Institute for Molecular Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Immunol Rev. 2012 Sep;249(1):72-83. doi: 10.1111/j.1600-065X.2012.01153.x.
Lipid metabolism has emerged as an important modulator of innate and adaptive immune cell fate and function. The lipid-activated transcription factors peroxisome proliferator-activated receptor (PPAR) α, β/δ, γ and liver X receptor (LXR) are members of the nuclear receptor superfamily that have a well-defined role in regulating lipid homeostasis and metabolic diseases. Accumulated evidence over the last decade indicates that PPAR and LXR signaling also influence multiple facets of inflammation and immunity, thereby providing important crosstalk between metabolism and immune system. Herein, we provide a brief introduction to LXR and PPAR biology and review recent discoveries highlighting the importance of PPAR and LXR signaling in the modulation of normal and pathologic states of immunity. We also examine advances in our mechanistic understanding of how nuclear receptors impact immune system function and homeostasis. Finally, we discuss whether LXRs and PPARs could be pharmacologically manipulated to provide novel therapeutic approaches for modulation of the immune system under pathologic inflammation or in the context of allergic and autoimmune disease.
脂代谢已成为先天和适应性免疫细胞命运和功能的重要调节因子。脂激活转录因子过氧化物酶体增殖物激活受体 (PPAR)α、β/δ、γ 和肝 X 受体 (LXR) 是核受体超家族的成员,它们在调节脂质稳态和代谢疾病方面具有明确的作用。过去十年的积累证据表明,PPAR 和 LXR 信号也会影响炎症和免疫的多个方面,从而为代谢和免疫系统之间提供重要的串扰。本文简要介绍了 LXR 和 PPAR 的生物学,并回顾了最近的发现,强调了 PPAR 和 LXR 信号在调节免疫正常和病理状态中的重要性。我们还研究了我们对核受体如何影响免疫系统功能和稳态的机制理解的进展。最后,我们讨论了 LXR 和 PPAR 是否可以通过药理学手段进行操纵,以提供在病理炎症或过敏和自身免疫性疾病背景下调节免疫系统的新的治疗方法。