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Regeneration of Transgenic Skeletal Muscles with Altered Timing of Expression of the Basic Helix-Loop-Helix Muscle Regulatory Factor MRF4

机译:基本的螺旋-循环-螺旋肌肉调节因子MRF4表达的改变时间的转基因骨骼肌的再生。

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摘要

In regenerating muscle cells, muscle regulatory factor (MRF) 4 is normally the last of the four MRFs to be expressed. To analyze how the timing of MRF4 expression affects muscle regeneration, we compared regeneration after local freeze injury of muscles from wild-type mice with muscles from transgenic mice in which MRF4 expression was under control of an ∼1.6-kb fragment of the myogenin promoter. Three days after injury, masseter and tibialis anterior (TA) muscles in wild-type mice expressed little or no MRF4 mRNA; whereas these muscles in transgenic mice expressed abundant MRF4 mRNA from both the transgene and the endogenous gene. Thus, MRF4 up-regulation was accelerated in transgenic compared to wild-type regenerating muscles, and expression of the transgene appeared to activate, perhaps indirectly, expression of the endogenous MRF4 gene. At 11 days after injury, regeneration, as measured by cross-sectional area and density of regenerated fibers, was significantly impaired in transgenic TA compared to wild-type TA, whereas at 19 days after injury both transgenic and TA muscle fibers had fully recovered to preinjury values. Regeneration of masseter muscles, which normally regenerate much less completely than TA muscles, was unaffected by the transgene. Thus, the timing of MRF4 up-regulation, as well as additional muscle-specific factors, can determine the progress of muscle regeneration.
机译:在再生肌肉细胞中,肌肉调节因子(MRF)4通常是要表达的四个MRF中的最后一个。为了分析MRF4表达的时机如何影响肌肉再生,我们比较了野生型小鼠肌肉局部冻伤后与MRF4表达受肌原蛋白启动子约1.6kb片段控制的转基因小鼠肌肉再生后的再生。受伤三天后,野生型小鼠的咬肌和胫前肌(TA)很少表达或不表达MRF4 mRNA。而转基因小鼠中的这些肌肉表达了来自转基因和内源基因的大量MRF4 mRNA。因此,与野生型再生肌肉相比,转基因中的MRF4上调被加速了,转基因的表达似乎可以间接激活内源性MRF4基因的表达。与野生型TA相比,在损伤后11天,通过横截面积和再生纤维的密度衡量,再生显着削弱了转基因TA的再生,而在损伤后19天,转基因和TA肌肉纤维均已完全恢复至损伤前的价值观。咬肌的再生通常不受TA肌肉的影响要少得多,但不受转基因的影响。因此,MRF4上调的时机以及其他特定于肌肉的因素可以确定肌肉再生的进程。

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