Department of Cardiovascular Medicine, Baoji People's Hospital, Baoji City, Shaanxi Province, China.
Department of Cardiology, Baoji Chinese Medicine Hospital, Baoji City, Shaanxi Province, China.
Bioengineered. 2021 Dec;12(2):9655-9667. doi: 10.1080/21655979.2021.1977552.
Myocardial hypertrophy is a pathological thickening of the myocardium, leading to various ailments, such as myocardial infarction and heart failure. RBM38 is critical in modulating mRNA translation for multiple protective activities such as p53 tumor repressor and p21 kinase cell cycle inhibitors. Liver X receptors (LXR-α) agonists reduce cellular hypertrophy initiated by various hypertrophic stimuli as lipopolysaccharides and Ang II. This research investigates the possible cooperation between RBM38 and LXR-α and mechanisms in modulating myocardial hypertrophy. H9C2 cells were treated with PE, TNF-α, and AngII to induce myocardial hypertrophy. RBM38 and LXR- α were overexpressed or silenced in H9C2 cells, and hypertrophy markers (ANF and Myh7) were determined with Western blot and RT-qPCR. Binding assays were done through RNA immunoprecipitation. H&E and Rhodamine-labeled phalloidin staining assays were used to assess the relative cell surface change. The results demonstrated RBM38 downregulation in in vitro models of myocardial hypertrophy. Modulation of RBM38 expression also exerted inverse effects on myocardial hypertrophy markers. Further observations also showed that LXR-α expression regulates the myocardial hypertrophy markers in H9C2 cells and RBM38 binds with LXR-α mRNA, consequently inhibiting LXR-α expression. Finally, overexpression of RBM38 rescues Angiotensin II-induced myocardial hypertrophy by regulating LXR-α dependent lipogenesis pathway. In conclusion, RBM38 Overexpression rescues Angiotensin II-induced myocardial hypertrophy by regulating LXR-α dependent lipogenesis pathway.
心肌肥厚是心肌的病理性增厚,导致各种疾病,如心肌梗死和心力衰竭。RBM38 对于调节多种保护活性的 mRNA 翻译至关重要,例如 p53 肿瘤抑制剂和 p21 激酶细胞周期抑制剂。肝 X 受体 (LXR-α) 激动剂可减少脂多糖和 Ang II 等各种肥大刺激引发的细胞肥大。本研究探讨了 RBM38 和 LXR-α 之间的可能合作以及调节心肌肥厚的机制。用 PE、TNF-α 和 AngII 处理 H9C2 细胞以诱导心肌肥大。在 H9C2 细胞中过表达或沉默 RBM38 和 LXR-α,并通过 Western blot 和 RT-qPCR 测定肥大标志物(ANF 和 Myh7)。通过 RNA 免疫沉淀进行结合测定。通过 H&E 和罗丹明标记鬼笔环肽染色测定评估相对细胞表面变化。结果表明,体外心肌肥厚模型中 RBM38 的下调。RBM38 表达的调节也对心肌肥厚标志物产生相反的影响。进一步的观察还表明,LXR-α 表达调节 H9C2 细胞中的心肌肥厚标志物,并且 RBM38 与 LXR-α mRNA 结合,从而抑制 LXR-α 的表达。最后,通过调节 LXR-α 依赖性脂肪生成途径,RBM38 的过表达可挽救血管紧张素 II 诱导的心肌肥厚。总之,RBM38 的过表达通过调节 LXR-α 依赖性脂肪生成途径挽救血管紧张素 II 诱导的心肌肥厚。