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首页> 外文期刊>Journal of Molecular and Cellular Cardiology >LncRNA-Mhrt regulates cardiac hypertrophy by modulating the miR-145a-5p/KLF4/myocardin axis
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LncRNA-Mhrt regulates cardiac hypertrophy by modulating the miR-145a-5p/KLF4/myocardin axis

机译:通过调节miR-145a-5p / klf4 / myocardin轴来调节心脏肥大来调节心肌肥厚

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摘要

Cardiac hypertrophy is an early milestone of many heart diseases. LncRNAs often play a leading role in this process. However, its mechanism of action in cardiac hypertrophy has not been fully explained. In a previous study, we showed a new mode by which lncRNA-Mhrt inhibited cardiac hypertrophy by inhibiting myocardin. However, the underlying molecular mechanism remains unclear. This study aims to explore potential action modes of Mhrt in regulating the expression of myocardin in the process of cardiac hypertrophy. Here, we find that Mhrt reduces myocardin expression through KLF4 in vivo and in vitro. Meanwhile, Mhrt promotes the expression of KLF4 through direct binding to miR-145a-5p or inhibiting phosphorylation of KLF4 by forming a complex with KLF4 to prevent the binding of ERK and KLF4, thereby inhibiting myocardin expression and the development of myocardial hypertrophy. Taken together, our findings reveal a new pathway, Mhrt-KLF4-myocardin, that regulates cardiac hypertrophy and revealed additional possible action modes of Mhrt in the occurrence and development of cardiac hypertrophy. The new regulatory pathway serves as a potential therapeutic avenue for cardiac hypertrophy.
机译:心脏肥大是许多心脏病的早期里程碑。 LNCRNA经常在这个过程中发挥主导作用。然而,它在心脏肥大中的作用机制尚未得到充分解释。在先前的研究中,我们展示了一种新的模式,通过抑制心肌蛋白,LNCRNA-MHRT抑制心脏肥厚。然而,潜在的分子机制仍然尚不清楚。本研究旨在探讨MHRT在心肌肥厚过程中调节心肌蛋白表达的潜在动作模式。在这里,我们发现MHRT通过体内和体外通过KLF4减少了Myocardin表达。同时,MHRT通过直接结合MIR-145A-5P促进KLF4的表达或通过形成与KLF4的复合物来抑制KLF4的磷酸化以防止ERK和KLF4的结合,从而抑制心肌蛋白的表达和心肌肥大的发展。我们的研究结果一起揭示了一种新的途径MHRT-KLF4-Myocardin,调节心脏肥大,并在心脏肥大的发生和发展中揭示了MHRT的额外动作模式。新的监管途径用作心肌肥厚的潜在治疗途径。

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