Adducin Regulates Sarcomere Disassembly During Cardiomyocyte Mitosis

Author:

Xiao Feng1,Nguyen Ngoc Uyen Nhi1ORCID,Wang Ping1,Li Shujuan1,Hsu Ching-Cheng1,Thet Suwannee1,Kimura Wataru12ORCID,Luo Xiang1ORCID,Lam Nicholas T.1,Menendez-Montes Ivan1,Elhelaly Waleed M.1ORCID,Cardoso Alisson Campos13ORCID,Pereira Ana Helena Macedo13,Singh Rohit45,Sadayappan Sakthivel4ORCID,Kanchwala Mohammed6ORCID,Xing Chao678ORCID,Ladha Feria A.9ORCID,Hinson J. Travis1910ORCID,Hajjar Roger J.11ORCID,Hill Joseph A.1213ORCID,Sadek Hesham A.113141516ORCID

Affiliation:

1. Department of Internal Medicine (Cardiology) (F.X., N.U.N.N., P.W., S.L., C.-C.H., S.T., W.K., X.L., N.T.L., I.M.-M., W.M.E., A.C.C., A.H.M.P., J.A.H., H.A.S.), University of Texas Southwestern Medical Center, Dallas.

2. Life Science Center, Tsukuba Advanced Research Alliance, University of Tsukuba, Japan (W.K.).

3. Biosciences National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas (A.C.C., A.H.M.P.).

4. Center for Cardiovascular Research, Division of Cardiovascular Health and Disease, Department of Internal Medicine, University of Cincinnati College of Medicine, OH (R.S., S.S.).

5. Amgen Research, Department of Cardiometabolic Disorders, Amgen, South San Francisco, CA (R.S.).

6. Eugene McDermott Center for Human Growth and Development (M.K., C.X.), University of Texas Southwestern Medical Center, Dallas.

7. Lyda Hill Department of Bioinformatics (C.X.), University of Texas Southwestern Medical Center, Dallas.

8. O’Donnell School of Public Health (C.X.), University of Texas Southwestern Medical Center, Dallas.

9. University of Connecticut Health Center, Farmington (F.A.L., J.T.H.).

10. Jackson Laboratory for Genomic Medicine, Farmington, CT (J.T.H.).

11. Gene & Cell Therapy Institute, Mass General Brigham, Cambridge, MA (R.J.H.).

12. Moss Heart Center (J.A.H.), University of Texas Southwestern Medical Center, Dallas.

13. Department of Molecular Biology (J.A.H., H.A.S.), University of Texas Southwestern Medical Center, Dallas.

14. Department of Biophysics (H.A.S.), University of Texas Southwestern Medical Center, Dallas.

15. Hamon Center for Regenerative Science and Medicine (H.A.S.), University of Texas Southwestern Medical Center, Dallas.

16. Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain (H.A.S.).

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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