首页> 外文OA文献 >Investigation of the Expression of Myogenic Transcription Factors, microRNAs and Muscle-Specific E3 Ubiquitin Ligases in the Medial Gastrocnemius and Soleus Muscles following Peripheral Nerve Injury
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Investigation of the Expression of Myogenic Transcription Factors, microRNAs and Muscle-Specific E3 Ubiquitin Ligases in the Medial Gastrocnemius and Soleus Muscles following Peripheral Nerve Injury

机译:周围神经损伤后内侧腓肠肌和比目鱼肌中成肌转录因子,microRNA和特定于肌肉的E3泛素中的表达的调查

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摘要

Despite surgical innovation, the sensory and motor outcome after a peripheral nerve injury remains incomplete. One contributing factor to the poor outcome is prolonged denervation of the target organ, leading to apoptosis of both mature myofibres and satellite cells with subsequent replacement of the muscle tissue with fibrotic scar and adipose tissue. In this study, we investigated the expression of myogenic transcription factors, muscle specific microRNAs and muscle-specific E3 ubiquitin ligases at several time points following denervation in two different muscles, the gastrocnemius (containing predominantly fast type fibres) and soleus (slow type) muscles, since these molecules may influence the degree of atrophy following denervation. Both muscles exhibited significant atrophy (compared with the contra-lateral sides) at 7 days following either a nerve transection or crush injury. In the crush model, the soleus muscle showed significantly increased muscle weights at days 14 and 28 which was not the case for the gastrocnemius muscle which continued to atrophy. There was a significantly more pronounced up-regulation of MyoD expression in the denervated soleus muscle compared with the gastrocnemius muscle. Conversely, myogenin was more markedly elevated in the gastrocnemius versus soleus muscles. The muscles also showed significantly contrasting transcriptional regulation of the microRNAs miR-1 and miR-206. MuRF1 and Atrogin-1 showed the highest levels of expression in the denervated gastrocnemius muscle. This study provides further insights regarding the intracellular regulatory molecules that generate and maintain distinct patterns of gene expression in different fibre types following peripheral nerve injury.
机译:尽管进行了外科手术创新,但周围神经损伤后的感觉和运动结果仍不完全。不良结果的一个促成因素是靶器官的长期失神经,导致成熟的肌纤维和卫星细胞的凋亡,随后用纤维化疤痕和脂肪组织代替肌肉组织。在这项研究中,我们研究了腓肠肌(主要包含快速型纤维)和比目鱼(慢型)肌肉去神经支配后几个时间点的肌转录因子,肌肉特异性microRNA和肌肉特异性E3泛素连接酶的表达。 ,因为这些分子可能会影响去神经后萎缩的程度。在神经横断或挤压伤后7天,两条肌肉均表现出明显的萎缩(与对侧相比)。在挤压模型中,比目鱼肌在第14天和第28天显示出明显的肌肉重量增加,而腓肠肌继续萎缩则不是这种情况。与腓肠肌相比,失神经的比目鱼肌中MyoD表达明显上调。相反,腓肠肌与比目鱼肌相比肌生成素明显升高。肌肉还显示出microRNA miR-1和miR-206的转录调控形成明显对比。 MuRF1和Atrogin-1在失神经的腓肠肌中显示出最高水平的表达。这项研究提供有关在周围神经损伤后在不同纤维类型中产生并维持不同基因表达模式的细胞内调节分子的进一步见解。

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