TY - JOUR
T1 - Adducin Regulates Sarcomere Disassembly During Cardiomyocyte Mitosis
AU - Xiao, Feng
AU - Nguyen, Ngoc Uyen Nhi
AU - Wang, Ping
AU - Li, Shujuan
AU - Hsu, Ching Cheng
AU - Thet, Suwannee
AU - Kimura, Wataru
AU - Luo, Xiang
AU - Lam, Nicholas T
AU - Menendez-Montes, Ivan
AU - Elhelaly, Waleed M
AU - Cardoso, Alisson Campos
AU - Pereira, Ana Helena Macedo
AU - Singh, Rohit
AU - Sadayappan, Sakthivel
AU - Kanchwala, Mohammed
AU - Xing, Chao
AU - Ladha, Feria A.
AU - Hinson, J. Travis
AU - Hajjar, Roger J.
AU - Hill, Joseph A.
AU - Sadek, Hesham A
N1 - Publisher Copyright:
© 2024 American Heart Association, Inc.
PY - 2024/9/3
Y1 - 2024/9/3
N2 - 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.
AB - 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.
KW - adducin
KW - alpha-actinin
KW - cardiac proliferation
KW - Irak4
KW - sarcomere disassembly
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U2 - 10.1161/CIRCULATIONAHA.122.059102
DO - 10.1161/CIRCULATIONAHA.122.059102
M3 - Article
C2 - 38708635
AN - SCOPUS:85202738555
SN - 0009-7322
VL - 150
SP - 791
EP - 805
JO - Circulation
JF - Circulation
IS - 10
ER -