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首页> 外文期刊>Genes to cells : >Critical role of Frizzled1 in age-related alterations of Wnt/beta-catenin signal in myogenic cells during differentiation
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Critical role of Frizzled1 in age-related alterations of Wnt/beta-catenin signal in myogenic cells during differentiation

机译:Frizzled1在分化过程中成年细胞中Wnt /β-catenin信号的年龄相关变化中的关键作用

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Activation of Wnt/beta-catenin signal in muscle satellite cells (mSCs) of aged mice during myogenic differentiation has been appreciated as an important age-related feature of the skeletal muscles, resulting in impairment of their regenerative ability following muscle injury. However, it remains elusive about molecules involved in this age-related alteration of Wnt/beta-catenin signal in myogenic cells. To clarify this issue, we carried out expression analyses of Wnt receptor genes using real-time RT-PCR in mSCs isolated from the skeletal muscles of young and aged mice. Here, we show that expression of Frizzled1 (Fzd1) was detected at high levels in mSCs of aged mice. Higher expression levels of Fzd1 were also detected in mSC-derived myogenic cells from aged mice and associated with activation of Wnt/beta-catenin signal during their myogenic differentiation in vitro. We also provide evidence that suppressed expression of Fzd1 in myogenic cells from aged mice results in a significant increase in myogenic differentiation, and its forced expression in those from young mice results in its drastic inhibition. These findings indicate the critical role of Fzd1 in altered myogenic differentiation associated with aging.
机译:Wnt /β-catenin信号在成肌分化过程中在衰老小鼠的肌肉卫星细胞(mSCs)中的激活已被认为是骨骼肌与年龄相关的重要特征,导致肌肉损伤后其再生能力受损。然而,仍然不清楚在成肌细胞中这种与年龄有关的Wnt /β-catenin信号改变的分子。为了阐明这个问题,我们使用实时RT-PCR在从幼年和老年小鼠骨骼肌分离的mSC中进行了Wnt受体基因的表达分析。在这里,我们显示在高龄小鼠的mSC中高水平检测到Frizzled1(Fzd1)的表达。在老年小鼠的mSC来源的成肌细胞中也检测到较高的Fzd1表达水平,并且与Wnt /β-catenin信号在其成肌分化过程中的激活有关。我们还提供了证据,表明Fzd1在衰老小鼠的成肌细胞中的表达受到抑制,导致成肌分化显着增加,而在年轻小鼠的肌成纤维细胞中被强迫表达导致其强烈抑制。这些发现表明Fzd1在与衰老相关的成肌分化改变中起关键作用。

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