Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures

In the last decade, the generation of cardiac disease models based on human-induced pluripotent stem cells (hiPSCs) has become of common use, providing new opportunities to overcome the lack of appropriate cardiac models. Although much progress has been made toward the generation of hiPSC-derived ca...

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Main Authors: Claudia Sacchetto, Libero Vitiello, Leon J. de Windt, Alessandra Rampazzo, Martina Calore
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/9/3404
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spelling doaj-49611b86f192425fbbb07747c977135f2020-11-25T03:12:47ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-05-01213404340410.3390/ijms21093404Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D CulturesClaudia Sacchetto0Libero Vitiello1Leon J. de Windt2Alessandra Rampazzo3Martina Calore4Department of Molecular Genetics, University of Maastricht, Universiteitssingel 50, 6229ER Maastricht, The NetherlandsDepartment of Biology, University of Padova, via Ugo Bassi 58B, 35131 Padova, ItalyDepartment of Molecular Genetics, University of Maastricht, Universiteitssingel 50, 6229ER Maastricht, The NetherlandsDepartment of Biology, University of Padova, via Ugo Bassi 58B, 35131 Padova, ItalyDepartment of Molecular Genetics, University of Maastricht, Universiteitssingel 50, 6229ER Maastricht, The NetherlandsIn the last decade, the generation of cardiac disease models based on human-induced pluripotent stem cells (hiPSCs) has become of common use, providing new opportunities to overcome the lack of appropriate cardiac models. Although much progress has been made toward the generation of hiPSC-derived cardiomyocytes (hiPS-CMs), several lines of evidence indicate that two-dimensional (2D) cell culturing presents significant limitations, including hiPS-CMs immaturity and the absence of interaction between different cell types and the extracellular matrix. More recently, new advances in bioengineering and co-culture systems have allowed the generation of three-dimensional (3D) constructs based on hiPSC-derived cells. Within these systems, biochemical and physical stimuli influence the maturation of hiPS-CMs, which can show structural and functional properties more similar to those present in adult cardiomyocytes. In this review, we describe the latest advances in 2D- and 3D-hiPSC technology for cardiac disease mechanisms investigation, drug development, and therapeutic studies.https://www.mdpi.com/1422-0067/21/9/3404cardiac disease modelinghuman induced pluripotent stem cells3D cardiac modelsengineered heart tissue
collection DOAJ
language English
format Article
sources DOAJ
author Claudia Sacchetto
Libero Vitiello
Leon J. de Windt
Alessandra Rampazzo
Martina Calore
spellingShingle Claudia Sacchetto
Libero Vitiello
Leon J. de Windt
Alessandra Rampazzo
Martina Calore
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
International Journal of Molecular Sciences
cardiac disease modeling
human induced pluripotent stem cells
3D cardiac models
engineered heart tissue
author_facet Claudia Sacchetto
Libero Vitiello
Leon J. de Windt
Alessandra Rampazzo
Martina Calore
author_sort Claudia Sacchetto
title Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
title_short Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
title_full Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
title_fullStr Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
title_full_unstemmed Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures
title_sort modeling cardiovascular diseases with hipsc-derived cardiomyocytes in 2d and 3d cultures
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-05-01
description In the last decade, the generation of cardiac disease models based on human-induced pluripotent stem cells (hiPSCs) has become of common use, providing new opportunities to overcome the lack of appropriate cardiac models. Although much progress has been made toward the generation of hiPSC-derived cardiomyocytes (hiPS-CMs), several lines of evidence indicate that two-dimensional (2D) cell culturing presents significant limitations, including hiPS-CMs immaturity and the absence of interaction between different cell types and the extracellular matrix. More recently, new advances in bioengineering and co-culture systems have allowed the generation of three-dimensional (3D) constructs based on hiPSC-derived cells. Within these systems, biochemical and physical stimuli influence the maturation of hiPS-CMs, which can show structural and functional properties more similar to those present in adult cardiomyocytes. In this review, we describe the latest advances in 2D- and 3D-hiPSC technology for cardiac disease mechanisms investigation, drug development, and therapeutic studies.
topic cardiac disease modeling
human induced pluripotent stem cells
3D cardiac models
engineered heart tissue
url https://www.mdpi.com/1422-0067/21/9/3404
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AT liberovitiello modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures
AT leonjdewindt modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures
AT alessandrarampazzo modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures
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