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Calcineurin controls nerve activity-dependent specification of slow skeletal muscle fibers but not muscle growth

机译:钙调神经磷酸酶控制慢骨骼肌纤维的神经活动依赖性规格,但不控制肌肉生长

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摘要

Nerve activity can induce long-lasting, transcription-dependent changes in skeletal muscle fibers and thus affect muscle growth and fiber-type specificity. Calcineurin signaling has been implicated in the transcriptional regulation of slow muscle fiber genes in culture, but the functional role of calcineurin in vivo has not been unambiguously demonstrated. Here, we report that the up-regulation of slow myosin heavy chain (MyHC) and a MyHC-slow promoter induced by slow motor neurons in regenerating rat soleus muscle is prevented by the calcineurin inhibitors cyclosporin A (CsA), FK506, and the calcineurin inhibitory protein domain from cain/cabin-1. In contrast, calcineurin inhibitors do not block the increase in fiber size induced by nerve activity in regenerating muscle. The activation of MyHC-slow induced by direct electrostimulation of denervated regenerating muscle with a continuous low frequency impulse pattern is blocked by CsA, showing that calcineurin function in muscle fibers and not in motor neurons is responsible for nerve-dependent specification of slow muscle fibers. Calcineurin is also involved in the maintenance of the slow muscle fiber gene program because in the adult soleus muscle, cain causes a switch from MyHC-slow to fast-type MyHC-2X and MyHC-2B gene expression, and the activity of the MyHC-slow promoter is inhibited by CsA and FK506.
机译:神经活动可诱导骨骼肌纤维的持久,转录依赖性变化,从而影响肌肉生长和纤维类型特异性。钙调神经磷酸酶信号传导已参与培养中慢肌纤维基因的转录调控,但是钙调神经磷酸酶在体内的功能作用尚未得到明确证明。在这里,我们报道钙调神经磷酸酶抑制剂环孢菌素A(CsA),FK506和钙调神经磷酸酶阻止了慢肌球蛋白重链(MyHC)和慢运动神经元在大鼠比目鱼肌再生中诱导的MyHC慢启动子的上调。 cain / cabin-1的抑制蛋白结构域。相反,钙调神经磷酸酶抑制剂不会阻止再生肌肉中神经活动引起的纤维大小增加。 CsA抑制了由连续失活的低频脉冲模式对失神经的再生肌肉进行直接电刺激诱导的MyHC-slow的激活,这表明钙调神经磷酸酶在肌肉纤维中而不是在运动神经元中是慢肌纤维的神经依赖性指标。钙调神经磷酸酶也参与了慢肌纤维基因程序的维持,因为在成年比目鱼肌中,该隐会导致MyHC-low转换为MyHC-2X和MyHC-2B快速表达,以及M​​yHC-慢启动子被CsA和FK506抑制。

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