The Current State of Realistic Heart Models for Disease Modelling and Cardiotoxicity

Author:

Kistamás Kornél1ORCID,Lamberto Federica12ORCID,Vaiciuleviciute Raminta3ORCID,Leal Filipa4,Muenthaisong Suchitra1,Marte Luis5ORCID,Subías-Beltrán Paula5ORCID,Alaburda Aidas36ORCID,Arvanitis Dina N.7,Zana Melinda1ORCID,Costa Pedro F.4ORCID,Bernotiene Eiva38,Bergaud Christian7,Dinnyés András12ORCID

Affiliation:

1. BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary

2. Department of Physiology and Animal Health, Institute of Physiology and Animal Nutrition, Hungarian University of Agriculture and Life Sciences, Páter Károly Str 1, H-2100 Gödöllő, Hungary

3. Department of Regenerative Medicine, State Research Institute Innovative Medicine Centre, Santariskiu g. 5, LT-08406 Vilnius, Lithuania

4. Biofabics Lda, Rua Alfredo Allen 455, 4200-135 Porto, Portugal

5. Digital Health Unit, Eurecat—Centre Tecnològic de Catalunya, 08005 Barcelona, Spain

6. Institute of Biosciences, Life Sciences Center, Vilnius University, Sauletekio al. 7, LT-10257 Vilnius, Lithuania

7. Laboratory for Analysis and Architecture of Systems—French National Centre for Scientific Research (LAAS-CNRS), 7 Avenue du Colonel Roche, F-31400 Toulouse, France

8. Faculty of Fundamental Sciences, Vilnius Tech, Sauletekio al. 11, LT-10223 Vilnius, Lithuania

Abstract

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.

Funder

EU Horizon 2020

National Research, Development and Innovation Fund

Hungarian Ministry for National Economy for the IPCEI Med4Cure “Cardiabetter” project

Publisher

MDPI AG

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