正常和营养不良小鼠肌生成调节因子的表达:IGF-1治疗的影响

H.H. Hsu, M.M. Zdanowicz , V.R. Agarwal , P.W. Speiser
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引用次数: 22

摘要

肌生成调节因子(MRFs)促进肌细胞从成纤维细胞分化,并由胰岛素样生长因子I (IGF-1)诱导。先前的研究表明,当用IGF-1治疗患有肌肉萎缩症的成熟小鼠时,新的肌肉蛋白的合成和肌肉形态的改善。我们研究了IGF-1的这些有益作用是否可能归因于磁磁共振成像的刺激。Maledy(129ReJ)小鼠和对照组(129J)在大约5周龄时被分配给IGF-1治疗(10 μg,每日两次)或不治疗,6周后处死。从骨骼肌中提取RNA,逆转录,并使用每个MRF特异性引物通过聚合酶链反应(PCR)扩增。采用竞争性PCR定量分析IGF-1处理后的myo表达。在对照组和小鼠肌肉中均检测到formyf-5、MRF4和myogenin的转录本;治疗组间无明显差异。转录本的定量分析表明,对照和鼠间没有显著的基础差异。然而,在IGF-1治疗后,实验组的myo表达明显升高,对照组的myo表达也有显著升高的趋势。这些数据表明IGF-1通过刺激mrf在胚胎后肌肉中发挥其体内效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of Myogenic Regulatory Factors in Normal and Dystrophic Mice: Effects of IGF-1 Treatment

Myogenic regulatory factors (MRFs) promote differentiation of muscle cells from fibroblasts and are induced by insulin-like growth factor I (IGF-1). Prior studies have shown synthesis of new muscle protein and improved muscle morphology when maturedymice with muscular dystrophy are treated with IGF-1. We investigated whether these salutary effects of IGF-1 might be attributable to stimulation of MRFs. Maledy(129ReJ) mice and controls (129J) were assigned to IGF-1 treatment (10 μg twice daily) or nontreatment at about 5 weeks of life and sacrificed 6 weeks later. RNA was extracted from skeletal muscles, reverse transcribed, and amplified by polymerase chain reaction (PCR) using primers specific for each MRF. Competitive PCR was performed to quantifyMyoDexpression in response to IGF-1 treatment. Transcripts formyf-5, MRF4,and myogenin were detected in both control anddymouse muscles; no apparent differences were observed between treatment groups. Quantitative analysis of transcripts forMyoDindicated no significant basal differences between control anddymice. There was, however, significantly higherMyoDexpression in thedygroup, and a trend toward significance in the control group, following IGF-1 treatment. These data suggest that IGF-1 exerts itsin vivoeffects in postembryonal muscle by stimulating MRFs.

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