肌丝
收缩性
磷酸化
心力衰竭
心脏病学
内科学
细胞生物学
医学
信号转导
生物
心肌细胞
作者
Ying Wang,Meimi Zhao,Xianhui Liu,Bing Xu,Gopireddy R. Reddy,Aleksandra Jovanović,Qingtong Wang,Chaoqun Zhu,Heli Xu,Elizabeth F. Bayne,Wenjing Xiang,Douglas G. Tilley,Ying Ge,Christopher G. Tate,Robert Feil,Joanna C. Chiu,Donald M. Bers,Yang Xiang
标识
DOI:10.1016/j.jacbts.2024.03.007
摘要
Phosphorylation of myofilament proteins critically regulates beat-to-beat cardiac contraction and is typically altered in heart failure (HF). β-Adrenergic activation induces phosphorylation in numerous substrates at the myofilament. Nevertheless, how cardiac β-adrenoceptors (βARs) signal to the myofilament in healthy and diseased hearts remains poorly understood. The aim of this study was to uncover the spatiotemporal regulation of local βAR signaling at the myofilament and thus identify a potential therapeutic target for HF. Phosphoproteomic analysis of substrate phosphorylation induced by different βAR ligands in mouse hearts was performed. Genetically encoded biosensors were used to characterize cyclic adenosine and guanosine monophosphate signaling and the impacts on excitation-contraction coupling induced by β
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