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International Immunology, Vol. 13, No. 4, 553-558, April 2001
© 2001 Japanese Society for Immunology

Alterations in peripheral B cells and B cell progenitors following androgen ablation in mice

Thomas M. Ellis, Michael T. Moser, Phong T. Le, Robert C. Flanigan and Eugene D. Kwon

Departments of Medicine, Urology, and Cell Biology, Neurobiology and Anatomy, Loyola University School of Medicine, 2160 South First Avenue Maywood, IL 60153, USA

Correspondence to: T. M. Ellis

The production of B lymphocytes is regulated in part by physiologic levels of androgens and estrogens. While these sex hormones down-regulate B lymphopoiesis, augmentation of B lymphopoiesis occurs under conditions where androgen or estrogen levels are decreased. In this study we examine the effect of androgen ablation of male mice on B lymphopoiesis and on the phenotypic composition of peripheral B lymphocyte populations. Spleen and thymic weights are significantly increased following castration, as is the total number of peripheral blood lymphocytes. However, the absolute numbers of B cells in the periphery are selectively increased following castration; the numbers of T cells, NK cells and granulocytes remain unchanged. The increase in circulating B cells is due largely to increases in the numbers of recent bone marrow emigrants expressing a B220lo+CD24hi+ phenotype and these cells remain significantly elevated in castrated mice for up to 54 days post-castration. Similar increases in the percentages of newly emigrated B cells are observed in mice that lack a functional androgen receptor (Tfm). Finally, assessments of B cell progenitors in the bone marrow revealed significant increases in the relative numbers of IL-7-responsive B cell progenitors, including cells in Hardy fractions B (early pro-B cells), C (late pro-B cells), D (pre-B cells) and E (immature B cells). These findings demonstrate that androgen ablation following castration significantly and selectively alters the composition of peripheral B cells in mice. Further, these alterations result from the potentiating effects of androgen ablation on IL-7-responsive pro-B cell progenitors.

Keywords: androgen ablation, B cell, B cell progenitor

Transmitting editor: J. P. Allison


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