肌节
医学
有丝分裂
细胞生物学
生物
心肌细胞
解剖
心脏病学
内科学
作者
Feng Xiao,Ngoc Uyen Nhi Nguyen,Ping Wang,Shujuan Li,Ching‐Cheng Hsu,Suwannee Thet,Wataru Kimura,Xiang Luo,Nicholas T. Lam,Ivan Menendez-Montes,Waleed M. Elhelaly,Alisson C. Cardoso,Ana Helena Macedo Pereira,Rohit Singh,Sakthivel Sadayappan,Mohammed Kanchwala,Chao Xing,Feria A. Ladha,J. Travis Hinson,Roger J. Hajjar,Joseph A. Hill,Hesham A. Sadek
出处
期刊:Circulation
[Ovid Technologies (Wolters Kluwer)]
日期:2024-05-06
卷期号:150 (10): 791-805
标识
DOI:10.1161/circulationaha.122.059102
摘要
BACKGROUND: Recent interest in understanding cardiomyocyte cell cycle has been driven by potential therapeutic applications in cardiomyopathy. However, despite recent advances, cardiomyocyte mitosis remains a poorly understood process. For example, it is unclear how sarcomeres are disassembled during mitosis to allow the abscission of daughter cardiomyocytes. METHODS: Here, we use a proteomics screen to identify adducin, an actin capping protein previously not studied in cardiomyocytes, as a regulator of sarcomere disassembly. We generated many adeno-associated viruses and cardiomyocyte-specific genetic gain-of-function models to examine the role of adducin in neonatal and adult cardiomyocytes in vitro and in vivo. RESULTS: We identify adducin as a regulator of sarcomere disassembly during mammalian cardiomyocyte mitosis. α/γ-adducins are selectively expressed in neonatal mitotic cardiomyocytes, and their levels decline precipitously thereafter. Cardiomyocyte-specific overexpression of various splice isoforms and phospho-isoforms of α-adducin in vitro and in vivo identified Thr445/Thr480 phosphorylation of a short isoform of α-adducin as a potent inducer of neonatal cardiomyocyte sarcomere disassembly. Concomitant overexpression of this α-adducin variant along with γ-adducin resulted in stabilization of the adducin complex and persistent sarcomere disassembly in adult mice, which is mediated by interaction with α-actinin. CONCLUSIONS: These results highlight an important mechanism for coordinating cytoskeletal morphological changes during cardiomyocyte mitosis.
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