Keller H, Mahfoudi A, Dreyer C, Hihi A K, Medin J, Ozato K, Wahli W
Institut de Biologie animale, Université de Lausanne, Switzerland.
Ann N Y Acad Sci. 1993 Jun 11;684:157-73. doi: 10.1111/j.1749-6632.1993.tb32279.x.
PPARs are nuclear hormone receptors which, like the retinoid, thyroid hormone, vitamin D, and steroid hormone receptors, are ligand-activated transcription factors mediating the hormonal control of gene expression. Two lines of evidence indicate that PPARs have an important function in fatty acid metabolism. First, PPARs are activated by hypolipidemic drugs and physiological concentrations of fatty acids, and second, PPARs control the peroxisomal beta-oxidation pathway of fatty acids through transcriptional induction of the gene encoding the acyl-CoA oxidase (ACO), which is the rate-limiting enzyme of the pathway. Furthermore, the PPAR signaling pathway appears to converge with the 9-cis retinoic acid receptor (RXR) signaling pathway in the regulation of the ACO gene because heterodimerization between PPAR and RXR is essential for in vitro binding to the PPRE and because the strongest stimulation of this gene is observed when both receptors are exposed simultaneously to their activators. Thus, it appears that PPARs are involved in the 9-cis retinoic acid signaling pathway and that they play a pivotal role in the hormonal control of lipid metabolism.
过氧化物酶体增殖物激活受体(PPARs)是核激素受体,与视黄酸、甲状腺激素、维生素D和类固醇激素受体一样,是配体激活的转录因子,介导基因表达的激素调控。有两方面证据表明PPARs在脂肪酸代谢中具有重要功能。第一,PPARs可被降血脂药物和生理浓度的脂肪酸激活;第二,PPARs通过转录诱导编码酰基辅酶A氧化酶(ACO)的基因来控制脂肪酸的过氧化物酶体β-氧化途径,ACO是该途径的限速酶。此外,在酰基辅酶A氧化酶基因的调控中,PPAR信号通路似乎与9-顺式视黄酸受体(RXR)信号通路汇聚,因为PPAR与RXR之间的异二聚化对于体外结合过氧化物酶体增殖物反应元件(PPRE)至关重要,而且当两种受体同时暴露于其激活剂时,该基因受到的刺激最强。因此,似乎PPARs参与了9-顺式视黄酸信号通路,并且在脂质代谢的激素调控中起关键作用。