4.6 Article

Caspase-6 Regulates B Cell Activation and Differentiation into Plasma Cells

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JOURNAL OF IMMUNOLOGY
卷 181, 期 10, 页码 6810-6819

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.181.10.6810

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  1. National Institutes of Health [GM37905, DE16381, RR00166]
  2. Japan Society

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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). The Journal of Immunology, 2008, 181: 6810-6819.

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