The Current State of Realistic Heart Models for Disease Modelling and Cardiotoxicity.
Kornél Kistamás, Federica Lamberto, Raminta Vaiciuleviciute, Filipa Leal, Suchitra Muenthaisong, Luis Marte, Paula Subías-Beltrán, Aidas Alaburda, Dina N Arvanitis, Melinda Zana, Pedro F Costa, Eiva Bernotiene, Christian Bergaud, András Dinnyés
Author Information
Kornél Kistamás: BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary. ORCID
Federica Lamberto: BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary. ORCID
Raminta Vaiciuleviciute: Department of Regenerative Medicine, State Research Institute Innovative Medicine Centre, Santariskiu g. 5, LT-08406 Vilnius, Lithuania. ORCID
Filipa Leal: Biofabics Lda, Rua Alfredo Allen 455, 4200-135 Porto, Portugal.
Suchitra Muenthaisong: BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary.
Luis Marte: Digital Health Unit, Eurecat-Centre Tecnològic de Catalunya, 08005 Barcelona, Spain. ORCID
Paula Subías-Beltrán: Digital Health Unit, Eurecat-Centre Tecnològic de Catalunya, 08005 Barcelona, Spain. ORCID
Aidas Alaburda: Department of Regenerative Medicine, State Research Institute Innovative Medicine Centre, Santariskiu g. 5, LT-08406 Vilnius, Lithuania. ORCID
Dina N Arvanitis: Laboratory for Analysis and Architecture of Systems-French National Centre for Scientific Research (LAAS-CNRS), 7 Avenue du Colonel Roche, F-31400 Toulouse, France.
Melinda Zana: BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary. ORCID
Pedro F Costa: Biofabics Lda, Rua Alfredo Allen 455, 4200-135 Porto, Portugal. ORCID
Eiva Bernotiene: Department of Regenerative Medicine, State Research Institute Innovative Medicine Centre, Santariskiu g. 5, LT-08406 Vilnius, Lithuania.
Christian Bergaud: Laboratory for Analysis and Architecture of Systems-French National Centre for Scientific Research (LAAS-CNRS), 7 Avenue du Colonel Roche, F-31400 Toulouse, France.
András Dinnyés: BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary. ORCID
中文译文
English
One of the many unresolved obstacles in the field of cardiovascular research is an uncompromising in vitro cardiac model. While primary cell sources from animal models offer both advantages and disadvantages, efforts over the past half-century have aimed to reduce their use. Additionally, obtaining a sufficient quantity of human primary cardiomyocytes faces ethical and legal challenges. As the practically unlimited source of human cardiomyocytes from induced pluripotent stem cells (hiPSC-CM) is now mostly resolved, there are great efforts to improve their quality and applicability by overcoming their intrinsic limitations. The greatest bottleneck in the field is the in vitro ageing of hiPSC-CMs to reach a maturity status that closely resembles that of the adult heart, thereby allowing for more appropriate drug developmental procedures as there is a clear correlation between ageing and developing cardiovascular diseases. Here, we review the current state-of-the-art techniques in the most realistic heart models used in disease modelling and toxicity evaluations from hiPSC-CM maturation through heart-on-a-chip platforms and in silico models to the in vitro models of certain cardiovascular diseases.
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No. 953138/EU Horizon 2020
No. 812660/EU Horizon 2020
No. 2020-1.1.5-GYORSÍTÓSÁV-2021-00016/Hungarian National Research, Development and Innovation Fund
Humans
Cardiotoxicity
Induced Pluripotent Stem Cells
Myocytes, Cardiac
Animals
Cell Differentiation
Cardiovascular Diseases
Models, Cardiovascular