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Proteasomes are regulated by interferon gamma: implications for antigen processing.
Author(s) -
Young Mok Yang,
J.B. Waters,
Klaus Früh,
P A Peterson
Publication year - 1992
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.89.11.4928
Subject(s) - proteasome , antigen processing , major histocompatibility complex , antigen , biology , mhc class i , cytoplasm , interferon gamma , interferon , proteolysis , microbiology and biotechnology , antigen presentation , immune system , biochemistry , virology , t cell , genetics , enzyme
Class I major histocompatibility complex (MHC) molecules present antigenic peptides of cytoplasmic origin to T cells. As the lengths of these peptides seem restricted to eight or nine amino acids, an unusual proteolytic system must play a role in antigen processing. Proteasomes, a major extralysosomal proteolytic system, are responsible for the degradation of cytoplasmic proteins. We demonstrate that several proteasomal subunits, including MHC-encoded subunits, are regulated by interferon gamma. These data and the finding that MHC-encoded and other interferon gamma-regulated proteasomal subunits are uniquely associated with proteasomes strongly suggest that the immune system has recruited proteasomes for antigen processing.

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