Scheurer Fabian, Hammer Alexander, Schubert Mario, Steiner Robert-Patrick, Gamm Oliver, Guan Kaomei, Sonntag Frank, Malberg Hagen, Schmidt Martin
Institute of Biomedical Engineering, TU Dresden, Fetscherstr. 29, Dresden 01307, Germany.
Fraunhofer Institute for Material and Beam Technology IWS, Winterbergstr. 28, Dresden 01277, Germany.
Comput Struct Biotechnol J. 2025 Aug 22;27:3719-3728. doi: 10.1016/j.csbj.2025.08.024. eCollection 2025.
Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) are an important resource for identifying novel therapeutic targets and cardioprotective drugs. However, a key limitation of iPSC-CMs is their immature, fetal-like phenotype. Cultivation of iPSC-CMs in lipid-supplemented maturation media (MM) enhances the structural, metabolic and electrophysiological properties of iPSC-CMs. Nevertheless, they face substantial limitations as there are labor-intensive, time consuming and go in line with cell damage or loss of the sample. To address this issue, we have developed a non-invasive approach for automated classification of iPSC-CM maturity through interpretable artificial intelligence (AI)-based analysis of beat characteristics derived from video-based motion analysis. In a prospective study, we evaluated 230 video recordings of early-state, immature iPSC-CMs on day 21 after differentiation (d21) and more mature iPSC-CMs cultured in MM (d42, MM). For each recording, 10 features were extracted using Maia motion analysis software and entered into a support vector machine (SVM). The hyperparameters of the SVM were optimized in a grid search on 80 % of the data using 5-fold cross-validation. The optimized model achieved an accuracy of 99.5 ± 1.1 % on a hold-out test set. Shapley Additive Explanations (SHAP) identified displacement, relaxation-rise time and beating duration as the most relevant features for assessing iPSC-CM maturity. Our results suggest the use of non-invasive, optical motion analysis combined with AI-based methods as a tool to assess iPSC-CMs maturity and could be applied before performing functional readouts or drug testing. This may potentially reduce the variability and improve the reproducibility of experimental studies.
人诱导多能干细胞衍生的心肌细胞(iPSC-CMs)是识别新型治疗靶点和心脏保护药物的重要资源。然而,iPSC-CMs的一个关键局限性是它们具有不成熟的胎儿样表型。在添加脂质的成熟培养基(MM)中培养iPSC-CMs可增强其结构、代谢和电生理特性。尽管如此,它们仍面临重大限制,因为这需要大量人力、耗时,且会导致细胞损伤或样本丢失。为了解决这个问题,我们开发了一种非侵入性方法,通过基于可解释人工智能(AI)的视频运动分析得出的搏动特征分析,对iPSC-CM的成熟度进行自动分类。在一项前瞻性研究中,我们评估了分化后第21天(d21)的早期未成熟iPSC-CMs和在MM中培养的更成熟iPSC-CMs(d42,MM)的230个视频记录。对于每个记录,使用Maia运动分析软件提取10个特征,并输入支持向量机(SVM)。SVM的超参数在使用5折交叉验证的80%数据的网格搜索中进行了优化。优化后的模型在保留测试集上的准确率达到了99.5±1.1%。Shapley加法解释(SHAP)确定位移、松弛上升时间和搏动持续时间是评估iPSC-CM成熟度最相关的特征。我们的结果表明,使用非侵入性光学运动分析结合基于AI的方法作为评估iPSC-CMs成熟度的工具,可在进行功能读数或药物测试之前应用。这可能会减少变异性并提高实验研究的可重复性。