Regulation of CD8 + T Cell Development by Thymus-Specific Proteasomes

Author:

Murata Shigeo12345,Sasaki Katsuhiro12345,Kishimoto Toshihiko12345,Niwa Shin-ichiro12345,Hayashi Hidemi12345,Takahama Yousuke12345,Tanaka Keiji12345

Affiliation:

1. Laboratory of Frontier Science, Core Technology and Research Center, Tokyo Metropolitan Institute of Medical Science, Bunkyo-ku, Tokyo 113-8613, Japan.

2. Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012, Japan.

3. Proteome Analysis Center, Faculty of Science, Toho University, Funabashi, Chiba 274-8510, Japan.

4. Department of Biomolecular Science, Faculty of Science, Toho University, Funabashi, Chiba 274-8510, Japan.

5. Link Genomics, Chuo-ku, Tokyo 103-0024, Japan.

Abstract

Proteasomes are responsible for generating peptides presented by the class I major histocompatibility complex (MHC) molecules of the immune system. Here, we report the identification of a previously unrecognized catalytic subunit called β5t. β5t is expressed exclusively in cortical thymic epithelial cells, which are responsible for the positive selection of developing thymocytes. Although the chymotrypsin-like activity of proteasomes is considered to be important for the production of peptides with high affinities for MHC class I clefts, incorporation of β5t into proteasomes in place of β5 or β5i selectively reduces this activity. We also found that β5t-deficient mice displayed defective development of CD8 + T cells in the thymus. Our results suggest a key role for β5t in generating the MHC class I–restricted CD8 + T cell repertoire during thymic selection.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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