Fraher Daniel, Ellis Megan K, Morrison Shona, McGee Sean L, Ward Alister C, Walder Ken, Gibert Yann
Metabolic Research Unit, Deakin University School of Medicine, Geelong 3217, Australia.
Endocrinology. 2015 Oct;156(10):3596-609. doi: 10.1210/EN.2015-1315. Epub 2015 Jul 16.
The endocannabinoid system (ECS) and retinoic acid (RA) signaling have been associated with influencing lipid metabolism. We hypothesized that modulation of these pathways could modify lipid abundance in developing vertebrates and that these pathways could have a combinatorial effect on lipid levels. Zebrafish embryos were exposed to chemical treatments altering the activity of the ECS and RA pathway. Embryos were stained with the neutral lipid dye Oil-Red-O (ORO) and underwent whole-mount in situ hybridization (WISH). Mouse 3T3-L1 fibroblasts were differentiated under exposure to RA-modulating chemicals and subsequently stained with ORO and analyzed for gene expression by qRT-PCR. ECS activation and RA exposure increased lipid abundance and the expression of lipoprotein lipase. In addition, RA treatment increased expression of CCAAT/enhancer-binding protein alpha. Both ECS receptors and RA receptor subtypes were separately involved in modulating lipid abundance. Finally, increased ECS or RA activity ameliorated the reduced lipid abundance caused by peroxisome proliferator-activated receptor gamma (PPARγ) inhibition. Therefore, the ECS and RA pathway influence lipid abundance in zebrafish embryos and have an additive effect when treated simultaneously. Furthermore, we demonstrated that these pathways act downstream or independently of PPARγ to influence lipid levels. Our study shows for the first time that the RA and ECS pathways have additive function in lipid abundance during vertebrate development.
内源性大麻素系统(ECS)和视黄酸(RA)信号传导与影响脂质代谢有关。我们假设调节这些途径可以改变发育中的脊椎动物的脂质丰度,并且这些途径可能对脂质水平产生联合作用。斑马鱼胚胎接受化学处理以改变ECS和RA途径的活性。胚胎用中性脂质染料油红O(ORO)染色,并进行全胚胎原位杂交(WISH)。小鼠3T3-L1成纤维细胞在暴露于RA调节化学物质的条件下分化,随后用ORO染色,并通过qRT-PCR分析基因表达。ECS激活和RA暴露增加了脂质丰度和脂蛋白脂肪酶的表达。此外,RA处理增加了CCAAT/增强子结合蛋白α的表达。ECS受体和RA受体亚型均分别参与调节脂质丰度。最后,增加ECS或RA活性改善了由过氧化物酶体增殖物激活受体γ(PPARγ)抑制引起的脂质丰度降低。因此,ECS和RA途径影响斑马鱼胚胎中的脂质丰度,并且在同时处理时具有累加效应。此外,我们证明这些途径在PPARγ的下游起作用或独立于PPARγ来影响脂质水平。我们的研究首次表明,RA和ECS途径在脊椎动物发育过程中对脂质丰度具有累加功能。