Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
J Cell Physiol. 2019 Aug;234(8):13680-13692. doi: 10.1002/jcp.28047. Epub 2019 Jan 3.
Cardiac hypertrophy and its resultant heart failure are among the most common causes of mortality, worldwide. Long noncoding RNAs (lncRNAs) are involved in diverse biological processes, and their vital role in the regulation of cardiac hypertrophy is increasingly being discovered. Nevertheless, the biological roles of lncRNA X-inactive specific transcript (XIST) in cardiac hypertrophy are scarcely reported, and the current study was designed to determine whether cardiac hypertrophy can be regulated by XIST and to elucidate the related mechanism. The animals were randomized to receive either an adeno-associated virus expressing XIST or control plasmid via a single bolus-tail vein injection. Two weeks later, hypertrophy was established by transverse aortic constriction (TAC) surgery. In vitro, H9c2 cells were used to explore the potential molecular mechanism of XIST in the regulation of phenylephrine (PE)-induced cardiomyocyte hypertrophy. A luciferase reporter assay and RNA immunoprecipitation were performed to explore the relationships among XIST, microRNA (miR)-101, and toll-like receptor 2 (TLR2). In this study, we demonstrated that the expression of XIST was significantly upregulated in hypertrophic mouse hearts and PE-treated cardiomyocytes. Then, we observed that knockdown of XIST attenuated PE-induced cardiomyocyte hypertrophy. Conversely, overexpression of XIST aggravated TAC-induced cardiac hypertrophy. Finally, we demonstrated that miR-101 was a direct target of XIST, whereas TLR2 was a target of miR-101. Rescue assays further confirmed that XIST promoted the progression of cardiac hypertrophy through competitively binding with miR-101 to enhance the expression of TLR2. Collectively, these in vivo and in vitro findings identify XIST as a necessary regulator of cardiac hypertrophy due to its regulation of the miR-101/TLR2 axis, suggesting that XIST might act as a therapeutic target for the treatment of cardiac hypertrophy and heart failure.
心肌肥厚及其导致的心力衰竭是全球范围内最常见的死亡原因之一。长链非编码 RNA(lncRNA)参与多种生物学过程,其在心肌肥厚调控中的重要作用正逐渐被发现。然而,lncRNA X 染色体失活特异性转录物(XIST)在心肌肥厚中的生物学作用鲜有报道,本研究旨在确定心肌肥厚是否可以受 XIST 调控,并阐明相关机制。动物随机接受腺相关病毒表达 XIST 或对照质粒通过单次尾静脉注射。2 周后,通过横主动脉缩窄(TAC)手术建立肥厚模型。在体外,使用 H9c2 细胞探索 XIST 调节苯肾上腺素(PE)诱导的心肌细胞肥厚的潜在分子机制。进行荧光素酶报告基因检测和 RNA 免疫沉淀实验以探索 XIST、微小 RNA(miR)-101 和 Toll 样受体 2(TLR2)之间的关系。在本研究中,我们证明了 XIST 在肥厚小鼠心脏和 PE 处理的心肌细胞中的表达显著上调。然后,我们观察到敲低 XIST 可减弱 PE 诱导的心肌细胞肥大。相反,过表达 XIST 加重 TAC 诱导的心脏肥大。最后,我们证明 miR-101 是 XIST 的直接靶标,而 TLR2 是 miR-101 的靶标。挽救实验进一步证实,XIST 通过与 miR-101 竞争性结合来增强 TLR2 的表达,从而促进心脏肥大的进展。总之,这些体内和体外研究结果表明,由于 XIST 调节 miR-101/TLR2 轴,因此 XIST 是心肌肥厚的必要调节因子,表明 XIST 可能作为治疗心肌肥厚和心力衰竭的治疗靶点。