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Autoimmune Kidney Disease and Impaired Engulfment of Apoptotic Cells in Mice with Macrophage Peroxisome Proliferator-Activated Receptor γ or Retinoid X Receptor α Deficiency
Author(s) -
Tamás Rőszer,
María Piedad Menéndez-Gutiérrez,
Martina I. Lefterova,
Daniel Alameda,
Vanessa Núñez,
Mitchell A. Lazar,
T Fischer,
Mercedes Ricote
Publication year - 2010
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1002230
Subject(s) - lupus nephritis , autoimmunity , macrophage , retinoid x receptor , autoimmune disease , phagocytosis , glomerulonephritis , apoptosis , immunology , nuclear receptor , autoantibody , receptor , peroxisome proliferator activated receptor , biology , nephritis , endocrinology , medicine , kidney , immune system , disease , transcription factor , antibody , in vitro , biochemistry , gene
Autoimmune glomerulonephritis is a common manifestation of systemic lupus erythematosus (SLE). In this study, we show that mice lacking macrophage expression of the heterodimeric nuclear receptors PPARγ or RXRα develop glomerulonephritis and autoantibodies to nuclear Ags, resembling the nephritis seen in SLE. These mice show deficiencies in phagocytosis and clearance of apoptotic cells, and they are unable to acquire an anti-inflammatory phenotype upon feeding of apoptotic cells, which is critical for the maintenance of self-tolerance. These results demonstrate that stimulation of PPARγ and RXRα in macrophages facilitates apoptotic cell engulfment, and they provide a potential strategy to avoid autoimmunity against dying cells and to attenuate SLE.

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