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Regulation of lipid droplet size and phospholipid composition by stearoyl-CoA desaturase

机译:硬脂酰辅酶A去饱和酶调节脂滴大小和磷脂组成

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摘要

Fatty acid desaturation regulates membrane function and fat storage in animals. To determine the contribution of stearoyl-CoA desaturase (SCD) activity on fat storage and development in the nematode Caenorhabditis elegans, we analyzed the lipid composition and lipid droplet size in the fat-6;fat-7 desaturase mutants independently and in combination with mutants disrupted in conserved lipid metabolic pathways. C. elegans with impaired SCD activity displayed both reduced fat stores and decreased lipid droplet size. Mutants in the daf-2 (insulin-like growth factor receptor), rsks-1 (homolog of p70S6kinase, an effector of the target of rapamycin signaling pathway), and daf-7 (transforming growth factor β) displayed high fat stores, the opposite of the low fat observed in the fat-6;fat-7 desaturase mutants. The metabolic mutants in combination with fat-6;fat-7 displayed low fat stores, with the exception of the daf-2;fat-6;fat-7 triple mutants, which had increased de novo fatty acid synthesis and wild-type levels of fat stores. Notably, SCD activity is required for the formation of large-sized lipid droplets in all mutant backgrounds, as well as for normal ratios of phosphatidylcholine (PC) to phosphatidylethanolamine (PE). These studies reveal previously uncharacterized roles for SCD in the regulation of lipid droplet size and membrane phospholipid composition.
机译:脂肪酸去饱和调节动物的膜功能和脂肪储存。为了确定硬脂酰辅酶A去饱和酶(SCD)活性对线虫秀丽隐杆线虫中脂肪存储和发育的贡献,我们独立地和结合突变体分析了fat-6; fat-7去饱和酶突变体中的脂质组成和脂质滴大小。破坏了保守的脂质代谢途径。 SCD活性受损的秀丽隐杆线虫显示出减少的脂肪储存和减少的脂质滴大小。 daf-2(胰岛素样生长因子受体),rsks-1(p70S6激酶的同源物,雷帕霉素信号传导途径的靶标的效应子)和daf-7(转化生长因子β)中的突变体显示出高脂肪储存,与在fat-6; fat-7去饱和酶突变体中观察到的低脂肪相反。与daf-2; fat-6; fat-7三重突变体结合的代谢突变体与fat-6; fat-7组合显示出较低的脂肪储存,其增加了从头脂肪酸合成和野生型水平脂肪商店。值得注意的是,SCD活性是在所有突变体背景中形成大型脂质液滴以及磷脂酰胆碱(PC)与磷脂酰乙醇胺(PE)的正常比例所必需的。这些研究揭示了SCD以前在脂质滴大小和膜磷脂组成的调节中所没有的作用。

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