Childrens Diabetes Center, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA.
Arch Biochem Biophys. 2013 Apr 1;532(1):23-31. doi: 10.1016/j.abb.2013.01.002. Epub 2013 Jan 25.
We previously showed that knockdown of the anaplerotic enzyme pyruvate carboxylase in the INS-1 832/13 insulinoma cell line inhibited glucose-stimulated insulin release and glucose carbon incorporation into lipids. We now show that knockdown of fatty acid synthase (FAS) mRNA and protein also inhibits glucose-stimulated insulin release in this cell line. Levels of numerous phospholipids, cholesterol esters, diacylglycerol, triglycerides and individual fatty acids with C14-C24 side chains were acutely lowered about 20% in glucose-stimulated pyruvate carboxylase knockdown cells over a time course that coincides with insulin secretion. In FAS knockdown cells glucose carbon incorporation into lipids and the levels of the subclasses of phospholipids and cholesterol ester species were lower by 20-30% without inhibition of glucose oxidation. These studies suggest that rapid lipid modification is essential for normal glucose-stimulated insulin secretion.
我们之前的研究表明,敲低 INS-1 832/13 胰岛素瘤细胞系中的氨甲酰磷酸合成酶可抑制葡萄糖刺激的胰岛素释放和葡萄糖碳掺入脂质。我们现在表明,脂肪酸合酶 (FAS) mRNA 和蛋白的敲低也会抑制该细胞系中葡萄糖刺激的胰岛素释放。在葡萄糖刺激的丙酮酸羧化酶敲低细胞中,在与胰岛素分泌一致的时间过程中,许多磷脂、胆固醇酯、二酰基甘油、甘油三酯和具有 C14-C24 侧链的单个脂肪酸的水平急剧降低约 20%。在 FAS 敲低细胞中,葡萄糖碳掺入脂质以及磷脂和胆固醇酯种类的亚类水平降低了 20-30%,而葡萄糖氧化没有受到抑制。这些研究表明,快速的脂质修饰对于正常的葡萄糖刺激的胰岛素分泌是必不可少的。