| Literature DB >> 18981099 |
Chie Watanabe1, Geraldine L Shu, Timothy S Zheng, Richard A Flavell, Edward A Clark.
Abstract
Caspase (Casp) family proteases regulate not only lymphocyte apoptosis but also lymphocyte activation and development. In this study, we show that Casp6 regulates B cell activation and differentiation into plasma cells by modifying cell cycle entry. B cells from Casp6 knockout (Casp6 KO) mice examined ex vivo have more cells in G(1) than wild-type B cells, and mitogen-induced G(1) entry of Casp6 KO B cells is much faster than that of wild-type B cells. Even so, S phase entry and proliferation are not increased in Casp6 KO B cells. Rather than proliferating, activated Casp6 KO B cells preferentially differentiate into syndecan-1(+) plasma cells and produce Abs. In Casp6 KO mice compared with WT mice, serum levels of IgG1, IgG2a, and IgG2b are increased and Ag-specific Ab responses are also enhanced along with increased percentages of syndecan-1(+) plasma cells. Casp6 may regulate both B cell activation and differentiation by modifying requirements for G(0) B cells to enter G(1).Entities:
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Year: 2008 PMID: 18981099 PMCID: PMC2728076 DOI: 10.4049/jimmunol.181.10.6810
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422