The 90K Protein Increases Major Histocompatibility Complex Class I Expression and Is Regulated by Hormones, γ-Interferon, and Double-Strand Polynucleotides
Author(s) -
Antonino Grassadonia,
Nicola Tinari,
Bruno Fiorentino,
Koichi Suzuki,
Minoru Nakazato,
Michele De Tursi,
Cesidio Giuliani,
Giorgio Napolitano,
Dinah S. Singer,
Stefano Iacobelli,
Leonard D. Kohn
Publication year - 2004
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2004-0506
Subject(s) - biology , major histocompatibility complex , complementary dna , microbiology and biotechnology , interferon , transfection , antigen , polynucleotide , immune system , gene , immunology , biochemistry
Here we report the cloning of the rat 90K, a homolog of the mouse cyclophilin C-associated protein/mouse adherent macrophage and human 90K. The protein is constitutively expressed by FRTL-5 thyrocytes, and its levels are modulated by TSH, insulin/IGF-I, and gamma-interferon. Transfection of the cells with 90K cDNA or exposure to purified 90K resulted in a significant increase of the expression of major histocompatibility complex class I but not class II antigens. An increased expression of 90K was obtained after viral infection or introduction into the cells of fragments of viral, bacterial, or mammalian double-strand polynucleotides. The increase was sequence independent, not CpG mediated, and associated with the expression of molecules characterizing antigen-presenting-cell phenotype. The present data along with results from previous studies suggest that 90K plays an important role in the maintenance of an appropriate level of immune response.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom