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Expression profiles and potential roles of transfer RNA-derived small RNAs in atherosclerosis

机译:在动脉粥样硬化中转移RNA衍生的小RNA的表达谱和潜在作用

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Knowledge regarding the relationship between the molecular mechanisms underlying atherosclerosis (AS) and transfer RNA-derived small RNAs (tsRNAs) is limited. This study illustrated the expression profile of tsRNAs, thus exploring its roles in AS pathogenesis. Small RNA sequencing was performed with four atherosclerotic arterial and four healthy subject samples. Using bioinformatics, the protein-protein interaction network and cellular experiments were constructed to predict the enriched signalling pathways and regulatory roles of tsRNAs in AS. Of the total 315 tsRNAs identified to be dysregulated in the AS group, 131 and 184 were up-regulated and down-regulated, respectively. Interestingly, the pathway of the differentiated expression of tsRNAs in cell adhesion molecules (CAMs) was implicated to be closely associated with AS. Particularly, tRF-Gly-GCC might participate in AS pathogenesis via regulating cell adhesion, proliferation, migration and phenotypic transformation in HUVECs and VSMCs. In conclusion, tsRNAs might help understand the molecular mechanisms of AS better. tRF-Gly-GCC may be a promising target for suppressing abnormal vessels functions, suggesting a novel strategy for preventing the progression of atherosclerosis.
机译:关于动脉粥样硬化(AS)和转移RNA衍生的小RNA(TSRNA)之间的分子机制关系的知识受到限制。本研究说明了TSRNA的表达谱,从而探讨其作用作为发病机制。用四个动脉粥样硬化动脉和四个健康对象样品进行小RNA测序。使用生物信息学,构建蛋白质 - 蛋白质相互作用网络和细胞实验以预测TSRNA的富集的信号通路和调节作用。在AS组,131和184中鉴定的315个TSRNA分别被上调和下调。有趣的是,细胞粘附分子(凸轮)中TsRNA的分化表达的途径涉及与如此密切相关。特别地,TRF-GLY-GCC可能通过调节HUVECS和VSMCs中的细胞粘附,增殖,迁移和表型转化作为发病机制。总之,Tsrnas可能有助于了解更好的分子机制。 TRF-GLY-GCC可能是抑制异常血管功能的有希望的靶标,这表明预防动脉粥样硬化进展的新策略。

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