Tsui Hoyee, Zi Min, Wang Shunyao, Chowdhury Sanjoy K, Prehar Sukhpal, Liang Qiangrong, Cartwright Elizabeth J, Lei Ming, Liu Wei, Wang Xin
From the Faculty of Life Sciences (H.T, S.W., S.K.C., W.L., X.W.) and Faculty of Medical and Human Sciences (M.Z., S.P., E.J.C.), University of Manchester, Manchester, United Kingdom; Department of Biomedical Sciences, New York Institute of Technology, NY (Q.L.); and Department of Pharmacology, University of Oxford, Oxford, United Kingdom (M.L.).
Hypertension. 2015 Dec;66(6):1176-83. doi: 10.1161/HYPERTENSIONAHA.115.06068. Epub 2015 Oct 19.
Pathological cardiac hypertrophy is regarded as a critical intermediate step toward the development of heart failure. Many signal transduction cascades are demonstrated to dictate the induction and progression of pathological hypertrophy; however, our understanding in regulatory mechanisms responsible for the suppression of hypertrophy remains limited. In this study, we showed that exacerbated hypertrophy induced by pressure overload in cardiac-deleted Pak1 mice was attributable to a failure to upregulate the antihypertrophic E3 ligase, Fbxo32, responsible for targeting proteins for the ubiquitin-degradation pathway. Under pressure overload, cardiac overexpression of constitutively active Pak1 mice manifested strong resilience against pathological hypertrophic remodeling. Mechanistic studies demonstrated that subsequent to Pak1 activation, the binding of Smad3 on a critical singular AGAC(-286)-binding site on the FBXO32 promoter was crucial for its transcriptional regulation. Pharmacological upregulation of Fbxo32 by Berberine ameliorated hypertrophic remodeling and improved cardiac performance in cardiac-deficient Pak1 mice under pressure overload. Our findings discover Smad3 and Fbxo32 as novel downstream components of the Pak1-dependent signaling pathway for the suppression of hypertrophy. This discovery opens a new venue for opportunities to identify novel targets for the management of cardiac hypertrophy.
病理性心脏肥大被认为是心力衰竭发展过程中的一个关键中间步骤。许多信号转导级联反应已被证明可决定病理性肥大的诱导和进展;然而,我们对负责抑制肥大的调节机制的理解仍然有限。在本研究中,我们发现心脏特异性敲除Pak1基因的小鼠在压力超负荷诱导下出现的肥大加剧,是由于未能上调负责将蛋白质靶向泛素降解途径的抗肥大E3连接酶Fbxo32。在压力超负荷情况下,组成型活性Pak1基因过表达的小鼠心脏表现出对病理性肥大重塑的强大抵抗力。机制研究表明,Pak1激活后,Smad3与FBXO32启动子上一个关键的单一AGAC(-286)结合位点的结合对其转录调控至关重要。在压力超负荷情况下,黄连素对心脏特异性缺失Pak1基因的小鼠进行Fbxo32的药理学上调,可改善肥大重塑并提高心脏功能。我们的研究结果发现Smad3和Fbxo32是Pak1依赖性信号通路中抑制肥大的新下游成分。这一发现为识别心脏肥大治疗新靶点提供了新途径。