Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy

Anno: 2020

Autori: Pioner JM., Fornaro A., Coppini R., Ceschia N., Sacconi L., Donati M., Favilli S., Poggesi, C., Olivotto I., Ferrantini C.

Affiliazione autori: Univ Firenze, Dept Expt & Clin Med, Div Physiol, Florence, Italy;‎ Careggi Univ Hosp, Cardiomyopathy Unit, Florence, Italy;‎ Univ Firenze, Dept NeuroFarBa, Florence, Italy; Univ Firenze, LENS, Florence, Italy;‎ CNR, Natl Inst Opt INO, Florence, Italy; A Meyer Childrens Hosp, Metab Unit, Florence, Italy;‎ Meyer Childrens Hosp, Pediat Cardiol, Florence, Italy

Abstract: Familial dilated cardiomyopathy (DCM) is mostly caused by mutations in genes encoding cytoskeletal and sarcomeric proteins. In the pediatric population, DCM is the predominant type of primitive myocardial disease. A severe form of DCM is associated with mutations in the DMD gene encoding dystrophin, which are the cause of Duchenne Muscular Dystrophy (DMD). DMD-associated cardiomyopathy is still poorly understood and orphan of a specific therapy. In the last 5 years, a rise of interest in disease models using human induced pluripotent stem cells (hiPSCs) has led to more than 50 original studies on DCM models. In this review paper, we provide a comprehensive overview on the advances in DMD cardiomyopathy disease modeling and highlight the most remarkable findings obtained from cardiomyocytes differentiated from hiPSCs of DMD patients. We will also describe how hiPSCs based studies have contributed to the identification of specific myocardial disease mechanisms that may be relevant in the pathogenesis of DCM, representing novel potential therapeutic targets.

Giornale/Rivista: FRONTIERS IN PHYSIOLOGY

Volume: 11      Da Pagina: 368-1  A: 368-22

Maggiori informazioni: This work was supported by Fondazione Telethon Italy (GGP16191), Fondazione Telethon-UILDM (GUP19012), 777204/Horizon 2020 (SILICO-FCM project).
Parole chiavi: dilated cardiomyopathy (DCM); duchenne muscular dystrophy (DMD); dystrophin (DMD); hiPSC-cardiomyocyte; stem cell models
DOI: 10.3389/fphys.2020.00368

Citazioni: 8
dati da “WEB OF SCIENCE” (of Thomson Reuters) aggiornati al: 2024-05-19
Riferimenti tratti da Isi Web of Knowledge: (solo abbonati)
Link per visualizzare la scheda su IsiWeb: Clicca qui
Link per visualizzare la citazioni su IsiWeb: Clicca qui