首页> 外文期刊>Journal of cellular and molecular medicine. >Nucleolin promotes Ang II‐induced phenotypic transformation of vascular smooth muscle cells by regulating EGF and PDGF‐BB
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Nucleolin promotes Ang II‐induced phenotypic transformation of vascular smooth muscle cells by regulating EGF and PDGF‐BB

机译:通过调节EGF和PDGF-BB,核仁促进血管平滑肌细胞的Ang II诱导的血管平滑肌细胞的表型转化

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RNA‐binding properties of nucleolin play a fundamental role in regulating cell growth and proliferation. We have previously shown that nucleolin plays an important regulatory role in the phenotypic transformation of vascular smooth muscle cells (VSMCs) induced by angiotensin II (Ang II). In the present study, we aimed to investigate the molecular mechanism of nucleolin‐mediated phenotypic transformation of VSMCs induced by Ang II. Epidermal growth factor (EGF) and platelet‐derived growth factor (PDGF) inhibitors were used to observe the effect of Ang II on phenotypic transformation of VSMCs. The regulatory role of nucleolin in the phenotypic transformation of VSMCs was identified by nucleolin gene mutation, gene overexpression and RNA interference technology. Moreover, we elucidated the molecular mechanism underlying the regulatory effect of nucleolin on phenotypic transformation of VSMCs. EGF and PDGF‐BB played an important role in the phenotypic transformation of VSMCs induced by Ang II. Nucleolin exerted a positive regulatory effect on the expression and secretion of EGF and PDGF‐BB. In addition, nucleolin could bind to the 5′ untranslated region (UTR) of EGF and PDGF‐BB mRNA, and such binding up‐regulated the stability and expression of EGF and PDGF‐BB mRNA, promoting Ang II‐induced phenotypic transformation of VSMCs.
机译:核仁的RNA结合特性在调节细胞生长和增殖中起着基本作用。我们之前已经表明,核仁患者在血管紧张素II(ANG II)诱导的血管平滑肌细胞(VSMC)的表型转化中起重要的调节作用。在本研究中,我们旨在探讨核仁介导的Ang II诱导的VSMC表型转化的分子机制。表皮生长因子(EGF)和血小板衍生的生长因子(PDGF)抑制剂用于观察Ang II对VSMC的表型转化的影响。通过核仁基因突变,基因过表达和RNA干扰技术鉴定了核素在VSMC表型转化中的调节作用。此外,我们阐明了核仁核心对VSMC表型转化的调节作用的分子机制。 EGF和PDGF-BB在Ang II诱导的VSMC的表型转化中发挥着重要作用。核仁施加了对EGF和PDGF-BB的表达和分泌的阳性调节作用。此外,核仁可以结合EGF和PDGF-BB mRNA的5'未转换区域(UTR),并且如此结合上调EGF和PDGF-BB mRNA的稳定性和表达,促进VSMC的Ang II诱导的表型转化。

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