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首页> 外文期刊>The British Journal of Nutrition >Low-molecular-weight fucoidan regulates myogenic differentiation through the mitogen-activated protein kinase pathway in C2C12 cells.
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Low-molecular-weight fucoidan regulates myogenic differentiation through the mitogen-activated protein kinase pathway in C2C12 cells.

机译:低分子量岩藻依聚糖通过C2C12细胞中的有丝分裂原激活的蛋白激酶途径调节肌原性分化。

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摘要

Low-molecular-weight fucoidan (LMWF) has been broadly studied in recent years due to its numerous biological properties. Nevertheless, there have been no reports about the effects of LMWF on myogenic differentiation (MyoD). The objective of the present study was to demonstrate the impact of LMWF on myogenesis in C2C12 cells. The ultimate aim was to establish whether LMWF regulates myogenesis similar to heparin as a partial regulator of myogenesis. LMWF was prepared at a minimal size by ultra-filtration compared with crude fucoidan. We treated C2C12 cells with LMWF and/or heparin during MyoD. The data from the present study are the first to suggest that LMWF suppresses the expression of the myogenic regulatory factors and the myocyte enhancer factors as well as the morphological changes that occur during differentiation. Additionally, the expression of the mitogen-activated protein kinase (MAPK) family was significantly inhibited by LMWF when compared with controls. The LMWF-treated group showed significantly decreased expression of reactive oxygen species (ROS) enzymes compared with control cells. Heparin was used as a positive control because it has been reported to activate MyoD. Taken together, these results suggest that LMWF might regulate MyoD through the MAPK pathway and by regulating ROS activity in C2C12 cells
机译:低分子量岩藻依聚糖(LMWF)由于其众多的生物学特性,近年来已得到广泛研究。然而,还没有关于LMWF对肌原性分化(MyoD)的影响的报道。本研究的目的是证明LMWF对C2C12细胞肌发生的影响。最终目的是确定LMWF是否像肝素一样调节肌生成,作为肝生成的部分调节剂。与粗品岩藻依聚糖相比,LMWF是通过超滤以最小尺寸制备的。在MyoD期间,我们用LMWF和/或肝素处理了C2C12细胞。来自本研究的数据首次表明LMWF抑制了肌源性调节因子和肌细胞增强因子的表达以及分化过程中发生的形态变化。此外,与对照组相比,LMWF显着抑制了促分裂原活化蛋白激酶(MAPK)家族的表达。与对照组相比,LMWF治疗组的活性氧(ROS)酶表达明显降低。肝素被用作阳性对照,因为据报道它可以激活MyoD。综上所述,这些结果表明LMWF可能通过MAPK途径和通过调节C2C12细胞中的ROS活性来调节MyoD。

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