Ding Jie, Yang Anqi, Zhou Liping, Zhang Fulei, Zhou Huixing, Zhang Yuemei, Wang Yan, Liu Yi, Liang Dandan, Liu Yuanyuan, Wu Yahan
Department of Cardiology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China.
Jinzhou Medical University, Jinzhou, 121000, China.
J Cardiovasc Transl Res. 2025 Mar 17. doi: 10.1007/s12265-025-10604-3.
Cardiomyocyte hypertrophy is a key remodeling response to cardiac stress and an independent risk factor for heart failure. However, the molecular mechanism of cardiomyocyte hypertrophy is not yet fully understood. We here found Polo-like kinase 1 (PLK1) was crucial in regulating endothelin-1 (ET-1)-induced cardiomyocyte hypertrophy. Notably, PLK1 expression was significantly elevated in ET-1-induced hypertrophic cardiomyocytes and pressure overload-induced hypertrophic cardiac tissue. Knocking down Plk1 reduced the cell size of hypertrophic cardiomyocytes and suppressed the expression of hypertrophic markers, including ANP, BNP and β-MHC. The PLK1 inhibitor BI2536 had similar effects on hypertrophic cardiomyocytes. Mechanistically, the ERK1/2 pathway was identified as the key downstream pathway mediating the effects of PLK1 on ET-1-induced cardiomyocyte hypertrophy. Finally, the deficiency of PLK1 attenuated the hypertrophy of hiPSC-CMs. In summary, our study revealed that PLK1 regulates ET-1-induced cardiomyocyte hypertrophy through the ERK1/2 pathway, providing insights into the pathogenesis and potential therapies for pathological cardiac hypertrophy.
心肌细胞肥大是心脏应激的关键重塑反应,也是心力衰竭的独立危险因素。然而,心肌细胞肥大的分子机制尚未完全阐明。我们在此发现,Polo样激酶1(PLK1)在调节内皮素-1(ET-1)诱导的心肌细胞肥大中起关键作用。值得注意的是,在ET-1诱导的肥大心肌细胞和压力超负荷诱导的肥大心脏组织中,PLK1表达显著升高。敲低Plk1可减小肥大心肌细胞的大小,并抑制包括ANP、BNP和β-MHC在内的肥大标志物的表达。PLK1抑制剂BI2536对肥大心肌细胞有类似作用。从机制上讲,ERK1/2通路被确定为介导PLK1对ET-1诱导的心肌细胞肥大作用的关键下游通路。最后,PLK1的缺乏减轻了人诱导多能干细胞来源的心肌细胞(hiPSC-CMs)的肥大。总之,我们的研究表明,PLK1通过ERK1/2通路调节ET-1诱导的心肌细胞肥大,为病理性心肌肥大的发病机制和潜在治疗提供了见解。