Department of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan 430062, China; Institute of Myocardial Injury and Repair, Wuhan University, Wuhan 430062, China.
Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
J Adv Res. 2024 Sep;63:117-128. doi: 10.1016/j.jare.2023.10.007. Epub 2023 Oct 6.
Cardiac hypertrophy is an important contributor of heart failure, and the mechanisms remain unclear. Leucine zipper protein 1 (LUZP1) is essential for the development and function of cardiovascular system; however, its role in cardiac hypertrophy is elusive.
This study aims to investigate the molecular basis of LUZP1 in cardiac hypertrophy and to provide a rational therapeutic approach.
Cardiac-specific Luzp1 knockout (cKO) and transgenic mice were established, and transverse aortic constriction (TAC) was used to induce pressure overload-induced cardiac hypertrophy. The possible molecular basis of LUZP1 in regulating cardiac hypertrophy was determined by transcriptome analysis. Neonatal rat cardiomyocytes were cultured to elucidate the role and mechanism of LUZP1 in vitro.
LUZP1 expression was progressively increased in hypertrophic hearts after TAC surgery. Gain- and loss-of-function methods revealed that cardiac-specific LUZP1 deficiency aggravated, while cardiac-specific LUZP1 overexpression attenuated pressure overload-elicited hypertrophic growth and cardiac dysfunction in vivo and in vitro. Mechanistically, the transcriptome data identified Stat3 pathway as a key downstream target of LUZP1 in regulating pathological cardiac hypertrophy. Cardiac-specific Stat3 deletion abolished the pro-hypertrophic role in LUZP1 cKO mice after TAC surgery. Further findings suggested that LUZP1 elevated the expression of Src homology region 2 domain-containing phosphatase 1 (SHP1) to inactivate Stat3 pathway, and SHP1 silence blocked the anti-hypertrophic effects of LUZP1 in vivo and in vitro.
We demonstrate that LUZP1 attenuates pressure overload-induced cardiac hypertrophy through inhibiting Stat3 signaling, and targeting LUZP1 may develop novel approaches to treat pathological cardiac hypertrophy.
心肌肥厚是心力衰竭的重要原因,其机制尚不清楚。亮氨酸拉链蛋白 1(LUZP1)是心血管系统发育和功能所必需的;然而,其在心肌肥厚中的作用尚不清楚。
本研究旨在探讨 LUZP1 在心肌肥厚中的分子基础,并为其提供合理的治疗方法。
建立了心脏特异性 Luzp1 敲除(cKO)和转基因小鼠,并采用主动脉缩窄(TAC)诱导压力超负荷诱导的心肌肥厚。通过转录组分析确定 LUZP1 调节心肌肥厚的可能分子基础。培养乳鼠心肌细胞以阐明 LUZP1 在体外的作用和机制。
TAC 手术后,LUZP1 的表达在肥厚的心脏中逐渐增加。增益和失能方法表明,心脏特异性 LUZP1 缺乏加重,而心脏特异性 LUZP1 过表达减轻了体内和体外压力超负荷引起的心肌肥厚和心功能障碍。从机制上讲,转录组数据将 Stat3 途径确定为 LUZP1 调节病理性心肌肥厚的关键下游靶标。心脏特异性 Stat3 缺失消除了 TAC 手术后 LUZP1 cKO 小鼠的促肥厚作用。进一步的研究结果表明,LUZP1 升高了Src 同源结构域 2 结构域磷酸酶 1(SHP1)的表达,以抑制 Stat3 途径,而 SHP1 沉默阻断了 LUZP1 在体内和体外的抗肥厚作用。
我们证明 LUZP1 通过抑制 Stat3 信号转导来减轻压力超负荷引起的心肌肥厚,靶向 LUZP1 可能为病理性心肌肥厚的治疗提供新的方法。