Essential Immunoregulatory Role for BCAP in B Cell Development and Function

Author:

Yamazaki Tetsuo1,Takeda Kiyoshi2,Gotoh Kumiko13,Takeshima Hiroshi4,Akira Shizuo2,Kurosaki Tomohiro13

Affiliation:

1. Department of Molecular Genetics, Institute for Liver Research, Kansai Medical University

2. Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan

3. Laboratory for Lymphocyte Differentiation, RIKEN Research Center for Allergy and Immunology, 10-15 Fumizono-cho, Moriguchi, Osaka 570-8506, Japan

4. Division of Cell Biology, Institute of Life Science, Kurume University, Kurume, Fukuoka 839-0861, Japan

Abstract

BCAP was recently cloned as a binding molecule to phosphoinositide 3-kinase (PI3K). To investigate the role of BCAP, mutant mice deficient in BCAP were generated. While BCAP-deficient mice are viable, they have decreased numbers of mature B cells and B1 B cell deficiency. The mice produce lower titers of serum immunoglobulin (Ig)M and IgG3, and mount attenuated responses to T cell–independent type II antigen. Upon B cell receptor cross-linking, BCAP-deficient B cells exhibit reduced Ca2+ mobilization and poor proliferative responses. These findings demonstrate that BCAP plays a pivotal immunoregulatory role in B cell development and humoral immune responses.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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