Regulation of CD8 <sup>+</sup> T Cell Development by Thymus-Specific Proteasomes

Shigeo Murata(Toho University), Katsuhiro Sasaki(Toho University), Toshihiko Kishimoto(Toho University), Shin‐ichiro Niwa(Toho University), Hidemi Hayashi(Toho University), Yousuke Takahama(Toho University), Keiji Tanaka(Toho University)
Science
May 31, 2007
Cited by 566

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 beta5t. beta5t 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 beta5t into proteasomes in place of beta5 or beta5i selectively reduces this activity. We also found that beta5t-deficient mice displayed defective development of CD8(+) T cells in the thymus. Our results suggest a key role for beta5t in generating the MHC class I-restricted CD8(+) T cell repertoire during thymic selection.


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