Departamento de Cardiología Regenerativa, Centro Nacional de Investigaciones Cardiovasculares, 28029 Madrid, Spain.
J Immunol. 2011 Jan 1;186(1):621-31. doi: 10.4049/jimmunol.1002230. Epub 2010 Dec 6.
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.
自身免疫性肾小球肾炎是系统性红斑狼疮(SLE)的常见表现。在这项研究中,我们表明,缺乏巨噬细胞表达的异二聚体核受体 PPARγ 或 RXRα 的小鼠会发展为肾小球肾炎和针对核抗原的自身抗体,类似于 SLE 中所见的肾炎。这些小鼠表现出吞噬和清除凋亡细胞的缺陷,并且在用凋亡细胞喂养时无法获得抗炎表型,这对于维持自身耐受至关重要。这些结果表明,巨噬细胞中 PPARγ 和 RXRα 的刺激促进了凋亡细胞的吞噬作用,为避免针对死亡细胞的自身免疫和减轻 SLE 提供了一种潜在策略。