Schmidt Simone, Willers Janina, Riecker Sabine, Möller Katharina, Schuchardt Jan Philipp, Hahn Andreas
Institute of Food Science and Human Nutrition, Leibniz University of Hannover, Am Kleinen Felde 30, 30167, Hannover, Germany.
Lipids Health Dis. 2015 Feb 14;14:4. doi: 10.1186/1476-511X-14-4.
Omega-3 polyunsaturated fatty acids (n-3 PUFAs) show beneficial effects on cardiovascular health and cognitive functions, but the underlying molecular mechanisms are not completely understood. Because of the fact that cytoskeleton dynamics affect almost every cellular process, the regulation of cytoskeletal dynamics could be a new pathway by which n-3 PUFAs exert their effects on cellular level.
A 12-week open-label intervention study with 12 healthy men was conducted to determine the effects of 2.7 g/d n-3 PUFA on changes in mRNA expression of cytoskeleton-associated genes by quantitative real-time PCR in whole blood. Furthermore, the actin content in red blood cells was analyzed by immunofluorescence imaging.
N-3 PUFA supplementation resulted in a significant down-regulation of cytoskeleton-associated genes, in particular three GTPases (RAC1, RHOA, CDC42), three kinases (ROCK1, PAK2, LIMK), two Wiskott-Aldrich syndrome proteins (WASL, WASF2) as well as actin related protein 2/3 complex (ARPC2, ARPC3) and cofilin (CFL1). Variability in F-actin content between subjects was high; reduced actin content was only reduced within group evaluation.
Reduced cytoskeleton-associated gene expression after n-3 PUFA supplementation suggests that regulation of cytoskeleton dynamics might be an additional way by which n-3 PUFAs exert their cellular effects. Concerning F-actin, this analysis did not reveal unmistakable results impeding a generalized conclusion.
ω-3多不饱和脂肪酸(n-3 PUFAs)对心血管健康和认知功能具有有益作用,但其潜在的分子机制尚未完全明确。由于细胞骨架动力学几乎影响每个细胞过程,因此细胞骨架动力学的调节可能是n-3 PUFAs在细胞水平发挥作用的新途径。
对12名健康男性进行了一项为期12周的开放标签干预研究,以通过全血定量实时PCR确定每天2.7 g n-3 PUFA对细胞骨架相关基因mRNA表达变化的影响。此外,通过免疫荧光成像分析红细胞中的肌动蛋白含量。
补充n-3 PUFA导致细胞骨架相关基因显著下调,特别是三种GTP酶(RAC1、RHOA、CDC42)、三种激酶(ROCK1、PAK2、LIMK)、两种威斯科特-奥尔德里奇综合征蛋白(WASL、WASF2)以及肌动蛋白相关蛋白2/3复合物(ARPC2、ARPC3)和丝切蛋白(CFL1)。受试者之间F-肌动蛋白含量的变异性很高;仅在组内评估中肌动蛋白含量降低。
补充n-3 PUFA后细胞骨架相关基因表达降低表明,细胞骨架动力学的调节可能是n-3 PUFAs发挥细胞作用的另一种方式。关于F-肌动蛋白,该分析未得出明确结果,无法得出一般性结论。