Baff Binds to the Tumor Necrosis Factor Receptor–Like Molecule B Cell Maturation Antigen and Is Important for Maintaining the Peripheral B Cell Population

Author:

Thompson Jeffrey S.1,Schneider Pascal2,Kalled Susan L.3,Wang LiChun3,Lefevre Eric A.4,Cachero Teresa G.5,MacKay Fabienne6,Bixler Sarah A.1,Zafari Mohammad3,Liu Zhong-Ying3,Woodcock Stephen A.3,Qian Fang5,Batten Marcel6,Madry Christine4,Richard Yolande4,Benjamin Christopher D.3,Browning Jeffrey L.3,Tsapis Andreas4,Tschopp Jurg2,Ambrose Christine1

Affiliation:

1. Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142

2. Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland

3. Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142

4. Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France

5. Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142

6. Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia

Abstract

The tumor necrosis factor (TNF) family member B cell activating factor (BAFF) binds B cells and enhances B cell receptor–triggered proliferation. We find that B cell maturation antigen (BCMA), a predicted member of the TNF receptor family expressed primarily in mature B cells, is a receptor for BAFF. Although BCMA was previously localized to the Golgi apparatus, BCMA was found to be expressed on the surface of transfected cells and tonsillar B cells. A soluble form of BCMA, which inhibited the binding of BAFF to a B cell line, induced a dramatic decrease in the number of peripheral B cells when administered in vivo. Moreover, culturing splenic cells in the presence of BAFF increased survival of a percentage of the B cells. These results are consistent with a role for BAFF in maintaining homeostasis of the B cell population.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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