Peroxisome Proliferator-Activated Receptor γ-Regulated Cathepsin D Is Required for Lipid Antigen Presentation by Dendritic Cells
Author(s) -
Britt Nakken,
Tamás Varga,
István Szatmári,
Lajos Széles,
Adrienn Gyöngyösi,
Petr A. Illarionov,
Balázs Dezsö,
Péter Gogolák,
Éva Rajnavölgyi,
László Nagy
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1002421
Subject(s) - lipid metabolism , microbiology and biotechnology , cd1d , antigen presentation , chemistry , lipid signaling , peroxisome proliferator activated receptor , transcription factor , antigen processing , peroxisome , biology , receptor , biochemistry , natural killer t cell , in vitro , gene , cytotoxic t cell
It is well established that dendritic cells (DCs) take up, process, and present lipid Ags in complex with CD1d molecules to invariant NKT cells. The lipid-activated transcription factor, peroxisome proliferator-activated receptor γ (PPARγ), has previously been shown to regulate CD1d expression in human monocyte-derived DCs, providing a link between lipid metabolism and lipid Ag presentation. We report that PPARγ regulates the expression of a lysosomal protease, cathepsin D (CatD), in human monocyte-derived DCs. Inhibition of CatD specifically reduced the expansion of invariant NKT cells and furthermore resulted in decreased maturation of saposins, a group of lipid transfer proteins required for lysosomal lipid Ag processing and loading. These results reveal a novel mechanism of lipid Ag presentation and identify CatD as a key component of this machinery and firmly place PPARγ as the transcriptional regulator linking lipid metabolism and lipid Ag processing.
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