The Nuclear Receptor PPARs as Important Regulators of T-Cell Functions and Autoimmune Diseases

被引:175
作者
Choi, Je-Min [1 ,2 ]
Bothwell, Alfred L. M. [3 ]
机构
[1] Hanyang Univ, Res Inst Nat Sci, Dept Life Sci, Seoul 133791, South Korea
[2] Hanyang Univ, Hanyang Biomed Res Inst, Seoul 133791, South Korea
[3] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
关键词
autoimmune disease; nuclear receptor; PPAR; T cell; PROLIFERATOR-ACTIVATED-RECEPTOR; LIGAND-BINDING DOMAIN; GENE-EXPRESSION; GAMMA AGONISTS; TRANSCRIPTION FACTOR; FATTY-ACIDS; ALPHA; INFLAMMATION; INHIBIT; TRANSREPRESSION;
D O I
10.1007/s10059-012-2297-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Members of the nuclear receptor superfamily function as transcription factors involved in innate and adaptive immunity as well as lipid metabolism. These highly conserved proteins participate in ligand-dependent or -independent regulatory mechanisms that affect gene expression. Peroxisome proliferator-activated receptors (PPARs), which include PPAR alpha, PPAR beta/delta, and PPAR gamma, are a group of nuclear receptor proteins that play diverse roles in cellular differentiation, development, and metabolism. Each PPAR subfamily is activated by different endogenous and synthetic ligands. Recent studies using specific ligand treatments and cell type-specific PPAR knockout mice have revealed important roles for these proteins in T-cell-related autoimmune diseases. Moreover, PPARs have been shown to regulate T-cell survival, activation, and CD4(+) T helper cell differentiation into the Th1, Th2, Th17, and Treg lineages. Here, we review the studies that provide insight into the important regulatory roles of PPARs in T-cell activation, survival, proliferation, differentiation, and autoimmune disease.
引用
收藏
页码:217 / 222
页数:6
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