie B. Blomberg, Wei Xu, Cynthia A. Warner and Richard L. Riley2

* Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL 33101

Although senescent BALB/c mice (~2 years old) have reduced numbers of small pre-B cells, early pre-B cells (CD43+CD25+B220+) are present in comparable numbers within the bone marrow of both young (3–6-month-old) and senescent BALB/c mice. The transition of CD43+ pre-B cells to the CD43- pre-B cell compartments is dependent on proliferation and clonal maturation dictated by the pre-B cell receptor (µ/{lambda}5/VpreB). In vivo, senescent CD43+B220+ pro-B/early pre-B cells demonstrated reduction of {lambda}5 mRNA, by RT-PCR analysis, and of both surface and cytoplasmic {lambda}5 protein. Decreased {lambda}5 protein expression was also seen among pro-B/pre-B cells derived from senescent bone marrow after stimulation in vitro with IL-7. We propose that diminished expression of the {lambda}5 surrogate light chain results in decreased pre-B cell receptor formation and contributes to reduced recruitment of nascent CD43+ pre-B cells into the CD43- large and small pre-B cell compartments.







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