Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation

The stem cell technology and the induced pluripotent stem cells (iPSCs) production represent an excellent alternative tool to study cardiomyopathies, which overcome the limitations associated with primary cardiomyocytes (CMs) access and manipulation. CMs from human iPSCs (hiPSC–CMs) are genetically...

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Main Authors: Francesco Lodola, Verónica Celeste De Giusti, Claudia Maniezzi, Daniele Martone, Ilaria Stadiotti, Elena Sommariva, Angela Serena Maione
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Biology
Subjects:
Online Access:https://www.mdpi.com/2079-7737/10/8/730
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author Francesco Lodola
Verónica Celeste De Giusti
Claudia Maniezzi
Daniele Martone
Ilaria Stadiotti
Elena Sommariva
Angela Serena Maione
author_facet Francesco Lodola
Verónica Celeste De Giusti
Claudia Maniezzi
Daniele Martone
Ilaria Stadiotti
Elena Sommariva
Angela Serena Maione
author_sort Francesco Lodola
collection DOAJ
description The stem cell technology and the induced pluripotent stem cells (iPSCs) production represent an excellent alternative tool to study cardiomyopathies, which overcome the limitations associated with primary cardiomyocytes (CMs) access and manipulation. CMs from human iPSCs (hiPSC–CMs) are genetically identical to patient primary cells of origin, with the main electrophysiological and mechanical features of CMs. The key issue to be solved is to achieve a degree of structural and functional maturity typical of adult CMs. In this perspective, we will focus on the main differences between fetal-like hiPSC-CMs and adult CMs. A viewpoint is given on the different approaches used to improve hiPSC-CMs maturity, spanning from long-term culture to complex engineered heart tissue. Further, we outline limitations and future developments needed in cardiomyopathy disease modeling.
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spelling doaj.art-490e122b730f4b499edb7f68985ec0362023-11-22T06:49:43ZengMDPI AGBiology2079-77372021-07-0110873010.3390/biology10080730Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes MaturationFrancesco Lodola0Verónica Celeste De Giusti1Claudia Maniezzi2Daniele Martone3Ilaria Stadiotti4Elena Sommariva5Angela Serena Maione6Department of Biotechnology and Biosciences, University of Milano-Bicocca, Piazza della Scienza, 2, Ed U3, 20126 Milan, ItalyCentro de Investigaciones Cardiovasculares, Facultad de Ciencias Médicas, Universidad Nacional de La Plata-CONICET, La Plata 1900, ArgentinaDepartment of Biotechnology and Biosciences, University of Milano-Bicocca, Piazza della Scienza, 2, Ed U3, 20126 Milan, ItalyDepartment of Biotechnology and Biosciences, University of Milano-Bicocca, Piazza della Scienza, 2, Ed U3, 20126 Milan, ItalyVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, 20138 Milan, ItalyVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, 20138 Milan, ItalyVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, 20138 Milan, ItalyThe stem cell technology and the induced pluripotent stem cells (iPSCs) production represent an excellent alternative tool to study cardiomyopathies, which overcome the limitations associated with primary cardiomyocytes (CMs) access and manipulation. CMs from human iPSCs (hiPSC–CMs) are genetically identical to patient primary cells of origin, with the main electrophysiological and mechanical features of CMs. The key issue to be solved is to achieve a degree of structural and functional maturity typical of adult CMs. In this perspective, we will focus on the main differences between fetal-like hiPSC-CMs and adult CMs. A viewpoint is given on the different approaches used to improve hiPSC-CMs maturity, spanning from long-term culture to complex engineered heart tissue. Further, we outline limitations and future developments needed in cardiomyopathy disease modeling.https://www.mdpi.com/2079-7737/10/8/730hiPSC-CMscardiomyopathiescardiovascular disease modelingpatient-specific medicinestem cell maturation
spellingShingle Francesco Lodola
Verónica Celeste De Giusti
Claudia Maniezzi
Daniele Martone
Ilaria Stadiotti
Elena Sommariva
Angela Serena Maione
Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
Biology
hiPSC-CMs
cardiomyopathies
cardiovascular disease modeling
patient-specific medicine
stem cell maturation
title Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
title_full Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
title_fullStr Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
title_full_unstemmed Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
title_short Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
title_sort modeling cardiomyopathies in a dish state of the art and novel perspectives on hipsc derived cardiomyocytes maturation
topic hiPSC-CMs
cardiomyopathies
cardiovascular disease modeling
patient-specific medicine
stem cell maturation
url https://www.mdpi.com/2079-7737/10/8/730
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