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WNT signaling in adult cardiac hypertrophy and remodeling: lessons learned from cardiac development.

机译:成人心脏肥大和重塑中的WNT信号传导:从心脏发育中学到的经验教训。

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摘要

On pathological stress, the heart reactivates several signaling pathways that traditionally were thought to be operational only in the developing heart. One of these pathways is the WNT signaling pathway. WNT controls heart development but is also modulated during adult heart remodeling. This review summarizes the currently available data regarding WNT signaling during left ventricular (LV) remodeling. Upstream, soluble frizzled-related proteins (sFRPs) block WNT-dependent activation of the canonical WNT pathway. By inhibition of WNT activation, these factors also reduce beta-catenin-dependent transcription by altering the ratio of cytoplasmicuclear beta-catenin. In experimental settings, sFRPs injected into the heart attenuated LV remodeling. sFRPs are secreted from autologous bone marrow-derived mononuclear cells. Disheveled is a signaling intermediate of both the canonical and noncanonical WNT pathway. Similarly to the effect of sFRP, depletion of a disheveled isoform attenuated LV remodeling. In contrast, disheveled activation led to progressive dilated cardiomyopathy. Inhibition of nuclear beta-catenin signaling downstream of the canonical WNT pathway significantly reduced postinfarct mortality and functional decline of LV function following chronic left anterior descending coronary artery ligation. WNT signaling also affects mobilization and homing of bone marrow-derived vasculogenic progenitor cells. Finally, heart-specific WNT/beta-catenin interaction partners have been identified that will possibly allow targeting this pathway in a tissue-specific manner. In summary, the WNT pathway plays a pivotal role in adult cardiac remodeling and may be suitable for therapeutic interventions. Currently, several molecular and cellular mechanisms whereby WNT inhibition attenuates LV remodeling are proposed. Reactivation of the developmental program to restore functional LV myocardium from resident precursor cells may significantly contribute to this process.
机译:在病理性压力下,心脏会重新激活传统上仅在发育中的心脏才起作用的几种信号通路。这些途径之一是WNT信号传导途径。 WNT控制心脏发育,但在成人心脏重塑期间也会受到调节。这篇综述总结了有关左心室(LV)重塑期间WNT信号传导的当前可用数据。上游,可溶性卷曲相关蛋白(sFRP)阻止经典WNT途径的WNT依赖性激活。通过抑制WNT激活,这些因子还通过改变细胞质/核β-连环蛋白的比例来减少β-连环蛋白依赖性转录。在实验设置中,注入心脏的sFRP减弱了LV重塑。 sFRP从自体骨髓来源的单核细胞分泌。杂散的是经典和非经典WNT途径的信号传导中间产物。与sFRP的作用类似,蓬乱的同工型的耗竭会减弱LV重塑。相反,不整齐的激活导致进行性扩张型心肌病。慢性左冠状动脉前降支结扎后,经典WNT途径下游核β-catenin信号的抑制显着降低了梗死后死亡率和LV功能的功能下降。 WNT信号还影响骨髓来源的血管生成祖细胞的动员和归巢。最后,已经确定了心脏特异性WNT /β-catenin相互作用伴侣,这可能允许以组织特异性方式靶向该途径。总之,WNT途径在成人心脏重塑中起着关键作用,可能适合治疗性干预。当前,提出了几种分子和细胞机制,其中WNT抑制减弱了LV重塑。重新启动发育程序以从驻留的前体细胞恢复功能性LV心肌可能会大大促进这一过程。

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