过氧化物酶体增殖物激活受体
核受体
脂肪生成
免疫系统
受体
转录因子
过氧化物酶体增殖物激活受体δ
细胞生物学
能量稳态
过氧化物酶体增殖物激活受体γ
脂质代谢
脂肪组织
过氧化物酶体
葡萄糖稳态
生物
内分泌学
免疫学
生物化学
胰岛素抵抗
胰岛素
基因
作者
Anthos Christofides,Eirini Konstantinidou,Chinmay Jani,Vassiliki A. Boussiotis
标识
DOI:10.1016/j.metabol.2020.154338
摘要
Peroxisome proliferator-activated receptors (PPARs) are fatty acid-activated transcription factors of nuclear hormone receptor superfamily that regulate energy metabolism. Currently, three PPAR subtypes have been identified: PPARα, PPARγ, and PPARβ/δ. PPARα and PPARδ are highly expressed in oxidative tissues and regulate genes involved in substrate delivery and oxidative phosphorylation (OXPHOS) and regulation of energy homeostasis. In contrast, PPARγ is more important in lipogenesis and lipid synthesis, with highest expression levels in white adipose tissue (WAT). In addition to tissues regulating whole body energy homeostasis, PPARs are expressed in immune cells and have an emerging critical role in immune cell differentiation and fate commitment. In this review, we discuss the actions of PPARs in the function of the innate and the adaptive immune system and their implications in immune-mediated inflammatory conditions.
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