Knockdown of pyruvate carboxylase or fatty acid synthase lowers numerous lipids and glucose-stimulated insulin release in insulinoma cells

被引:7
作者
MacDonald, Michael J. [1 ]
Hasan, Noaman M. [1 ]
Dobrzyn, Agnieszka [2 ]
Stoker, Scott W. [1 ]
Ntambi, James M. [3 ,4 ]
Liu, Xueqing [3 ,4 ]
Sampath, Harini [3 ,4 ,5 ]
机构
[1] Univ Wisconsin, Childrens Diabet Ctr, Sch Med & Publ Hlth, Madison, WI 53706 USA
[2] M Nencki Inst Expt Biol, Lab Cell Signaling & Metab Disorders, PL-02093 Warsaw, Poland
[3] Univ Wisconsin, Coll Agr & Life Sci, Dept Biochem, Madison, WI 53706 USA
[4] Univ Wisconsin, Coll Agr & Life Sci, Dept Nutr Sci, Madison, WI 53706 USA
[5] Oregon Hlth & Sci Univ, Ctr Study Weight Regulat, Portland, OR 97201 USA
关键词
Insulinoma cells; shRNA; Pyruvate carboxylase; Fatty acid synthase; Phospholipids; Cholesterol esters; Lipid remodeling; ATP-CITRATE-LYASE; MOUSE PANCREATIC-ISLETS; INS-1; CELLS; BETA-CELLS; REGULATED ANAPLEROSIS; OBESE MICE; SECRETION; METABOLISM; ACETOACETATE; ENZYME;
D O I
10.1016/j.abb.2013.01.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We previously showed that knockdown of the anaplerotic enzyme pyruvate carboxylase in the INS-1 832/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 C-14-C-24 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. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 31
页数:9
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