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首页> 外文期刊>Molecular medicine reports >Downregulation of miR-146a promotes proliferation and migration of AOB-treated embryoid body via PDGFRA induction
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Downregulation of miR-146a promotes proliferation and migration of AOB-treated embryoid body via PDGFRA induction

机译:miR-146a的下调促进通过PDGFRA诱导促进AOB处理的胚状体的增殖和迁移

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摘要

Antioxidant of bamboo leaves (AOB) has been proven to have antioxidant activity and an inhibitory effect on free radicals that induce deterioration of macromolecules. The multi-target regulation of microRNAs (miRs) in the complicated process of vasculogenesis and angiogenesis lead to the use of miRNA therapy in vascular development. In the present study, the role of miRNAs on early embryo vascular development upon AOB stimulation was investigated. For this purpose, mouse embryonic stem cells were spontaneously differentiated as embryoid bodies (EBs) and were examined by phase contrast microscopy. miR-146a mimic and scramble control were transfected into EBs and potential targets of miR-146a were predicted. Cell proliferation and migration were detected by cell viability and wound-healing and migration assays, respectively. Angiogenesis was determined by the Spheroid sprouting assay. It was demonstrated that EBs transfected with miR-146a mimic had an increased growth rate compared with the control cells. miR-146a-transfected cells were very susceptible to AOB treatment. Furthermore, among the predicted miR-146a targets, platelet-derived growth factor receptor alpha (PDGFRA) was identified as a bona fide target of miR-146a. In conclusion, PDGFRA was demonstrated to participate in the modulation of cell migration and proliferation of mouse EBs. The present study expanded the current understanding of AOB biology and elucidated the mechanisms underlying early embryo vascular development upon AOB stimulation.
机译:竹叶(AOB)的抗氧化剂已被证明具有抗氧化活性和对诱导大分子劣化的自由基的抑制作用。微大血管生成和血管生成过程中微大稻草(MIR)的多目标调节导致MiRNA治疗在血管发育中的使用。在本研究中,研究了MiRNA对艾博刺激刺激早期胚胎血管发育的作用。为此目的,小鼠胚胎干细胞被自发地分化为胚状体(EBS),并通过相位对比显微镜检查。将MiR-146A模拟和争夺对照转染到EBS中,预测MIR-146A的潜在目标。通过细胞活力和伤口愈合和迁移测定分别检测细胞增殖和迁移。血管生成由球状发芽测定确定。据证明,与对照细胞相比,用miR-146a模仿转染的EBs具有增加的生长速率。 miR-146a-转染的细胞非常易于Aob治疗。此外,在预测的miR-146a靶标中,血小板衍生的生长因子受体α(pdgfra)被鉴定为miR-146a的真绒靶。总之,PDGFRA被证明参与小鼠EBS细胞迁移和增殖的调节。本研究扩大了对AOB生物学的目前的认识,并阐明了AOB刺激后早期胚胎血管发育的机制。

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