期刊
PLOS ONE
卷 9, 期 6, 页码 -出版社
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0099127
关键词
-
资金
- Basic Science Research Program through National Research Foundation of Korea [NRF-2011-0012859, NRF-2013R1A1A2A10060048]
- NIH [HL088258, AR40072]
Peroxisome proliferator-activated receptor gamma (PPAR gamma) is a transcription factor that regulates lipid and glucose metabolism. Although studies of PPAR gamma ligands have demonstrated its regulatory functions in inflammation and adaptive immunity, its intrinsic role in T cells and autoimmunity has yet to be fully elucidated. Here we used CD4-PPAR gamma(KO) mice to investigate PPAR gamma-deficient T cells, which were hyper-reactive to produce higher levels of cytokines and exhibited greater proliferation than wild type T cells with increased ERK and AKT phosphorylation. Diminished expression of I kappa B alpha, Sirt1, and Foxo1, which are inhibitors of NF-kappa B, was observed in PPAR gamma-deficient T cells that were prone to produce all the signature cytokines under Th1, Th2, Th17, and Th9 skewing condition. Interestingly, 1-year-old CD4-PPAR gamma(KO) mice spontaneously developed moderate autoimmune phenotype by increased activated T cells, follicular helper T cells (T-FH cells) and germinal center B cells with glomerular inflammation and enhanced autoantibody production. Sheep red blood cell immunization more induced T-FH cells and germinal centers in CD4-PPAR gamma(KO) mice and the T cells showed increased of Bcl-6 and IL-21 expression suggesting its regulatory role in germinal center reaction. Collectively, these results suggest that PPAR gamma has a regulatory role for T-FH cells and germinal center reaction to prevent autoimmunity.
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