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Screening and functional prediction of differentially expressed circRNAs in proliferative human aortic smooth muscle cells

机译:增殖性人主动脉平滑肌细胞中差异表达circRNA的筛选和功能预测

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摘要

Vascular smooth muscle cell (VSMC) proliferation is the pathological base of vascular remodelling diseases. Circular RNAs (circRNAs) are important regulators involved in various biological processes. However, the function of circRNAs in VSMC proliferation regulation remains largely unknown. This study was conducted to identify the key differentially expressed circRNAs (DEcircRNAs) and predict their functions in human aortic smooth muscle cell (HASMC) proliferation. To achieve this, DEcircRNAs between proliferative and quiescent HASMCs were detected using a microarray, followed by quantitative real‐time RT‐PCR validation. A DEcircRNA‐miRNA‐DEmRNA network was constructed, and functional annotation was performed using Gene Ontology (GO) and KEGG pathway analysis. The function of hsa_circ_0002579 in HASMC proliferation was analysed by Western blot. The functional annotation of the DEcircRNA‐miRNA‐DEmRNA network indicated that the four DEcircRNAs might play roles in the TGF‐β receptor signalling pathway, Ras signalling pathway, AMPK signalling pathway and Wnt signalling pathway. Twenty‐seven DEcircRNAs with coding potential were screened. Hsa_circ_0002579 might be a pro‐proliferation factor of HASMC. Overall, our study identified the key DEcircRNAs between proliferative and quiescent HASMCs, which might provide new important clues for exploring the functions of circRNAs in vascular remodelling diseases.
机译:血管平滑肌细胞(VSMC)的增殖是血管重塑疾病的病理基础。环状RNA(circRNA)是参与各种生物学过程的重要调节剂。但是,circRNA在VSMC增殖调控中的功能仍然未知。进行这项研究以鉴定关键差异表达的circRNA(DEcircRNA),并预测其在人主动脉平滑肌细胞(HASMC)增殖中的功能。为此,使用微阵列检测了增殖和静止HASMC之间的DEcircRNA,然后进行了实时定量RT-PCR验证。构建了一个DEcircRNA-miRNA-DEmRNA网络,并使用基因本体论(GO)和KEGG途径分析进行功能注释。通过蛋白质印迹分析了hsa_circ_0002579在HASMC增殖中的功能。 DEcircRNA-miRNA-DEmRNA网络的功能注释表明这四个DEcircRNA可能在TGF-β受体信号通路,Ras信号通路,AMPK信号通路和Wnt信号通路中起作用。筛选了27个具有编码潜能的DEcircRNA。 Hsa_circ_0002579可能是HASMC的扩散因子。总的来说,我们的研究确定了增生和静止HASMC之间的关键DEcircRNA,这可能为探索circRNA在血管重塑疾病中的功能提供新的重要线索。

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