Adducin 在心肌细胞有丝分裂过程中调控肌节分解

IF 35.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation Pub Date : 2024-09-03 Epub Date: 2024-05-06 DOI:10.1161/CIRCULATIONAHA.122.059102
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 Campos 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
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引用次数: 0

摘要

背景:最近,人们对心肌细胞周期的了解兴趣主要来自心肌病的潜在治疗应用。然而,尽管最近取得了一些进展,但人们对心肌细胞有丝分裂过程的了解仍然很少。例如,目前还不清楚有丝分裂过程中肌节是如何解体以允许子心肌细胞脱落的。方法:在这里,我们利用蛋白质组学筛选鉴定了adducin--一种以前未在心肌细胞中研究过的肌动蛋白盖蛋白--作为肌节解体的调节因子。我们生成了许多腺相关病毒和心肌细胞特异性基因功能增益模型,以研究adducin在新生儿和成年心肌细胞体外和体内的作用:结果:我们发现adducin是哺乳动物心肌细胞有丝分裂过程中肌节分解的调节因子。心肌细胞特异性过表达α-adducin的各种剪接异构体和磷酸化异构体后发现,α-adducin短异构体的Thr445/Thr480磷酸化是新生儿心肌细胞肌节解体的有效诱导因素。同时过表达这种α-adducin变体和γ-adducin会导致adducin复合物的稳定和成年小鼠持续的肌节解体,而这是通过与α-actinin的相互作用介导的:这些结果突显了心肌细胞有丝分裂过程中协调细胞骨架形态变化的重要机制。
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Adducin Regulates Sarcomere Disassembly During Cardiomyocyte Mitosis.

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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来源期刊
Circulation
Circulation 医学-外周血管病
CiteScore
45.70
自引率
2.10%
发文量
1473
审稿时长
2 months
期刊介绍: Circulation is a platform that publishes a diverse range of content related to cardiovascular health and disease. This includes original research manuscripts, review articles, and other contributions spanning observational studies, clinical trials, epidemiology, health services, outcomes studies, and advancements in basic and translational research. The journal serves as a vital resource for professionals and researchers in the field of cardiovascular health, providing a comprehensive platform for disseminating knowledge and fostering advancements in the understanding and management of cardiovascular issues.
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