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首页> 外文期刊>International Journal of Molecular Sciences >Gga-miR-3525 Targets PDLIM3 through the MAPK Signaling Pathway to Regulate the Proliferation and Differentiation of Skeletal Muscle Satellite Cells
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Gga-miR-3525 Targets PDLIM3 through the MAPK Signaling Pathway to Regulate the Proliferation and Differentiation of Skeletal Muscle Satellite Cells

机译:GGA-MIR-3525通过MAPK信号通路靶向PDLIM3,以调节骨骼肌卫星细胞的增殖和分化

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MicroRNAs (miRNAs) are evolutionarily conserved, small noncoding RNAs that post-transcriptionally regulate expression of their target genes. Emerging evidence demonstrates that miRNAs are important regulators in the development of skeletal muscle satellite cells (SMSCs). Our previous research showed that gga-miR-3525 is differentially expressed in breast muscle of broilers (high growth rate) and layers (low growth rate). In this study, we report a new role for gga-miR-3525 as a myogenic miRNA that regulates skeletal muscle development in chickens. Exogenous increases in the expression of gga-miR-3525 significantly inhibited proliferation and differentiation of SMSCs, whereas the opposite effects were observed in gga-miR-3525 knockdown SMSCs. We confirmed that PDLIM3 (PDZ and LIM domain 3) is a target gene of gga-miR-3525 that can promote proliferation and differentiation of SMSCs. We found that PDLIM3 overexpression elevated the abundance of phosphorylated (p-)p38 protein but that the gga-miR-3525 mimic and p38-MAPK inhibitor (SB203580) weakened the activation of p-p38. Furthermore, treatment with SB203580 reduced the promoting effect of PDLIM3 on SMSC proliferation and differentiation. Overall, our results indicate that gga-miR-3525 regulates the proliferation and differentiation of SMSCs by targeting PDLIM3 via the p38/MAPK signaling pathway in chickens.
机译:MicroRNAS(miRNA)进化地保守,小非编码RNA,后转录调节其靶基因的表达。新兴的证据表明,MiRNA是在骨骼肌卫星细胞(SMSCs)的发展中的重要调节因素。我们以前的研究表明,GGA-MIR-3525在肉鸡(高生长率)和层(低生长速率)中差异表达。在这项研究中,我们向GGA-MIR-3525报告了新的作用作为调节鸡骨骼肌发育的肌菌MiRNA。外源性增加GGA-miR-3525的表达显着抑制SMSC的增殖和分化,而在GGA-miR-3525敲低SMSCs中观察到相反的效果。我们确认PDLIM3(PDZ和LIM结构域3)是GGA-MIR-3525的靶基因,其可促进SMSCs的增殖和分化。我们发现PDLIM3过表达升高了磷酸化(P-)P38蛋白的丰度,但GGA-MIR-3525模拟和P38-MAPK抑制剂(SB203580)削弱了P-P38的活化。此外,用SB203580治疗降低了PDLIM3对SMSC增殖和分化的促进作用。总体而言,我们的结果表明,GGA-miR-3525通过鸡中的P38 / MAPK信号通路来调节SMSCs的增殖和分化。

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