Briolay Anne, Jaafar Rami, Nemoz Georges, Bessueille Laurence
Université Lyon 1, CNRS, UMR 5246, Institut de Chimie et Biochimie Moléculaires et Supramoléculaires, IMBL, F-69622 Villeurbanne, France.
Biochim Biophys Acta. 2013 Feb;1828(2):602-13. doi: 10.1016/j.bbamem.2012.10.006. Epub 2012 Oct 16.
Lipid composition and fatty acid analysis of the major classes of membrane phospholipids were determined during myogenic differentiation of L6 skeletal muscle cells. The cholesterol to glycerophospholipids ratio decreased during differentiation, both in total (TM) and detergent-resistant membranes (DRM). Analyses of the membrane lipids showed that differentiation had a major impact on the molecular composition of glycerophospholipids. A significant decrease in the concentration of saturated fatty acids was detected in glycerophospholipid classes, and to a lesser extent in sphingolipids, while the concentration of 16:1n-7, 18:1n-7 and 18:1n-9 increased. At the same time, the concentration of long polyunsaturated fatty acid chains decreased in TM and DRM glycerophospholipids, resulting in a lower saturated to unsaturated fatty acid ratio in myotubes as compared to myoblasts. Interestingly, the observed n-3/n-6 ratio was lower in differentiated cell membranes. PUFA supplementation of L6 cells led to an increase in myogenic differentiation correlated to an incorporation of added PUFAs in TM and DRM glycerophospholipids. As expected after n-3 PUFA supplementation, the n-3/n-6 ratio was clearly increased in TM and, surprisingly, this was also the case in isolated DRM. n-3 and n-6 PUFAs significantly and time-dependently increased the phosphorylation of kinase p70S6K1 during myogenic differentiation, revealing the activation of the upstream kinase mTORC1, a major regulator of cell cycle and protein translation. In contrast, PUFAs did not affect the phosphorylation of the kinase Akt, another pivotal regulator of cell metabolism. These results suggest that PUFA supplementation modified the membrane lipid composition and affected the differentiation of L6 cells.
在L6骨骼肌细胞的成肌分化过程中,对主要类别的膜磷脂进行了脂质组成和脂肪酸分析。在分化过程中,总膜(TM)和抗去污剂膜(DRM)中的胆固醇与甘油磷脂比率均下降。膜脂质分析表明,分化对甘油磷脂的分子组成有重大影响。在甘油磷脂类别中检测到饱和脂肪酸浓度显著降低,在鞘脂中降低程度较小,而16:1n - 7、18:1n - 7和18:1n - 9的浓度增加。同时,TM和DRM甘油磷脂中长链多不饱和脂肪酸链的浓度降低,导致与成肌细胞相比,肌管中饱和脂肪酸与不饱和脂肪酸的比率更低。有趣的是,在分化的细胞膜中观察到的n - 3/n - 6比率较低。用多不饱和脂肪酸(PUFA)补充L6细胞导致成肌分化增加,这与添加的PUFA掺入TM和DRM甘油磷脂有关。正如补充n - 3 PUFA后预期的那样,TM中的n - 3/n - 6比率明显增加,令人惊讶的是,分离的DRM中也是如此。在成肌分化过程中,n - 3和n - 6 PUFAs显著且随时间依赖性地增加激酶p70S6K1的磷酸化,揭示了上游激酶mTORC1的激活,mTORC1是细胞周期和蛋白质翻译的主要调节因子。相比之下,PUFAs不影响激酶Akt的磷酸化,Akt是细胞代谢的另一个关键调节因子。这些结果表明,补充PUFA改变了膜脂质组成并影响了L6细胞的分化。