Regulation of B Cell Differentiation and Plasma Cell Generation by IL-21, a Novel Inducer of Blimp-1 and Bcl-6

Katsutoshi Ozaki(National Heart Lung and Blood Institute), Rosanne Spolski(National Heart Lung and Blood Institute), Rachel Ettinger(National Institute of Arthritis and Musculoskeletal and Skin Diseases), Hyoung‐Pyo Kim(National Heart Lung and Blood Institute), Gang Wang(National Cancer Institute), Chen‐Feng Qi(National Institutes of Health), Patrick Hwu(Melanoma Institute Australia), Daniel J. Shaffer(Jackson Laboratory), Shreeram Akilesh(Jackson Laboratory), Derry C. Roopenian(Jackson Laboratory), Herbert C. Morse(National Institutes of Health), Peter E. Lipsky(National Institute of Arthritis and Musculoskeletal and Skin Diseases), Warren J. Leonard(National Heart Lung and Blood Institute)
The Journal of Immunology
November 1, 2004
Cited by 661Open Access
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Abstract

IL-21 is a type I cytokine whose receptor is expressed on T, B, and NK cells. Within the B cell lineage, IL-21 regulates IgG1 production and cooperates with IL-4 for the production of multiple Ab classes in vivo. Using IL-21-transgenic mice and hydrodynamics-based gene delivery of IL-21 plasmid DNA into wild-type mice as well as in vitro studies, we demonstrate that although IL-21 induces death of resting B cells, it promotes differentiation of B cells into postswitch and plasma cells. Thus, IL-21 differentially influences B cell fate depending on the signaling context, explaining how IL-21 can be proapoptotic for B cells in vitro yet critical for Ag-specific Ig production in vivo. Moreover, we demonstrate that IL-21 unexpectedly induces expression of both Blimp-1 and Bcl-6, indicating mechanisms as to how IL-21 can serve as a complex regulator of B cell maturation and terminal differentiation. Finally, BXSB-Yaa mice, which develop a systemic lupus erythematosus-like disease, have greatly elevated IL-21, suggesting a role for IL-21 in the development of autoimmune disease.


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