Critical roles for the Bcl-3 oncoprotein in T cell-mediated immunity, splenic microarchitecture, and germinal center reactions.

Journal:

Immunity 1997 Apr

Authors:

Franzoso G, Carlson L, Scharton-Kersten T, Shores EW, Epstein S, Grinberg A, Tran T, Shacter E, Leonardi A, Anver M, Love P, Sher A, Siebenlist U

Abstract

Chromosomal translocations of bcl-3 are associated with chronic B cell lymphocytic leukemias. Previously, we have shown that Bcl-3, a distinct member of the I kappa B family, may function as a positive regulator of NF-kappa B activity, although its physiologic roles remained unknown. To uncover these roles, we generated Bcl-3-deficient mice. Mutant mice, but not their littermate controls, succumb to T. gondii owing to failure to mount a protective T helper 1 immune response. Bcl-3-deficient mice
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are also impaired in germinal center reactions and T-dependent antibody responses to influenza virus. The results reveal critical roles for Bcl-3 in antigen-specific priming of T and B cells. Altered microarchitecture of secondary lymphoid organs in mutant mice, including partial loss of B cells, may underlie the immunologic defects. The implied role of Bcl-3 in maintaining B cells in wild-type mice may related to its oncogenic potential.[less]

Mesh Headings:

Animals, Antibodies, Viral, B-Lymphocyte Subsets, Cell Differentiation, Cell Line, Embryo, Mammalian, Germinal Center, Immunity, Cellular, Influenza A virus, Mice, Mice, Inbred Strains, Mice, Knockout, Proto-Oncogene Proteins, Proto-Oncogenes, Spleen, Stem Cells, T-Lymphocytes, Toxoplasmosis, Transcription Factors