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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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 |
work_keys_str_mv |
AT claudiasacchetto modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures AT liberovitiello modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures AT leonjdewindt modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures AT alessandrarampazzo modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures AT martinacalore modelingcardiovasculardiseaseswithhipscderivedcardiomyocytesin2dand3dcultures |
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1724648469423980544 |