BioTalentum Ltd., Aulich Lajos Str 26, H-2100 Gödöllő, Hungary.
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.
Int J Mol Sci. 2024 Aug 24;25(17):9186. doi: 10.3390/ijms25179186.
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.
心血管研究领域存在众多悬而未决的难题,其中之一就是缺乏妥协性的体外心脏模型。虽然动物模型的原代细胞来源具有优势和劣势,但过去半个世纪以来,人们一直致力于减少其使用。此外,获得足够数量的人类原代心肌细胞还面临着伦理和法律方面的挑战。由于诱导多能干细胞(hiPSC-CM)作为人类心肌细胞的近乎无限的来源已基本得到解决,因此人们正在努力通过克服其内在局限性来提高其质量和适用性。该领域最大的瓶颈是 hiPSC-CM 的体外老化,使其达到与成人心脏非常相似的成熟状态,从而可以进行更合适的药物研发程序,因为衰老和心血管疾病的发展之间存在明显的相关性。在这里,我们综述了在疾病建模和毒性评估中使用的最逼真的心脏模型,从 hiPSC-CM 成熟到基于芯片的心脏平台和计算机模型,再到某些心血管疾病的体外模型,介绍了当前最先进的技术。