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Biomechanical effects on microRNA expression in skeletal muscle differentiation

机译:对骨骼肌分化中微小RNA表达的生物力学作用

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We examined whether mechanical stretch affected expression of muscle-specific microRNAs (miRNAs) that regulate proliferation (miR-133a) or differentiation (miR-1, -206). Real-time quantitative RT-PCR was used to assess miRNA regulation in the murine myoblast cell line C2C12 exposed to stretch regimens that promote either proliferation (high stretch: 17%, 1 Hz) or differentiation (moderate stretch: 10%, 0.5 Hz) after adding media that promotes differentiation. Controls consisted of myoblasts cultured under static conditions. While miRNA expression was not affected by high stretch, a significant effect of stretch (P 0.05) was seen after 4 days with the moderate stretch regimen. All three microRNAs were upregulated by stretch, with the most significant increase for miR-1. Myoblast maturation was enhanced with a moderate stretch regimen, as assessed by a higher percentage of nuclei in straited fibers and an increase in Mef2c gene expression. Correspondingly, HDAC4 protein expression, a direct target of miR-1 and repressor of Mef2, was decreased with the moderate stretch regimen. Over-expression of miR-1 abrogated the effect of stretch on miR-1, miR-133a and miR-206 levels compared to its negative control but did not alter miR-133a or miR-206 levels. Treatment with an antisense mRNA to miR-1 similarly diminished the stretch-mediated response. Results indicate that the differential response of skeletal myoblasts to moderate and high stretch cyclic stretch regimens is due, in part, to muscle specific miRNA expression.
机译:我们检查了调节增殖(miR-133a)或分化(miR-1,-206)的机械拉伸是否影响了肌肉特异性微小RNA(miRNA)的表达。使用实时定量RT-PCR评估小鼠肌细胞细胞系C2C12中的miRNA调节,暴露于伸展方案,促进促进增殖(高弹性:17%,1 Hz)或分化(中等拉伸:10%,0.5Hz)添加促进差异化的媒体后。对照组由静态条件下培养的肌细胞组成。虽然miRNA表达不受高伸展的影响,但在4天后,延伸方案4天后会看到妊娠纹(P <0.05)的显着效果。所有三个微小RNA通过拉伸上调,MIR-1的增加升高。用中等的拉伸方案提高了肌细胞成熟,如20百分比的体系划纤维中的细胞核百分比和MEF2C基因表达的增加。相应地,HDAC4蛋白表达,MIR-1的直接靶标和MEF2的阻遏物,随着中等拉伸方案降低。 miR-1的过度表达废除了MiR-1,miR-133a和miR-206级别的效果与其阴性对照相比,但没有改变miR-133a或miR-206水平。用反义mRNA治疗miR-1类似地降低了拉伸介导的反应。结果表明,骨骼肌对中等和高拉伸循环拉伸方案的差异响应部分是肌肉特异性miRNA表达。

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