Abstract:
:The class II transactivator (CIITA) controls both the constitutive and IFN-gamma inducible expression of HLA-D genes. In addition, through the squelching of another transactivator CREB-binding protein, CIITA was more recently shown to have a wider cellular function, including cell cycle control or cellular response to IFN-gamma and IL-4. However, due to its low expression level, its analysis mainly relies on the study of recombinant overexpressed forms of the protein. We report here the analysis of native CIITA in various cell types. We first show the precise timing of CIITA protein expression in a fibroblast cell line in response to IFN-gamma. This expression is observed 2 h after the cytokine addition with a peak of expression ranging from 16 to 24 h. We next show the existence of two major isoforms of the CIITA protein differentially expressed in fibroblast, B lymphocyte or melanoma cell lines. We present the first demonstration that these isoforms originate from alternative translation initiation codons. We finally show that CIITA isoforms translocate to the nucleus with an apparently similar efficiency. Our data therefore demonstrate the existence of CIITA isoforms whose respective ratio depends on the cell type examined. However, we present evidence for a modulation of this ratio in a melanoma cell line with an abnormal constitutive expression of MHC class II molecules.
journal_name
Int Immunoljournal_title
International immunologyauthors
Barbieri G,Deffrennes V,Prod'homme T,Vedrenne J,Baton F,Cortes C,Fischer A,Bono MR,Lisowska-Grospierre B,Charron D,Alcaïde-Loridan Cdoi
10.1093/intimm/dxf060subject
Has Abstractpub_date
2002-08-01 00:00:00pages
839-48issue
8eissn
0953-8178issn
1460-2377journal_volume
14pub_type
杂志文章abstract::The efficacy of cytotoxic T lymphocytes (CTL) has been shown to be highly dependent upon their functional avidity (the sensitivity of their cellular response to MHC-peptide complexes). To examine this relationship, we employed target cell lysis as a quantitative measure and established a set of four CTL clones that ex...
journal_title:International immunology
pub_type: 杂志文章
doi:10.1093/intimm/13.6.817
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journal_title:International immunology
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