Targeting myomiRs by tocotrienol-rich fraction to promote myoblast differentiation.

Genes & Nutrition Pub Date : 2018-11-29 eCollection Date: 2018-01-01 DOI:10.1186/s12263-018-0618-2
Azraul Mumtazah Razak, Shy Cian Khor, Faizul Jaafar, Norwahidah Abdul Karim, Suzana Makpol
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引用次数: 5

Abstract

Background: Several muscle-specific microRNAs (myomiRs) are differentially expressed during cellular senescence. However, the role of dietary compounds on myomiRs remains elusive. This study aimed to elucidate the modulatory role of tocotrienol-rich fraction (TRF) on myomiRs and myogenic genes during differentiation of human myoblasts. Young and senescent human skeletal muscle myoblasts (HSMM) were treated with 50 μg/mL TRF for 24 h before and after inducing differentiation.

Results: The fusion index and myotube surface area were higher (p < 0.05) on days 3 and 5 than that on day 1 of differentiation. Ageing reduced the differentiation rate, as observed by a decrease in both fusion index and myotube surface area in senescent cells (p < 0.05). Treatment with TRF significantly increased differentiation at days 1, 3 and 5 of young and senescent myoblasts. In senescent myoblasts, TRF increased the expression of miR-206 and miR-486 and decreased PTEN and PAX7 expression. However, the expression of IGF1R was upregulated during early differentiation and decreased at late differentiation when treated with TRF. In young myoblasts, TRF promoted differentiation by modulating the expression of miR-206, which resulted in the reduction of PAX7 expression and upregulation of IGF1R.

Conclusion: TRF can potentially promote myoblast differentiation by modulating the expression of myomiRs, which regulate the expression of myogenic genes.

Abstract Image

Abstract Image

Abstract Image

富生育三烯醇部位靶向myomir促进成肌细胞分化。
背景:几种肌肉特异性microRNAs (myomiRs)在细胞衰老过程中差异表达。然而,膳食化合物在myomir中的作用仍然难以捉摸。本研究旨在阐明富生育三烯醇组分(TRF)在人成肌细胞分化过程中对myomir和肌源性基因的调节作用。分别用50 μg/mL TRF处理年轻和衰老人骨骼肌成肌细胞诱导分化前后24 h。结果:miR-206和miR-486的融合指数和肌管表面积升高(p < 0.05), PTEN和PAX7的表达降低。然而,在TRF处理下,IGF1R的表达在早期分化时上调,在晚期分化时降低。在年轻的成肌细胞中,TRF通过调节miR-206的表达促进分化,从而导致PAX7的表达减少和IGF1R的上调。结论:TRF可能通过调节myomir的表达而促进成肌细胞分化,而myomir可调节成肌基因的表达。
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