Down-regulation of lipoprotein lipase increases glucose uptake in L6 muscle cells

被引:6
|
作者
Lopez, Veronica [1 ]
Saraff, Kumuda [1 ]
Medh, Jheem D. [1 ]
机构
[1] Calif State Univ Northridge, Dept Chem & Biochem, Northridge, CA 91330 USA
基金
美国国家卫生研究院;
关键词
PPAR-gamma; Ciglitazone; Lipoprotein lipase; Skeletal muscle; Rat L6 cells; Glucose uptake; siRNA; ACTIVATED RECEPTOR-GAMMA; INSULIN-RESISTANCE; PPAR-GAMMA; OVEREXPRESSION; TROGLITAZONE; METABOLISM; GENE;
D O I
10.1016/j.bbrc.2009.08.081
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
Thiazolidinediones (TZDs) are synthetic hypoglycemic agents used to treat type 2 diabetes. TZDs target the peroxisome proliferator activated receptor-gamma (PPAR-gamma) and improve systemic insulin sensitivity. The contributions of specific tissues to TZD action, or the downstream effects of PPAR-gamma activation, are not very clear. We have used a rat skeletal muscle cell line (L6 cells) to demonstrate that TZDs directly target PPAR-gamma in muscle cells. TZD treatment resulted in a significant repression of lipoprotein lipase (LPL) expression in L6 cells. This repression correlated with an increase in glucose uptake. Down-regulation of LPL message and protein levels using siRNA resulted in a similar increase in insulin-dependent glucose uptake. Thus, LPL down-regulation improved insulin sensitivity independent of TZDs. This finding provides a novel method for the management of insulin resistance. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 39
页数:6
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