Impaired Immunoproteasome Assembly and Immune Responses in PA28 −/− Mice

Author:

Preckel Tobias1,Fung-Leung Wai-Ping1,Cai Zeling1,Vitiello Antonella1,Salter-Cid Luisa1,Winqvist Ola1,Wolfe Tom G.2,Herrath Matthias Von2,Angulo Ana2,Ghazal Peter2,Lee Jiing-Dwan2,Fourie Anne M.1,Wu Ying1,Pang Jesse1,Ngo Karen1,Peterson Per A.1,Früh Klaus1,Yang Young1

Affiliation:

1. The R. W. Johnson Pharmaceutical Research Institute, 3210 Merryfield Row, San Diego, CA 92121, USA.

2. The Scripps Research Institute, 10666 North Torrey Pines Road, La Jolla, CA 92037, USA.

Abstract

In vitro PA28 binds and activates proteasomes . It is shown here that mice with a disrupted PA28b gene lack PA28a and PA28b polypeptides, demonstrating that PA28 functions as a hetero-oligomer in vivo. Processing of antigenic epitopes derived from exogenous or endogenous antigens is altered in PA28 –/– mice. Cytotoxic T lymphocyte responses are impaired, and assembly of immunoproteasomes is greatly inhibited in mice lacking PA28. These results show that PA28 is necessary for immunoproteasome assembly and is required for efficient antigen processing, thus demonstrating the importance of PA28-mediated proteasome function in immune responses.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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